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+ <Contact-Ref ref="contrib1" />
259
+ <Supplementary-Data type="IDAT">
260
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739721/suppl/GSM2739721_3999356083_R01C01_Grn.idat.gz
261
+ </Supplementary-Data>
262
+ <Supplementary-Data type="IDAT">
263
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739721/suppl/GSM2739721_3999356083_R01C01_Red.idat.gz
264
+ </Supplementary-Data>
265
+ <Data-Table>
266
+ <Column position="1">
267
+ <Name>ID_REF</Name>
268
+ </Column>
269
+ <Column position="2">
270
+ <Name>VALUE</Name>
271
+ <Description>Average Beta non-normalized Beta</Description>
272
+ </Column>
273
+ <Column position="3">
274
+ <Name>Detection Pval</Name>
275
+ </Column>
276
+ <External-Data rows="467971">
277
+ GSM2739721-tbl-1.txt
278
+ </External-Data>
279
+ </Data-Table>
280
+ </Sample>
281
+
282
+ <Sample iid="GSM2739722">
283
+ <Status database="GEO">
284
+ <Submission-Date>2017-08-10</Submission-Date>
285
+ <Release-Date>2017-12-31</Release-Date>
286
+ <Last-Update-Date>2018-01-23</Last-Update-Date>
287
+ </Status>
288
+ <Title>PBMC Genomic DNA G00041</Title>
289
+ <Accession database="GEO">GSM2739722</Accession>
290
+ <Type>genomic</Type>
291
+ <Channel-Count>1</Channel-Count>
292
+ <Channel position="1">
293
+ <Source>PBMC</Source>
294
+ <Organism taxid="9606">Homo sapiens</Organism>
295
+ <Characteristics tag="Sex">
296
+ female
297
+ </Characteristics>
298
+ <Characteristics tag="disease state">
299
+ CFS
300
+ </Characteristics>
301
+ <Molecule>genomic DNA</Molecule>
302
+ <Extract-Protocol>
303
+ Genomic DNA was extracted and purified from Omega EZNA Tissue DNA Kit according to manufacturer's instructions
304
+ </Extract-Protocol>
305
+ <Label>Cy3 and Cy5</Label>
306
+ <Label-Protocol>
307
+ Standard Illumina Protocol
308
+ </Label-Protocol>
309
+ </Channel>
310
+ <Hybridization-Protocol>
311
+ Bisulfite converted DNA was amplified, fragmented and hybridised to Illumina Infinium Human Methylation450 Beadchip using standard Illumina protocol
312
+ </Hybridization-Protocol>
313
+ <Scan-Protocol>
314
+ Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting
315
+ </Scan-Protocol>
316
+ <Description>
317
+ CFS Genomic DNA
318
+ </Description>
319
+ <Data-Processing>
320
+ BeadStudio software v3.2
321
+ </Data-Processing>
322
+ <Platform-Ref ref="GPL13534" />
323
+ <Contact-Ref ref="contrib1" />
324
+ <Supplementary-Data type="IDAT">
325
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739722/suppl/GSM2739722_3999356083_R02C01_Grn.idat.gz
326
+ </Supplementary-Data>
327
+ <Supplementary-Data type="IDAT">
328
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739722/suppl/GSM2739722_3999356083_R02C01_Red.idat.gz
329
+ </Supplementary-Data>
330
+ <Data-Table>
331
+ <Column position="1">
332
+ <Name>ID_REF</Name>
333
+ </Column>
334
+ <Column position="2">
335
+ <Name>VALUE</Name>
336
+ <Description>Average Beta non-normalized Beta</Description>
337
+ </Column>
338
+ <Column position="3">
339
+ <Name>Detection Pval</Name>
340
+ </Column>
341
+ <External-Data rows="467971">
342
+ GSM2739722-tbl-1.txt
343
+ </External-Data>
344
+ </Data-Table>
345
+ </Sample>
346
+
347
+ <Sample iid="GSM2739723">
348
+ <Status database="GEO">
349
+ <Submission-Date>2017-08-10</Submission-Date>
350
+ <Release-Date>2017-12-31</Release-Date>
351
+ <Last-Update-Date>2018-01-23</Last-Update-Date>
352
+ </Status>
353
+ <Title>PBMC Genomic DNA G00043</Title>
354
+ <Accession database="GEO">GSM2739723</Accession>
355
+ <Type>genomic</Type>
356
+ <Channel-Count>1</Channel-Count>
357
+ <Channel position="1">
358
+ <Source>PBMC</Source>
359
+ <Organism taxid="9606">Homo sapiens</Organism>
360
+ <Characteristics tag="Sex">
361
+ female
362
+ </Characteristics>
363
+ <Characteristics tag="disease state">
364
+ CFS
365
+ </Characteristics>
366
+ <Molecule>genomic DNA</Molecule>
367
+ <Extract-Protocol>
368
+ Genomic DNA was extracted and purified from Omega EZNA Tissue DNA Kit according to manufacturer's instructions
369
+ </Extract-Protocol>
370
+ <Label>Cy3 and Cy5</Label>
371
+ <Label-Protocol>
372
+ Standard Illumina Protocol
373
+ </Label-Protocol>
374
+ </Channel>
375
+ <Hybridization-Protocol>
376
+ Bisulfite converted DNA was amplified, fragmented and hybridised to Illumina Infinium Human Methylation450 Beadchip using standard Illumina protocol
377
+ </Hybridization-Protocol>
378
+ <Scan-Protocol>
379
+ Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting
380
+ </Scan-Protocol>
381
+ <Description>
382
+ CFS Genomic DNA
383
+ </Description>
384
+ <Data-Processing>
385
+ BeadStudio software v3.2
386
+ </Data-Processing>
387
+ <Platform-Ref ref="GPL13534" />
388
+ <Contact-Ref ref="contrib1" />
389
+ <Supplementary-Data type="IDAT">
390
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739723/suppl/GSM2739723_3999356083_R03C01_Grn.idat.gz
391
+ </Supplementary-Data>
392
+ <Supplementary-Data type="IDAT">
393
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739723/suppl/GSM2739723_3999356083_R03C01_Red.idat.gz
394
+ </Supplementary-Data>
395
+ <Data-Table>
396
+ <Column position="1">
397
+ <Name>ID_REF</Name>
398
+ </Column>
399
+ <Column position="2">
400
+ <Name>VALUE</Name>
401
+ <Description>Average Beta non-normalized Beta</Description>
402
+ </Column>
403
+ <Column position="3">
404
+ <Name>Detection Pval</Name>
405
+ </Column>
406
+ <External-Data rows="467971">
407
+ GSM2739723-tbl-1.txt
408
+ </External-Data>
409
+ </Data-Table>
410
+ </Sample>
411
+
412
+ <Sample iid="GSM2739724">
413
+ <Status database="GEO">
414
+ <Submission-Date>2017-08-10</Submission-Date>
415
+ <Release-Date>2017-12-31</Release-Date>
416
+ <Last-Update-Date>2018-01-23</Last-Update-Date>
417
+ </Status>
418
+ <Title>PBMC Genomic DNA G00052</Title>
419
+ <Accession database="GEO">GSM2739724</Accession>
420
+ <Type>genomic</Type>
421
+ <Channel-Count>1</Channel-Count>
422
+ <Channel position="1">
423
+ <Source>PBMC</Source>
424
+ <Organism taxid="9606">Homo sapiens</Organism>
425
+ <Characteristics tag="Sex">
426
+ female
427
+ </Characteristics>
428
+ <Characteristics tag="disease state">
429
+ CFS
430
+ </Characteristics>
431
+ <Molecule>genomic DNA</Molecule>
432
+ <Extract-Protocol>
433
+ Genomic DNA was extracted and purified from Omega EZNA Tissue DNA Kit according to manufacturer's instructions
434
+ </Extract-Protocol>
435
+ <Label>Cy3 and Cy5</Label>
436
+ <Label-Protocol>
437
+ Standard Illumina Protocol
438
+ </Label-Protocol>
439
+ </Channel>
440
+ <Hybridization-Protocol>
441
+ Bisulfite converted DNA was amplified, fragmented and hybridised to Illumina Infinium Human Methylation450 Beadchip using standard Illumina protocol
442
+ </Hybridization-Protocol>
443
+ <Scan-Protocol>
444
+ Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting
445
+ </Scan-Protocol>
446
+ <Description>
447
+ CFS Genomic DNA
448
+ </Description>
449
+ <Data-Processing>
450
+ BeadStudio software v3.2
451
+ </Data-Processing>
452
+ <Platform-Ref ref="GPL13534" />
453
+ <Contact-Ref ref="contrib1" />
454
+ <Supplementary-Data type="IDAT">
455
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739724/suppl/GSM2739724_3999356083_R04C01_Grn.idat.gz
456
+ </Supplementary-Data>
457
+ <Supplementary-Data type="IDAT">
458
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739724/suppl/GSM2739724_3999356083_R04C01_Red.idat.gz
459
+ </Supplementary-Data>
460
+ <Data-Table>
461
+ <Column position="1">
462
+ <Name>ID_REF</Name>
463
+ </Column>
464
+ <Column position="2">
465
+ <Name>VALUE</Name>
466
+ <Description>Average Beta non-normalized Beta</Description>
467
+ </Column>
468
+ <Column position="3">
469
+ <Name>Detection Pval</Name>
470
+ </Column>
471
+ <External-Data rows="467971">
472
+ GSM2739724-tbl-1.txt
473
+ </External-Data>
474
+ </Data-Table>
475
+ </Sample>
476
+
477
+ <Sample iid="GSM2739725">
478
+ <Status database="GEO">
479
+ <Submission-Date>2017-08-10</Submission-Date>
480
+ <Release-Date>2017-12-31</Release-Date>
481
+ <Last-Update-Date>2018-01-23</Last-Update-Date>
482
+ </Status>
483
+ <Title>PBMC Genomic DNA G00069</Title>
484
+ <Accession database="GEO">GSM2739725</Accession>
485
+ <Type>genomic</Type>
486
+ <Channel-Count>1</Channel-Count>
487
+ <Channel position="1">
488
+ <Source>PBMC</Source>
489
+ <Organism taxid="9606">Homo sapiens</Organism>
490
+ <Characteristics tag="Sex">
491
+ female
492
+ </Characteristics>
493
+ <Characteristics tag="disease state">
494
+ CFS
495
+ </Characteristics>
496
+ <Molecule>genomic DNA</Molecule>
497
+ <Extract-Protocol>
498
+ Genomic DNA was extracted and purified from Omega EZNA Tissue DNA Kit according to manufacturer's instructions
499
+ </Extract-Protocol>
500
+ <Label>Cy3 and Cy5</Label>
501
+ <Label-Protocol>
502
+ Standard Illumina Protocol
503
+ </Label-Protocol>
504
+ </Channel>
505
+ <Hybridization-Protocol>
506
+ Bisulfite converted DNA was amplified, fragmented and hybridised to Illumina Infinium Human Methylation450 Beadchip using standard Illumina protocol
507
+ </Hybridization-Protocol>
508
+ <Scan-Protocol>
509
+ Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting
510
+ </Scan-Protocol>
511
+ <Description>
512
+ CFS Genomic DNA
513
+ </Description>
514
+ <Data-Processing>
515
+ BeadStudio software v3.2
516
+ </Data-Processing>
517
+ <Platform-Ref ref="GPL13534" />
518
+ <Contact-Ref ref="contrib1" />
519
+ <Supplementary-Data type="IDAT">
520
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739725/suppl/GSM2739725_3999356083_R06C01_Grn.idat.gz
521
+ </Supplementary-Data>
522
+ <Supplementary-Data type="IDAT">
523
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739725/suppl/GSM2739725_3999356083_R06C01_Red.idat.gz
524
+ </Supplementary-Data>
525
+ <Data-Table>
526
+ <Column position="1">
527
+ <Name>ID_REF</Name>
528
+ </Column>
529
+ <Column position="2">
530
+ <Name>VALUE</Name>
531
+ <Description>Average Beta non-normalized Beta</Description>
532
+ </Column>
533
+ <Column position="3">
534
+ <Name>Detection Pval</Name>
535
+ </Column>
536
+ <External-Data rows="467971">
537
+ GSM2739725-tbl-1.txt
538
+ </External-Data>
539
+ </Data-Table>
540
+ </Sample>
541
+
542
+ <Sample iid="GSM2739726">
543
+ <Status database="GEO">
544
+ <Submission-Date>2017-08-10</Submission-Date>
545
+ <Release-Date>2017-12-31</Release-Date>
546
+ <Last-Update-Date>2018-01-23</Last-Update-Date>
547
+ </Status>
548
+ <Title>PBMC Genomic DNA G00074</Title>
549
+ <Accession database="GEO">GSM2739726</Accession>
550
+ <Type>genomic</Type>
551
+ <Channel-Count>1</Channel-Count>
552
+ <Channel position="1">
553
+ <Source>PBMC</Source>
554
+ <Organism taxid="9606">Homo sapiens</Organism>
555
+ <Characteristics tag="Sex">
556
+ female
557
+ </Characteristics>
558
+ <Characteristics tag="disease state">
559
+ CFS
560
+ </Characteristics>
561
+ <Molecule>genomic DNA</Molecule>
562
+ <Extract-Protocol>
563
+ Genomic DNA was extracted and purified from Omega EZNA Tissue DNA Kit according to manufacturer's instructions
564
+ </Extract-Protocol>
565
+ <Label>Cy3 and Cy5</Label>
566
+ <Label-Protocol>
567
+ Standard Illumina Protocol
568
+ </Label-Protocol>
569
+ </Channel>
570
+ <Hybridization-Protocol>
571
+ Bisulfite converted DNA was amplified, fragmented and hybridised to Illumina Infinium Human Methylation450 Beadchip using standard Illumina protocol
572
+ </Hybridization-Protocol>
573
+ <Scan-Protocol>
574
+ Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting
575
+ </Scan-Protocol>
576
+ <Description>
577
+ CFS Genomic DNA
578
+ </Description>
579
+ <Data-Processing>
580
+ BeadStudio software v3.2
581
+ </Data-Processing>
582
+ <Platform-Ref ref="GPL13534" />
583
+ <Contact-Ref ref="contrib1" />
584
+ <Supplementary-Data type="IDAT">
585
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739726/suppl/GSM2739726_3999356083_R05C01_Grn.idat.gz
586
+ </Supplementary-Data>
587
+ <Supplementary-Data type="IDAT">
588
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739726/suppl/GSM2739726_3999356083_R05C01_Red.idat.gz
589
+ </Supplementary-Data>
590
+ <Data-Table>
591
+ <Column position="1">
592
+ <Name>ID_REF</Name>
593
+ </Column>
594
+ <Column position="2">
595
+ <Name>VALUE</Name>
596
+ <Description>Average Beta non-normalized Beta</Description>
597
+ </Column>
598
+ <Column position="3">
599
+ <Name>Detection Pval</Name>
600
+ </Column>
601
+ <External-Data rows="467971">
602
+ GSM2739726-tbl-1.txt
603
+ </External-Data>
604
+ </Data-Table>
605
+ </Sample>
606
+
607
+ <Sample iid="GSM2739727">
608
+ <Status database="GEO">
609
+ <Submission-Date>2017-08-10</Submission-Date>
610
+ <Release-Date>2017-12-31</Release-Date>
611
+ <Last-Update-Date>2018-01-23</Last-Update-Date>
612
+ </Status>
613
+ <Title>PBMC Genomic DNA G00077</Title>
614
+ <Accession database="GEO">GSM2739727</Accession>
615
+ <Type>genomic</Type>
616
+ <Channel-Count>1</Channel-Count>
617
+ <Channel position="1">
618
+ <Source>PBMC</Source>
619
+ <Organism taxid="9606">Homo sapiens</Organism>
620
+ <Characteristics tag="Sex">
621
+ female
622
+ </Characteristics>
623
+ <Characteristics tag="disease state">
624
+ CFS
625
+ </Characteristics>
626
+ <Molecule>genomic DNA</Molecule>
627
+ <Extract-Protocol>
628
+ Genomic DNA was extracted and purified from Omega EZNA Tissue DNA Kit according to manufacturer's instructions
629
+ </Extract-Protocol>
630
+ <Label>Cy3 and Cy5</Label>
631
+ <Label-Protocol>
632
+ Standard Illumina Protocol
633
+ </Label-Protocol>
634
+ </Channel>
635
+ <Hybridization-Protocol>
636
+ Bisulfite converted DNA was amplified, fragmented and hybridised to Illumina Infinium Human Methylation450 Beadchip using standard Illumina protocol
637
+ </Hybridization-Protocol>
638
+ <Scan-Protocol>
639
+ Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting
640
+ </Scan-Protocol>
641
+ <Description>
642
+ CFS Genomic DNA
643
+ </Description>
644
+ <Data-Processing>
645
+ BeadStudio software v3.2
646
+ </Data-Processing>
647
+ <Platform-Ref ref="GPL13534" />
648
+ <Contact-Ref ref="contrib1" />
649
+ <Supplementary-Data type="IDAT">
650
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739727/suppl/GSM2739727_3999356082_R01C01_Grn.idat.gz
651
+ </Supplementary-Data>
652
+ <Supplementary-Data type="IDAT">
653
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739727/suppl/GSM2739727_3999356082_R01C01_Red.idat.gz
654
+ </Supplementary-Data>
655
+ <Data-Table>
656
+ <Column position="1">
657
+ <Name>ID_REF</Name>
658
+ </Column>
659
+ <Column position="2">
660
+ <Name>VALUE</Name>
661
+ <Description>Average Beta non-normalized Beta</Description>
662
+ </Column>
663
+ <Column position="3">
664
+ <Name>Detection Pval</Name>
665
+ </Column>
666
+ <External-Data rows="467971">
667
+ GSM2739727-tbl-1.txt
668
+ </External-Data>
669
+ </Data-Table>
670
+ </Sample>
671
+
672
+ <Sample iid="GSM2739728">
673
+ <Status database="GEO">
674
+ <Submission-Date>2017-08-10</Submission-Date>
675
+ <Release-Date>2017-12-31</Release-Date>
676
+ <Last-Update-Date>2018-01-23</Last-Update-Date>
677
+ </Status>
678
+ <Title>PBMC Genomic DNA G00100</Title>
679
+ <Accession database="GEO">GSM2739728</Accession>
680
+ <Type>genomic</Type>
681
+ <Channel-Count>1</Channel-Count>
682
+ <Channel position="1">
683
+ <Source>PBMC</Source>
684
+ <Organism taxid="9606">Homo sapiens</Organism>
685
+ <Characteristics tag="Sex">
686
+ female
687
+ </Characteristics>
688
+ <Characteristics tag="disease state">
689
+ CFS
690
+ </Characteristics>
691
+ <Molecule>genomic DNA</Molecule>
692
+ <Extract-Protocol>
693
+ Genomic DNA was extracted and purified from Omega EZNA Tissue DNA Kit according to manufacturer's instructions
694
+ </Extract-Protocol>
695
+ <Label>Cy3 and Cy5</Label>
696
+ <Label-Protocol>
697
+ Standard Illumina Protocol
698
+ </Label-Protocol>
699
+ </Channel>
700
+ <Hybridization-Protocol>
701
+ Bisulfite converted DNA was amplified, fragmented and hybridised to Illumina Infinium Human Methylation450 Beadchip using standard Illumina protocol
702
+ </Hybridization-Protocol>
703
+ <Scan-Protocol>
704
+ Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting
705
+ </Scan-Protocol>
706
+ <Description>
707
+ CFS Genomic DNA
708
+ </Description>
709
+ <Data-Processing>
710
+ BeadStudio software v3.2
711
+ </Data-Processing>
712
+ <Platform-Ref ref="GPL13534" />
713
+ <Contact-Ref ref="contrib1" />
714
+ <Supplementary-Data type="IDAT">
715
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739728/suppl/GSM2739728_3999356082_R02C01_Grn.idat.gz
716
+ </Supplementary-Data>
717
+ <Supplementary-Data type="IDAT">
718
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739728/suppl/GSM2739728_3999356082_R02C01_Red.idat.gz
719
+ </Supplementary-Data>
720
+ <Data-Table>
721
+ <Column position="1">
722
+ <Name>ID_REF</Name>
723
+ </Column>
724
+ <Column position="2">
725
+ <Name>VALUE</Name>
726
+ <Description>Average Beta non-normalized Beta</Description>
727
+ </Column>
728
+ <Column position="3">
729
+ <Name>Detection Pval</Name>
730
+ </Column>
731
+ <External-Data rows="467971">
732
+ GSM2739728-tbl-1.txt
733
+ </External-Data>
734
+ </Data-Table>
735
+ </Sample>
736
+
737
+ <Sample iid="GSM2739729">
738
+ <Status database="GEO">
739
+ <Submission-Date>2017-08-10</Submission-Date>
740
+ <Release-Date>2017-12-31</Release-Date>
741
+ <Last-Update-Date>2018-01-23</Last-Update-Date>
742
+ </Status>
743
+ <Title>PBMC Genomic DNA G00106</Title>
744
+ <Accession database="GEO">GSM2739729</Accession>
745
+ <Type>genomic</Type>
746
+ <Channel-Count>1</Channel-Count>
747
+ <Channel position="1">
748
+ <Source>PBMC</Source>
749
+ <Organism taxid="9606">Homo sapiens</Organism>
750
+ <Characteristics tag="Sex">
751
+ female
752
+ </Characteristics>
753
+ <Characteristics tag="disease state">
754
+ CFS
755
+ </Characteristics>
756
+ <Molecule>genomic DNA</Molecule>
757
+ <Extract-Protocol>
758
+ Genomic DNA was extracted and purified from Omega EZNA Tissue DNA Kit according to manufacturer's instructions
759
+ </Extract-Protocol>
760
+ <Label>Cy3 and Cy5</Label>
761
+ <Label-Protocol>
762
+ Standard Illumina Protocol
763
+ </Label-Protocol>
764
+ </Channel>
765
+ <Hybridization-Protocol>
766
+ Bisulfite converted DNA was amplified, fragmented and hybridised to Illumina Infinium Human Methylation450 Beadchip using standard Illumina protocol
767
+ </Hybridization-Protocol>
768
+ <Scan-Protocol>
769
+ Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting
770
+ </Scan-Protocol>
771
+ <Description>
772
+ CFS Genomic DNA
773
+ </Description>
774
+ <Data-Processing>
775
+ BeadStudio software v3.2
776
+ </Data-Processing>
777
+ <Platform-Ref ref="GPL13534" />
778
+ <Contact-Ref ref="contrib1" />
779
+ <Supplementary-Data type="IDAT">
780
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739729/suppl/GSM2739729_3999356082_R03C01_Grn.idat.gz
781
+ </Supplementary-Data>
782
+ <Supplementary-Data type="IDAT">
783
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739729/suppl/GSM2739729_3999356082_R03C01_Red.idat.gz
784
+ </Supplementary-Data>
785
+ <Data-Table>
786
+ <Column position="1">
787
+ <Name>ID_REF</Name>
788
+ </Column>
789
+ <Column position="2">
790
+ <Name>VALUE</Name>
791
+ <Description>Average Beta non-normalized Beta</Description>
792
+ </Column>
793
+ <Column position="3">
794
+ <Name>Detection Pval</Name>
795
+ </Column>
796
+ <External-Data rows="467971">
797
+ GSM2739729-tbl-1.txt
798
+ </External-Data>
799
+ </Data-Table>
800
+ </Sample>
801
+
802
+ <Sample iid="GSM2739730">
803
+ <Status database="GEO">
804
+ <Submission-Date>2017-08-10</Submission-Date>
805
+ <Release-Date>2017-12-31</Release-Date>
806
+ <Last-Update-Date>2018-01-23</Last-Update-Date>
807
+ </Status>
808
+ <Title>PBMC Genomic DNA G00111</Title>
809
+ <Accession database="GEO">GSM2739730</Accession>
810
+ <Type>genomic</Type>
811
+ <Channel-Count>1</Channel-Count>
812
+ <Channel position="1">
813
+ <Source>PBMC</Source>
814
+ <Organism taxid="9606">Homo sapiens</Organism>
815
+ <Characteristics tag="Sex">
816
+ female
817
+ </Characteristics>
818
+ <Characteristics tag="disease state">
819
+ CFS
820
+ </Characteristics>
821
+ <Molecule>genomic DNA</Molecule>
822
+ <Extract-Protocol>
823
+ Genomic DNA was extracted and purified from Omega EZNA Tissue DNA Kit according to manufacturer's instructions
824
+ </Extract-Protocol>
825
+ <Label>Cy3 and Cy5</Label>
826
+ <Label-Protocol>
827
+ Standard Illumina Protocol
828
+ </Label-Protocol>
829
+ </Channel>
830
+ <Hybridization-Protocol>
831
+ Bisulfite converted DNA was amplified, fragmented and hybridised to Illumina Infinium Human Methylation450 Beadchip using standard Illumina protocol
832
+ </Hybridization-Protocol>
833
+ <Scan-Protocol>
834
+ Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting
835
+ </Scan-Protocol>
836
+ <Description>
837
+ CFS Genomic DNA
838
+ </Description>
839
+ <Data-Processing>
840
+ BeadStudio software v3.2
841
+ </Data-Processing>
842
+ <Platform-Ref ref="GPL13534" />
843
+ <Contact-Ref ref="contrib1" />
844
+ <Supplementary-Data type="IDAT">
845
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739730/suppl/GSM2739730_3999356082_R04C01_Grn.idat.gz
846
+ </Supplementary-Data>
847
+ <Supplementary-Data type="IDAT">
848
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739730/suppl/GSM2739730_3999356082_R04C01_Red.idat.gz
849
+ </Supplementary-Data>
850
+ <Data-Table>
851
+ <Column position="1">
852
+ <Name>ID_REF</Name>
853
+ </Column>
854
+ <Column position="2">
855
+ <Name>VALUE</Name>
856
+ <Description>Average Beta non-normalized Beta</Description>
857
+ </Column>
858
+ <Column position="3">
859
+ <Name>Detection Pval</Name>
860
+ </Column>
861
+ <External-Data rows="467971">
862
+ GSM2739730-tbl-1.txt
863
+ </External-Data>
864
+ </Data-Table>
865
+ </Sample>
866
+
867
+ <Sample iid="GSM2739731">
868
+ <Status database="GEO">
869
+ <Submission-Date>2017-08-10</Submission-Date>
870
+ <Release-Date>2017-12-31</Release-Date>
871
+ <Last-Update-Date>2018-01-23</Last-Update-Date>
872
+ </Status>
873
+ <Title>PBMC Genomic DNA G00115</Title>
874
+ <Accession database="GEO">GSM2739731</Accession>
875
+ <Type>genomic</Type>
876
+ <Channel-Count>1</Channel-Count>
877
+ <Channel position="1">
878
+ <Source>PBMC</Source>
879
+ <Organism taxid="9606">Homo sapiens</Organism>
880
+ <Characteristics tag="Sex">
881
+ female
882
+ </Characteristics>
883
+ <Characteristics tag="disease state">
884
+ CFS
885
+ </Characteristics>
886
+ <Molecule>genomic DNA</Molecule>
887
+ <Extract-Protocol>
888
+ Genomic DNA was extracted and purified from Omega EZNA Tissue DNA Kit according to manufacturer's instructions
889
+ </Extract-Protocol>
890
+ <Label>Cy3 and Cy5</Label>
891
+ <Label-Protocol>
892
+ Standard Illumina Protocol
893
+ </Label-Protocol>
894
+ </Channel>
895
+ <Hybridization-Protocol>
896
+ Bisulfite converted DNA was amplified, fragmented and hybridised to Illumina Infinium Human Methylation450 Beadchip using standard Illumina protocol
897
+ </Hybridization-Protocol>
898
+ <Scan-Protocol>
899
+ Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting
900
+ </Scan-Protocol>
901
+ <Description>
902
+ CFS Genomic DNA
903
+ </Description>
904
+ <Data-Processing>
905
+ BeadStudio software v3.2
906
+ </Data-Processing>
907
+ <Platform-Ref ref="GPL13534" />
908
+ <Contact-Ref ref="contrib1" />
909
+ <Supplementary-Data type="IDAT">
910
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739731/suppl/GSM2739731_3999356082_R05C01_Grn.idat.gz
911
+ </Supplementary-Data>
912
+ <Supplementary-Data type="IDAT">
913
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739731/suppl/GSM2739731_3999356082_R05C01_Red.idat.gz
914
+ </Supplementary-Data>
915
+ <Data-Table>
916
+ <Column position="1">
917
+ <Name>ID_REF</Name>
918
+ </Column>
919
+ <Column position="2">
920
+ <Name>VALUE</Name>
921
+ <Description>Average Beta non-normalized Beta</Description>
922
+ </Column>
923
+ <Column position="3">
924
+ <Name>Detection Pval</Name>
925
+ </Column>
926
+ <External-Data rows="467971">
927
+ GSM2739731-tbl-1.txt
928
+ </External-Data>
929
+ </Data-Table>
930
+ </Sample>
931
+
932
+ <Sample iid="GSM2739732">
933
+ <Status database="GEO">
934
+ <Submission-Date>2017-08-10</Submission-Date>
935
+ <Release-Date>2017-12-31</Release-Date>
936
+ <Last-Update-Date>2018-01-23</Last-Update-Date>
937
+ </Status>
938
+ <Title>PBMC Genomic DNA G00124</Title>
939
+ <Accession database="GEO">GSM2739732</Accession>
940
+ <Type>genomic</Type>
941
+ <Channel-Count>1</Channel-Count>
942
+ <Channel position="1">
943
+ <Source>PBMC</Source>
944
+ <Organism taxid="9606">Homo sapiens</Organism>
945
+ <Characteristics tag="Sex">
946
+ female
947
+ </Characteristics>
948
+ <Characteristics tag="disease state">
949
+ CFS
950
+ </Characteristics>
951
+ <Molecule>genomic DNA</Molecule>
952
+ <Extract-Protocol>
953
+ Genomic DNA was extracted and purified from Omega EZNA Tissue DNA Kit according to manufacturer's instructions
954
+ </Extract-Protocol>
955
+ <Label>Cy3 and Cy5</Label>
956
+ <Label-Protocol>
957
+ Standard Illumina Protocol
958
+ </Label-Protocol>
959
+ </Channel>
960
+ <Hybridization-Protocol>
961
+ Bisulfite converted DNA was amplified, fragmented and hybridised to Illumina Infinium Human Methylation450 Beadchip using standard Illumina protocol
962
+ </Hybridization-Protocol>
963
+ <Scan-Protocol>
964
+ Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting
965
+ </Scan-Protocol>
966
+ <Description>
967
+ CFS Genomic DNA
968
+ </Description>
969
+ <Data-Processing>
970
+ BeadStudio software v3.2
971
+ </Data-Processing>
972
+ <Platform-Ref ref="GPL13534" />
973
+ <Contact-Ref ref="contrib1" />
974
+ <Supplementary-Data type="IDAT">
975
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739732/suppl/GSM2739732_3999356064_R01C01_Grn.idat.gz
976
+ </Supplementary-Data>
977
+ <Supplementary-Data type="IDAT">
978
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739732/suppl/GSM2739732_3999356064_R01C01_Red.idat.gz
979
+ </Supplementary-Data>
980
+ <Data-Table>
981
+ <Column position="1">
982
+ <Name>ID_REF</Name>
983
+ </Column>
984
+ <Column position="2">
985
+ <Name>VALUE</Name>
986
+ <Description>Average Beta non-normalized Beta</Description>
987
+ </Column>
988
+ <Column position="3">
989
+ <Name>Detection Pval</Name>
990
+ </Column>
991
+ <External-Data rows="467971">
992
+ GSM2739732-tbl-1.txt
993
+ </External-Data>
994
+ </Data-Table>
995
+ </Sample>
996
+
997
+ <Sample iid="GSM2739733">
998
+ <Status database="GEO">
999
+ <Submission-Date>2017-08-10</Submission-Date>
1000
+ <Release-Date>2017-12-31</Release-Date>
1001
+ <Last-Update-Date>2018-01-23</Last-Update-Date>
1002
+ </Status>
1003
+ <Title>PBMC Genomic DNA G00147</Title>
1004
+ <Accession database="GEO">GSM2739733</Accession>
1005
+ <Type>genomic</Type>
1006
+ <Channel-Count>1</Channel-Count>
1007
+ <Channel position="1">
1008
+ <Source>PBMC</Source>
1009
+ <Organism taxid="9606">Homo sapiens</Organism>
1010
+ <Characteristics tag="Sex">
1011
+ female
1012
+ </Characteristics>
1013
+ <Characteristics tag="disease state">
1014
+ CFS
1015
+ </Characteristics>
1016
+ <Molecule>genomic DNA</Molecule>
1017
+ <Extract-Protocol>
1018
+ Genomic DNA was extracted and purified from Omega EZNA Tissue DNA Kit according to manufacturer's instructions
1019
+ </Extract-Protocol>
1020
+ <Label>Cy3 and Cy5</Label>
1021
+ <Label-Protocol>
1022
+ Standard Illumina Protocol
1023
+ </Label-Protocol>
1024
+ </Channel>
1025
+ <Hybridization-Protocol>
1026
+ Bisulfite converted DNA was amplified, fragmented and hybridised to Illumina Infinium Human Methylation450 Beadchip using standard Illumina protocol
1027
+ </Hybridization-Protocol>
1028
+ <Scan-Protocol>
1029
+ Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting
1030
+ </Scan-Protocol>
1031
+ <Description>
1032
+ CFS Genomic DNA
1033
+ </Description>
1034
+ <Data-Processing>
1035
+ BeadStudio software v3.2
1036
+ </Data-Processing>
1037
+ <Platform-Ref ref="GPL13534" />
1038
+ <Contact-Ref ref="contrib1" />
1039
+ <Supplementary-Data type="IDAT">
1040
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739733/suppl/GSM2739733_3999356064_R02C01_Grn.idat.gz
1041
+ </Supplementary-Data>
1042
+ <Supplementary-Data type="IDAT">
1043
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739733/suppl/GSM2739733_3999356064_R02C01_Red.idat.gz
1044
+ </Supplementary-Data>
1045
+ <Data-Table>
1046
+ <Column position="1">
1047
+ <Name>ID_REF</Name>
1048
+ </Column>
1049
+ <Column position="2">
1050
+ <Name>VALUE</Name>
1051
+ <Description>Average Beta non-normalized Beta</Description>
1052
+ </Column>
1053
+ <Column position="3">
1054
+ <Name>Detection Pval</Name>
1055
+ </Column>
1056
+ <External-Data rows="467971">
1057
+ GSM2739733-tbl-1.txt
1058
+ </External-Data>
1059
+ </Data-Table>
1060
+ </Sample>
1061
+
1062
+ <Sample iid="GSM2739734">
1063
+ <Status database="GEO">
1064
+ <Submission-Date>2017-08-10</Submission-Date>
1065
+ <Release-Date>2017-12-31</Release-Date>
1066
+ <Last-Update-Date>2018-01-23</Last-Update-Date>
1067
+ </Status>
1068
+ <Title>PBMC Genomic DNA G00151</Title>
1069
+ <Accession database="GEO">GSM2739734</Accession>
1070
+ <Type>genomic</Type>
1071
+ <Channel-Count>1</Channel-Count>
1072
+ <Channel position="1">
1073
+ <Source>PBMC</Source>
1074
+ <Organism taxid="9606">Homo sapiens</Organism>
1075
+ <Characteristics tag="Sex">
1076
+ female
1077
+ </Characteristics>
1078
+ <Characteristics tag="disease state">
1079
+ CFS
1080
+ </Characteristics>
1081
+ <Molecule>genomic DNA</Molecule>
1082
+ <Extract-Protocol>
1083
+ Genomic DNA was extracted and purified from Omega EZNA Tissue DNA Kit according to manufacturer's instructions
1084
+ </Extract-Protocol>
1085
+ <Label>Cy3 and Cy5</Label>
1086
+ <Label-Protocol>
1087
+ Standard Illumina Protocol
1088
+ </Label-Protocol>
1089
+ </Channel>
1090
+ <Hybridization-Protocol>
1091
+ Bisulfite converted DNA was amplified, fragmented and hybridised to Illumina Infinium Human Methylation450 Beadchip using standard Illumina protocol
1092
+ </Hybridization-Protocol>
1093
+ <Scan-Protocol>
1094
+ Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting
1095
+ </Scan-Protocol>
1096
+ <Description>
1097
+ CFS Genomic DNA
1098
+ </Description>
1099
+ <Data-Processing>
1100
+ BeadStudio software v3.2
1101
+ </Data-Processing>
1102
+ <Platform-Ref ref="GPL13534" />
1103
+ <Contact-Ref ref="contrib1" />
1104
+ <Supplementary-Data type="IDAT">
1105
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739734/suppl/GSM2739734_3999356064_R03C01_Grn.idat.gz
1106
+ </Supplementary-Data>
1107
+ <Supplementary-Data type="IDAT">
1108
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739734/suppl/GSM2739734_3999356064_R03C01_Red.idat.gz
1109
+ </Supplementary-Data>
1110
+ <Data-Table>
1111
+ <Column position="1">
1112
+ <Name>ID_REF</Name>
1113
+ </Column>
1114
+ <Column position="2">
1115
+ <Name>VALUE</Name>
1116
+ <Description>Average Beta non-normalized Beta</Description>
1117
+ </Column>
1118
+ <Column position="3">
1119
+ <Name>Detection Pval</Name>
1120
+ </Column>
1121
+ <External-Data rows="467971">
1122
+ GSM2739734-tbl-1.txt
1123
+ </External-Data>
1124
+ </Data-Table>
1125
+ </Sample>
1126
+
1127
+ <Sample iid="GSM2739735">
1128
+ <Status database="GEO">
1129
+ <Submission-Date>2017-08-10</Submission-Date>
1130
+ <Release-Date>2017-12-31</Release-Date>
1131
+ <Last-Update-Date>2018-01-23</Last-Update-Date>
1132
+ </Status>
1133
+ <Title>PBMC Genomic DNA G00159</Title>
1134
+ <Accession database="GEO">GSM2739735</Accession>
1135
+ <Type>genomic</Type>
1136
+ <Channel-Count>1</Channel-Count>
1137
+ <Channel position="1">
1138
+ <Source>PBMC</Source>
1139
+ <Organism taxid="9606">Homo sapiens</Organism>
1140
+ <Characteristics tag="Sex">
1141
+ female
1142
+ </Characteristics>
1143
+ <Characteristics tag="disease state">
1144
+ CFS
1145
+ </Characteristics>
1146
+ <Molecule>genomic DNA</Molecule>
1147
+ <Extract-Protocol>
1148
+ Genomic DNA was extracted and purified from Omega EZNA Tissue DNA Kit according to manufacturer's instructions
1149
+ </Extract-Protocol>
1150
+ <Label>Cy3 and Cy5</Label>
1151
+ <Label-Protocol>
1152
+ Standard Illumina Protocol
1153
+ </Label-Protocol>
1154
+ </Channel>
1155
+ <Hybridization-Protocol>
1156
+ Bisulfite converted DNA was amplified, fragmented and hybridised to Illumina Infinium Human Methylation450 Beadchip using standard Illumina protocol
1157
+ </Hybridization-Protocol>
1158
+ <Scan-Protocol>
1159
+ Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting
1160
+ </Scan-Protocol>
1161
+ <Description>
1162
+ CFS Genomic DNA
1163
+ </Description>
1164
+ <Data-Processing>
1165
+ BeadStudio software v3.2
1166
+ </Data-Processing>
1167
+ <Platform-Ref ref="GPL13534" />
1168
+ <Contact-Ref ref="contrib1" />
1169
+ <Supplementary-Data type="IDAT">
1170
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739735/suppl/GSM2739735_3999356064_R04C01_Grn.idat.gz
1171
+ </Supplementary-Data>
1172
+ <Supplementary-Data type="IDAT">
1173
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739735/suppl/GSM2739735_3999356064_R04C01_Red.idat.gz
1174
+ </Supplementary-Data>
1175
+ <Data-Table>
1176
+ <Column position="1">
1177
+ <Name>ID_REF</Name>
1178
+ </Column>
1179
+ <Column position="2">
1180
+ <Name>VALUE</Name>
1181
+ <Description>Average Beta non-normalized Beta</Description>
1182
+ </Column>
1183
+ <Column position="3">
1184
+ <Name>Detection Pval</Name>
1185
+ </Column>
1186
+ <External-Data rows="467971">
1187
+ GSM2739735-tbl-1.txt
1188
+ </External-Data>
1189
+ </Data-Table>
1190
+ </Sample>
1191
+
1192
+ <Sample iid="GSM2739736">
1193
+ <Status database="GEO">
1194
+ <Submission-Date>2017-08-10</Submission-Date>
1195
+ <Release-Date>2017-12-31</Release-Date>
1196
+ <Last-Update-Date>2018-01-23</Last-Update-Date>
1197
+ </Status>
1198
+ <Title>PBMC Genomic DNA G00166</Title>
1199
+ <Accession database="GEO">GSM2739736</Accession>
1200
+ <Type>genomic</Type>
1201
+ <Channel-Count>1</Channel-Count>
1202
+ <Channel position="1">
1203
+ <Source>PBMC</Source>
1204
+ <Organism taxid="9606">Homo sapiens</Organism>
1205
+ <Characteristics tag="Sex">
1206
+ female
1207
+ </Characteristics>
1208
+ <Characteristics tag="disease state">
1209
+ CFS
1210
+ </Characteristics>
1211
+ <Molecule>genomic DNA</Molecule>
1212
+ <Extract-Protocol>
1213
+ Genomic DNA was extracted and purified from Omega EZNA Tissue DNA Kit according to manufacturer's instructions
1214
+ </Extract-Protocol>
1215
+ <Label>Cy3 and Cy5</Label>
1216
+ <Label-Protocol>
1217
+ Standard Illumina Protocol
1218
+ </Label-Protocol>
1219
+ </Channel>
1220
+ <Hybridization-Protocol>
1221
+ Bisulfite converted DNA was amplified, fragmented and hybridised to Illumina Infinium Human Methylation450 Beadchip using standard Illumina protocol
1222
+ </Hybridization-Protocol>
1223
+ <Scan-Protocol>
1224
+ Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting
1225
+ </Scan-Protocol>
1226
+ <Description>
1227
+ CFS Genomic DNA
1228
+ </Description>
1229
+ <Data-Processing>
1230
+ BeadStudio software v3.2
1231
+ </Data-Processing>
1232
+ <Platform-Ref ref="GPL13534" />
1233
+ <Contact-Ref ref="contrib1" />
1234
+ <Supplementary-Data type="IDAT">
1235
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739736/suppl/GSM2739736_3999356064_R05C01_Grn.idat.gz
1236
+ </Supplementary-Data>
1237
+ <Supplementary-Data type="IDAT">
1238
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739736/suppl/GSM2739736_3999356064_R05C01_Red.idat.gz
1239
+ </Supplementary-Data>
1240
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1241
+ <Column position="1">
1242
+ <Name>ID_REF</Name>
1243
+ </Column>
1244
+ <Column position="2">
1245
+ <Name>VALUE</Name>
1246
+ <Description>Average Beta non-normalized Beta</Description>
1247
+ </Column>
1248
+ <Column position="3">
1249
+ <Name>Detection Pval</Name>
1250
+ </Column>
1251
+ <External-Data rows="467971">
1252
+ GSM2739736-tbl-1.txt
1253
+ </External-Data>
1254
+ </Data-Table>
1255
+ </Sample>
1256
+
1257
+ <Sample iid="GSM2739737">
1258
+ <Status database="GEO">
1259
+ <Submission-Date>2017-08-10</Submission-Date>
1260
+ <Release-Date>2017-12-31</Release-Date>
1261
+ <Last-Update-Date>2018-01-23</Last-Update-Date>
1262
+ </Status>
1263
+ <Title>PBMC Genomic DNA G00172</Title>
1264
+ <Accession database="GEO">GSM2739737</Accession>
1265
+ <Type>genomic</Type>
1266
+ <Channel-Count>1</Channel-Count>
1267
+ <Channel position="1">
1268
+ <Source>PBMC</Source>
1269
+ <Organism taxid="9606">Homo sapiens</Organism>
1270
+ <Characteristics tag="Sex">
1271
+ female
1272
+ </Characteristics>
1273
+ <Characteristics tag="disease state">
1274
+ CFS
1275
+ </Characteristics>
1276
+ <Molecule>genomic DNA</Molecule>
1277
+ <Extract-Protocol>
1278
+ Genomic DNA was extracted and purified from Omega EZNA Tissue DNA Kit according to manufacturer's instructions
1279
+ </Extract-Protocol>
1280
+ <Label>Cy3 and Cy5</Label>
1281
+ <Label-Protocol>
1282
+ Standard Illumina Protocol
1283
+ </Label-Protocol>
1284
+ </Channel>
1285
+ <Hybridization-Protocol>
1286
+ Bisulfite converted DNA was amplified, fragmented and hybridised to Illumina Infinium Human Methylation450 Beadchip using standard Illumina protocol
1287
+ </Hybridization-Protocol>
1288
+ <Scan-Protocol>
1289
+ Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting
1290
+ </Scan-Protocol>
1291
+ <Description>
1292
+ CFS Genomic DNA
1293
+ </Description>
1294
+ <Data-Processing>
1295
+ BeadStudio software v3.2
1296
+ </Data-Processing>
1297
+ <Platform-Ref ref="GPL13534" />
1298
+ <Contact-Ref ref="contrib1" />
1299
+ <Supplementary-Data type="IDAT">
1300
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739737/suppl/GSM2739737_3999356064_R06C01_Grn.idat.gz
1301
+ </Supplementary-Data>
1302
+ <Supplementary-Data type="IDAT">
1303
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739737/suppl/GSM2739737_3999356064_R06C01_Red.idat.gz
1304
+ </Supplementary-Data>
1305
+ <Data-Table>
1306
+ <Column position="1">
1307
+ <Name>ID_REF</Name>
1308
+ </Column>
1309
+ <Column position="2">
1310
+ <Name>VALUE</Name>
1311
+ <Description>Average Beta non-normalized Beta</Description>
1312
+ </Column>
1313
+ <Column position="3">
1314
+ <Name>Detection Pval</Name>
1315
+ </Column>
1316
+ <External-Data rows="467971">
1317
+ GSM2739737-tbl-1.txt
1318
+ </External-Data>
1319
+ </Data-Table>
1320
+ </Sample>
1321
+
1322
+ <Sample iid="GSM2739738">
1323
+ <Status database="GEO">
1324
+ <Submission-Date>2017-08-10</Submission-Date>
1325
+ <Release-Date>2017-12-31</Release-Date>
1326
+ <Last-Update-Date>2018-01-23</Last-Update-Date>
1327
+ </Status>
1328
+ <Title>PBMC Genomic DNA G00181</Title>
1329
+ <Accession database="GEO">GSM2739738</Accession>
1330
+ <Type>genomic</Type>
1331
+ <Channel-Count>1</Channel-Count>
1332
+ <Channel position="1">
1333
+ <Source>PBMC</Source>
1334
+ <Organism taxid="9606">Homo sapiens</Organism>
1335
+ <Characteristics tag="Sex">
1336
+ female
1337
+ </Characteristics>
1338
+ <Characteristics tag="disease state">
1339
+ CFS
1340
+ </Characteristics>
1341
+ <Molecule>genomic DNA</Molecule>
1342
+ <Extract-Protocol>
1343
+ Genomic DNA was extracted and purified from Omega EZNA Tissue DNA Kit according to manufacturer's instructions
1344
+ </Extract-Protocol>
1345
+ <Label>Cy3 and Cy5</Label>
1346
+ <Label-Protocol>
1347
+ Standard Illumina Protocol
1348
+ </Label-Protocol>
1349
+ </Channel>
1350
+ <Hybridization-Protocol>
1351
+ Bisulfite converted DNA was amplified, fragmented and hybridised to Illumina Infinium Human Methylation450 Beadchip using standard Illumina protocol
1352
+ </Hybridization-Protocol>
1353
+ <Scan-Protocol>
1354
+ Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting
1355
+ </Scan-Protocol>
1356
+ <Description>
1357
+ CFS Genomic DNA
1358
+ </Description>
1359
+ <Data-Processing>
1360
+ BeadStudio software v3.2
1361
+ </Data-Processing>
1362
+ <Platform-Ref ref="GPL13534" />
1363
+ <Contact-Ref ref="contrib1" />
1364
+ <Supplementary-Data type="IDAT">
1365
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739738/suppl/GSM2739738_3999356028_R01C01_Grn.idat.gz
1366
+ </Supplementary-Data>
1367
+ <Supplementary-Data type="IDAT">
1368
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739738/suppl/GSM2739738_3999356028_R01C01_Red.idat.gz
1369
+ </Supplementary-Data>
1370
+ <Data-Table>
1371
+ <Column position="1">
1372
+ <Name>ID_REF</Name>
1373
+ </Column>
1374
+ <Column position="2">
1375
+ <Name>VALUE</Name>
1376
+ <Description>Average Beta non-normalized Beta</Description>
1377
+ </Column>
1378
+ <Column position="3">
1379
+ <Name>Detection Pval</Name>
1380
+ </Column>
1381
+ <External-Data rows="467971">
1382
+ GSM2739738-tbl-1.txt
1383
+ </External-Data>
1384
+ </Data-Table>
1385
+ </Sample>
1386
+
1387
+ <Sample iid="GSM2739739">
1388
+ <Status database="GEO">
1389
+ <Submission-Date>2017-08-10</Submission-Date>
1390
+ <Release-Date>2017-12-31</Release-Date>
1391
+ <Last-Update-Date>2018-01-23</Last-Update-Date>
1392
+ </Status>
1393
+ <Title>PBMC Genomic DNA G00194</Title>
1394
+ <Accession database="GEO">GSM2739739</Accession>
1395
+ <Type>genomic</Type>
1396
+ <Channel-Count>1</Channel-Count>
1397
+ <Channel position="1">
1398
+ <Source>PBMC</Source>
1399
+ <Organism taxid="9606">Homo sapiens</Organism>
1400
+ <Characteristics tag="Sex">
1401
+ female
1402
+ </Characteristics>
1403
+ <Characteristics tag="disease state">
1404
+ CFS
1405
+ </Characteristics>
1406
+ <Molecule>genomic DNA</Molecule>
1407
+ <Extract-Protocol>
1408
+ Genomic DNA was extracted and purified from Omega EZNA Tissue DNA Kit according to manufacturer's instructions
1409
+ </Extract-Protocol>
1410
+ <Label>Cy3 and Cy5</Label>
1411
+ <Label-Protocol>
1412
+ Standard Illumina Protocol
1413
+ </Label-Protocol>
1414
+ </Channel>
1415
+ <Hybridization-Protocol>
1416
+ Bisulfite converted DNA was amplified, fragmented and hybridised to Illumina Infinium Human Methylation450 Beadchip using standard Illumina protocol
1417
+ </Hybridization-Protocol>
1418
+ <Scan-Protocol>
1419
+ Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting
1420
+ </Scan-Protocol>
1421
+ <Description>
1422
+ CFS Genomic DNA
1423
+ </Description>
1424
+ <Data-Processing>
1425
+ BeadStudio software v3.2
1426
+ </Data-Processing>
1427
+ <Platform-Ref ref="GPL13534" />
1428
+ <Contact-Ref ref="contrib1" />
1429
+ <Supplementary-Data type="IDAT">
1430
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739739/suppl/GSM2739739_3999356028_R02C01_Grn.idat.gz
1431
+ </Supplementary-Data>
1432
+ <Supplementary-Data type="IDAT">
1433
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739739/suppl/GSM2739739_3999356028_R02C01_Red.idat.gz
1434
+ </Supplementary-Data>
1435
+ <Data-Table>
1436
+ <Column position="1">
1437
+ <Name>ID_REF</Name>
1438
+ </Column>
1439
+ <Column position="2">
1440
+ <Name>VALUE</Name>
1441
+ <Description>Average Beta non-normalized Beta</Description>
1442
+ </Column>
1443
+ <Column position="3">
1444
+ <Name>Detection Pval</Name>
1445
+ </Column>
1446
+ <External-Data rows="467971">
1447
+ GSM2739739-tbl-1.txt
1448
+ </External-Data>
1449
+ </Data-Table>
1450
+ </Sample>
1451
+
1452
+ <Sample iid="GSM2739740">
1453
+ <Status database="GEO">
1454
+ <Submission-Date>2017-08-10</Submission-Date>
1455
+ <Release-Date>2017-12-31</Release-Date>
1456
+ <Last-Update-Date>2018-01-23</Last-Update-Date>
1457
+ </Status>
1458
+ <Title>PBMC Genomic DNA G00198</Title>
1459
+ <Accession database="GEO">GSM2739740</Accession>
1460
+ <Type>genomic</Type>
1461
+ <Channel-Count>1</Channel-Count>
1462
+ <Channel position="1">
1463
+ <Source>PBMC</Source>
1464
+ <Organism taxid="9606">Homo sapiens</Organism>
1465
+ <Characteristics tag="Sex">
1466
+ female
1467
+ </Characteristics>
1468
+ <Characteristics tag="disease state">
1469
+ CFS
1470
+ </Characteristics>
1471
+ <Molecule>genomic DNA</Molecule>
1472
+ <Extract-Protocol>
1473
+ Genomic DNA was extracted and purified from Omega EZNA Tissue DNA Kit according to manufacturer's instructions
1474
+ </Extract-Protocol>
1475
+ <Label>Cy3 and Cy5</Label>
1476
+ <Label-Protocol>
1477
+ Standard Illumina Protocol
1478
+ </Label-Protocol>
1479
+ </Channel>
1480
+ <Hybridization-Protocol>
1481
+ Bisulfite converted DNA was amplified, fragmented and hybridised to Illumina Infinium Human Methylation450 Beadchip using standard Illumina protocol
1482
+ </Hybridization-Protocol>
1483
+ <Scan-Protocol>
1484
+ Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting
1485
+ </Scan-Protocol>
1486
+ <Description>
1487
+ CFS Genomic DNA
1488
+ </Description>
1489
+ <Data-Processing>
1490
+ BeadStudio software v3.2
1491
+ </Data-Processing>
1492
+ <Platform-Ref ref="GPL13534" />
1493
+ <Contact-Ref ref="contrib1" />
1494
+ <Supplementary-Data type="IDAT">
1495
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739740/suppl/GSM2739740_3999356028_R03C01_Grn.idat.gz
1496
+ </Supplementary-Data>
1497
+ <Supplementary-Data type="IDAT">
1498
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739740/suppl/GSM2739740_3999356028_R03C01_Red.idat.gz
1499
+ </Supplementary-Data>
1500
+ <Data-Table>
1501
+ <Column position="1">
1502
+ <Name>ID_REF</Name>
1503
+ </Column>
1504
+ <Column position="2">
1505
+ <Name>VALUE</Name>
1506
+ <Description>Average Beta non-normalized Beta</Description>
1507
+ </Column>
1508
+ <Column position="3">
1509
+ <Name>Detection Pval</Name>
1510
+ </Column>
1511
+ <External-Data rows="467971">
1512
+ GSM2739740-tbl-1.txt
1513
+ </External-Data>
1514
+ </Data-Table>
1515
+ </Sample>
1516
+
1517
+ <Sample iid="GSM2739741">
1518
+ <Status database="GEO">
1519
+ <Submission-Date>2017-08-10</Submission-Date>
1520
+ <Release-Date>2017-12-31</Release-Date>
1521
+ <Last-Update-Date>2018-01-23</Last-Update-Date>
1522
+ </Status>
1523
+ <Title>PBMC Genomic DNA G00222</Title>
1524
+ <Accession database="GEO">GSM2739741</Accession>
1525
+ <Type>genomic</Type>
1526
+ <Channel-Count>1</Channel-Count>
1527
+ <Channel position="1">
1528
+ <Source>PBMC</Source>
1529
+ <Organism taxid="9606">Homo sapiens</Organism>
1530
+ <Characteristics tag="Sex">
1531
+ female
1532
+ </Characteristics>
1533
+ <Characteristics tag="disease state">
1534
+ CFS
1535
+ </Characteristics>
1536
+ <Molecule>genomic DNA</Molecule>
1537
+ <Extract-Protocol>
1538
+ Genomic DNA was extracted and purified from Omega EZNA Tissue DNA Kit according to manufacturer's instructions
1539
+ </Extract-Protocol>
1540
+ <Label>Cy3 and Cy5</Label>
1541
+ <Label-Protocol>
1542
+ Standard Illumina Protocol
1543
+ </Label-Protocol>
1544
+ </Channel>
1545
+ <Hybridization-Protocol>
1546
+ Bisulfite converted DNA was amplified, fragmented and hybridised to Illumina Infinium Human Methylation450 Beadchip using standard Illumina protocol
1547
+ </Hybridization-Protocol>
1548
+ <Scan-Protocol>
1549
+ Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting
1550
+ </Scan-Protocol>
1551
+ <Description>
1552
+ CFS Genomic DNA
1553
+ </Description>
1554
+ <Data-Processing>
1555
+ BeadStudio software v3.2
1556
+ </Data-Processing>
1557
+ <Platform-Ref ref="GPL13534" />
1558
+ <Contact-Ref ref="contrib1" />
1559
+ <Supplementary-Data type="IDAT">
1560
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739741/suppl/GSM2739741_3999356028_R04C01_Grn.idat.gz
1561
+ </Supplementary-Data>
1562
+ <Supplementary-Data type="IDAT">
1563
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739741/suppl/GSM2739741_3999356028_R04C01_Red.idat.gz
1564
+ </Supplementary-Data>
1565
+ <Data-Table>
1566
+ <Column position="1">
1567
+ <Name>ID_REF</Name>
1568
+ </Column>
1569
+ <Column position="2">
1570
+ <Name>VALUE</Name>
1571
+ <Description>Average Beta non-normalized Beta</Description>
1572
+ </Column>
1573
+ <Column position="3">
1574
+ <Name>Detection Pval</Name>
1575
+ </Column>
1576
+ <External-Data rows="467971">
1577
+ GSM2739741-tbl-1.txt
1578
+ </External-Data>
1579
+ </Data-Table>
1580
+ </Sample>
1581
+
1582
+ <Sample iid="GSM2739742">
1583
+ <Status database="GEO">
1584
+ <Submission-Date>2017-08-10</Submission-Date>
1585
+ <Release-Date>2017-12-31</Release-Date>
1586
+ <Last-Update-Date>2018-01-23</Last-Update-Date>
1587
+ </Status>
1588
+ <Title>PBMC Genomic DNA G00244</Title>
1589
+ <Accession database="GEO">GSM2739742</Accession>
1590
+ <Type>genomic</Type>
1591
+ <Channel-Count>1</Channel-Count>
1592
+ <Channel position="1">
1593
+ <Source>PBMC</Source>
1594
+ <Organism taxid="9606">Homo sapiens</Organism>
1595
+ <Characteristics tag="Sex">
1596
+ female
1597
+ </Characteristics>
1598
+ <Characteristics tag="disease state">
1599
+ CFS
1600
+ </Characteristics>
1601
+ <Molecule>genomic DNA</Molecule>
1602
+ <Extract-Protocol>
1603
+ Genomic DNA was extracted and purified from Omega EZNA Tissue DNA Kit according to manufacturer's instructions
1604
+ </Extract-Protocol>
1605
+ <Label>Cy3 and Cy5</Label>
1606
+ <Label-Protocol>
1607
+ Standard Illumina Protocol
1608
+ </Label-Protocol>
1609
+ </Channel>
1610
+ <Hybridization-Protocol>
1611
+ Bisulfite converted DNA was amplified, fragmented and hybridised to Illumina Infinium Human Methylation450 Beadchip using standard Illumina protocol
1612
+ </Hybridization-Protocol>
1613
+ <Scan-Protocol>
1614
+ Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting
1615
+ </Scan-Protocol>
1616
+ <Description>
1617
+ CFS Genomic DNA
1618
+ </Description>
1619
+ <Data-Processing>
1620
+ BeadStudio software v3.2
1621
+ </Data-Processing>
1622
+ <Platform-Ref ref="GPL13534" />
1623
+ <Contact-Ref ref="contrib1" />
1624
+ <Supplementary-Data type="IDAT">
1625
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739742/suppl/GSM2739742_3999356028_R05C01_Grn.idat.gz
1626
+ </Supplementary-Data>
1627
+ <Supplementary-Data type="IDAT">
1628
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739742/suppl/GSM2739742_3999356028_R05C01_Red.idat.gz
1629
+ </Supplementary-Data>
1630
+ <Data-Table>
1631
+ <Column position="1">
1632
+ <Name>ID_REF</Name>
1633
+ </Column>
1634
+ <Column position="2">
1635
+ <Name>VALUE</Name>
1636
+ <Description>Average Beta non-normalized Beta</Description>
1637
+ </Column>
1638
+ <Column position="3">
1639
+ <Name>Detection Pval</Name>
1640
+ </Column>
1641
+ <External-Data rows="467971">
1642
+ GSM2739742-tbl-1.txt
1643
+ </External-Data>
1644
+ </Data-Table>
1645
+ </Sample>
1646
+
1647
+ <Sample iid="GSM2739743">
1648
+ <Status database="GEO">
1649
+ <Submission-Date>2017-08-10</Submission-Date>
1650
+ <Release-Date>2017-12-31</Release-Date>
1651
+ <Last-Update-Date>2018-01-23</Last-Update-Date>
1652
+ </Status>
1653
+ <Title>PBMC Genomic DNA G00256</Title>
1654
+ <Accession database="GEO">GSM2739743</Accession>
1655
+ <Type>genomic</Type>
1656
+ <Channel-Count>1</Channel-Count>
1657
+ <Channel position="1">
1658
+ <Source>PBMC</Source>
1659
+ <Organism taxid="9606">Homo sapiens</Organism>
1660
+ <Characteristics tag="Sex">
1661
+ female
1662
+ </Characteristics>
1663
+ <Characteristics tag="disease state">
1664
+ CFS
1665
+ </Characteristics>
1666
+ <Molecule>genomic DNA</Molecule>
1667
+ <Extract-Protocol>
1668
+ Genomic DNA was extracted and purified from Omega EZNA Tissue DNA Kit according to manufacturer's instructions
1669
+ </Extract-Protocol>
1670
+ <Label>Cy3 and Cy5</Label>
1671
+ <Label-Protocol>
1672
+ Standard Illumina Protocol
1673
+ </Label-Protocol>
1674
+ </Channel>
1675
+ <Hybridization-Protocol>
1676
+ Bisulfite converted DNA was amplified, fragmented and hybridised to Illumina Infinium Human Methylation450 Beadchip using standard Illumina protocol
1677
+ </Hybridization-Protocol>
1678
+ <Scan-Protocol>
1679
+ Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting
1680
+ </Scan-Protocol>
1681
+ <Description>
1682
+ CFS Genomic DNA
1683
+ </Description>
1684
+ <Data-Processing>
1685
+ BeadStudio software v3.2
1686
+ </Data-Processing>
1687
+ <Platform-Ref ref="GPL13534" />
1688
+ <Contact-Ref ref="contrib1" />
1689
+ <Supplementary-Data type="IDAT">
1690
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739743/suppl/GSM2739743_3999356028_R06C01_Grn.idat.gz
1691
+ </Supplementary-Data>
1692
+ <Supplementary-Data type="IDAT">
1693
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739743/suppl/GSM2739743_3999356028_R06C01_Red.idat.gz
1694
+ </Supplementary-Data>
1695
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1696
+ <Column position="1">
1697
+ <Name>ID_REF</Name>
1698
+ </Column>
1699
+ <Column position="2">
1700
+ <Name>VALUE</Name>
1701
+ <Description>Average Beta non-normalized Beta</Description>
1702
+ </Column>
1703
+ <Column position="3">
1704
+ <Name>Detection Pval</Name>
1705
+ </Column>
1706
+ <External-Data rows="467971">
1707
+ GSM2739743-tbl-1.txt
1708
+ </External-Data>
1709
+ </Data-Table>
1710
+ </Sample>
1711
+
1712
+ <Sample iid="GSM2739744">
1713
+ <Status database="GEO">
1714
+ <Submission-Date>2017-08-10</Submission-Date>
1715
+ <Release-Date>2017-12-31</Release-Date>
1716
+ <Last-Update-Date>2018-01-23</Last-Update-Date>
1717
+ </Status>
1718
+ <Title>PBMC Genomic DNA G00262</Title>
1719
+ <Accession database="GEO">GSM2739744</Accession>
1720
+ <Type>genomic</Type>
1721
+ <Channel-Count>1</Channel-Count>
1722
+ <Channel position="1">
1723
+ <Source>PBMC</Source>
1724
+ <Organism taxid="9606">Homo sapiens</Organism>
1725
+ <Characteristics tag="Sex">
1726
+ female
1727
+ </Characteristics>
1728
+ <Characteristics tag="disease state">
1729
+ CFS
1730
+ </Characteristics>
1731
+ <Molecule>genomic DNA</Molecule>
1732
+ <Extract-Protocol>
1733
+ Genomic DNA was extracted and purified from Omega EZNA Tissue DNA Kit according to manufacturer's instructions
1734
+ </Extract-Protocol>
1735
+ <Label>Cy3 and Cy5</Label>
1736
+ <Label-Protocol>
1737
+ Standard Illumina Protocol
1738
+ </Label-Protocol>
1739
+ </Channel>
1740
+ <Hybridization-Protocol>
1741
+ Bisulfite converted DNA was amplified, fragmented and hybridised to Illumina Infinium Human Methylation450 Beadchip using standard Illumina protocol
1742
+ </Hybridization-Protocol>
1743
+ <Scan-Protocol>
1744
+ Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting
1745
+ </Scan-Protocol>
1746
+ <Description>
1747
+ CFS Genomic DNA
1748
+ </Description>
1749
+ <Data-Processing>
1750
+ BeadStudio software v3.2
1751
+ </Data-Processing>
1752
+ <Platform-Ref ref="GPL13534" />
1753
+ <Contact-Ref ref="contrib1" />
1754
+ <Supplementary-Data type="IDAT">
1755
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739744/suppl/GSM2739744_3999834039_R01C01_Grn.idat.gz
1756
+ </Supplementary-Data>
1757
+ <Supplementary-Data type="IDAT">
1758
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM2739nnn/GSM2739744/suppl/GSM2739744_3999834039_R01C01_Red.idat.gz
1759
+ </Supplementary-Data>
1760
+ <Data-Table>
1761
+ <Column position="1">
1762
+ <Name>ID_REF</Name>
1763
+ </Column>
1764
+ <Column position="2">
1765
+ <Name>VALUE</Name>
1766
+ <Description>Average Beta non-normalized Beta</Description>
1767
+ </Column>
1768
+ <Column position="3">
1769
+ <Name>Detection Pval</Name>
1770
+ </Column>
1771
+ <External-Data rows="467971">
1772
+ GSM2739744-tbl-1.txt
1773
+ </External-Data>
1774
+ </Data-Table>
1775
+ </Sample>
1776
+
1777
+ <Sample iid="GSM2739745">
1778
+ <Status database="GEO">
1779
+ <Submission-Date>2017-08-10</Submission-Date>
1780
+ <Release-Date>2017-12-31</Release-Date>
1781
+ <Last-Update-Date>2018-01-23</Last-Update-Date>
1782
+ </Status>
1783
+ <Title>PBMC Genomic DNA G00263</Title>
1784
+ <Accession database="GEO">GSM2739745</Accession>
1785
+ <Type>genomic</Type>
1786
+ <Channel-Count>1</Channel-Count>
1787
+ <Channel position="1">
1788
+ <Source>PBMC</Source>
1789
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+ <Type>genomic</Type>
289
+ <Channel-Count>1</Channel-Count>
290
+ <Channel position="1">
291
+ <Source>ME/CFS PBMC</Source>
292
+ <Organism taxid="9606">Homo sapiens</Organism>
293
+ <Characteristics tag="gender">
294
+ female
295
+ </Characteristics>
296
+ <Characteristics tag="subject id">
297
+ ME/CFS subject 2
298
+ </Characteristics>
299
+ <Characteristics tag="disease state">
300
+ Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS)
301
+ </Characteristics>
302
+ <Characteristics tag="cell type">
303
+ peripheral blood mononuclear cells (PBMC)
304
+ </Characteristics>
305
+ <Molecule>genomic DNA</Molecule>
306
+ <Extract-Protocol>
307
+ genomic DNA was extracted and purified from PBMC samples using Qiagen DNeasy Blood &amp; Tissue Kit according to manufacturer instructions
308
+ </Extract-Protocol>
309
+ <Label>Cy3, Cy5</Label>
310
+ <Label-Protocol>
311
+ Standard Illumina Protocol
312
+ </Label-Protocol>
313
+ </Channel>
314
+ <Hybridization-Protocol>
315
+ bisulphite converted DNA was hybridised to Illumina Infinium MethylationEPIC Beadchip using standard Illumina protocol
316
+ </Hybridization-Protocol>
317
+ <Scan-Protocol>
318
+ Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting
319
+ </Scan-Protocol>
320
+ <Description>
321
+ PBMC genomic DNA from ME/CFS subject 2
322
+ </Description>
323
+ <Data-Processing>
324
+ Illumina Genome Studio; Matrix signal intensities contains unmethylated and methylated signal intensities; Matrix processed contains non-normalized average beta values.
325
+ </Data-Processing>
326
+ <Platform-Ref ref="GPL21145" />
327
+ <Contact-Ref ref="contrib1" />
328
+ <Supplementary-Data type="unknown">
329
+ NONE
330
+ </Supplementary-Data>
331
+ <Data-Table>
332
+ <Column position="1">
333
+ <Name>ID_REF</Name>
334
+ </Column>
335
+ <Column position="2">
336
+ <Name>VALUE</Name>
337
+ <Description>Average Beta</Description>
338
+ </Column>
339
+ <Column position="3">
340
+ <Name>Detection Pval</Name>
341
+ </Column>
342
+ <External-Data rows="866895">
343
+ GSM3024929-tbl-1.txt
344
+ </External-Data>
345
+ </Data-Table>
346
+ </Sample>
347
+
348
+ <Sample iid="GSM3024930">
349
+ <Status database="GEO">
350
+ <Submission-Date>2018-02-27</Submission-Date>
351
+ <Release-Date>2018-07-23</Release-Date>
352
+ <Last-Update-Date>2018-07-23</Last-Update-Date>
353
+ </Status>
354
+ <Title>PBMC genomic DNA ME/CFS 3</Title>
355
+ <Accession database="GEO">GSM3024930</Accession>
356
+ <Type>genomic</Type>
357
+ <Channel-Count>1</Channel-Count>
358
+ <Channel position="1">
359
+ <Source>ME/CFS PBMC</Source>
360
+ <Organism taxid="9606">Homo sapiens</Organism>
361
+ <Characteristics tag="gender">
362
+ female
363
+ </Characteristics>
364
+ <Characteristics tag="subject id">
365
+ ME/CFS subject 3
366
+ </Characteristics>
367
+ <Characteristics tag="disease state">
368
+ Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS)
369
+ </Characteristics>
370
+ <Characteristics tag="cell type">
371
+ peripheral blood mononuclear cells (PBMC)
372
+ </Characteristics>
373
+ <Molecule>genomic DNA</Molecule>
374
+ <Extract-Protocol>
375
+ genomic DNA was extracted and purified from PBMC samples using Qiagen DNeasy Blood &amp; Tissue Kit according to manufacturer instructions
376
+ </Extract-Protocol>
377
+ <Label>Cy3, Cy5</Label>
378
+ <Label-Protocol>
379
+ Standard Illumina Protocol
380
+ </Label-Protocol>
381
+ </Channel>
382
+ <Hybridization-Protocol>
383
+ bisulphite converted DNA was hybridised to Illumina Infinium MethylationEPIC Beadchip using standard Illumina protocol
384
+ </Hybridization-Protocol>
385
+ <Scan-Protocol>
386
+ Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting
387
+ </Scan-Protocol>
388
+ <Description>
389
+ PBMC genomic DNA from ME/CFS subject 3
390
+ </Description>
391
+ <Data-Processing>
392
+ Illumina Genome Studio; Matrix signal intensities contains unmethylated and methylated signal intensities; Matrix processed contains non-normalized average beta values.
393
+ </Data-Processing>
394
+ <Platform-Ref ref="GPL21145" />
395
+ <Contact-Ref ref="contrib1" />
396
+ <Supplementary-Data type="unknown">
397
+ NONE
398
+ </Supplementary-Data>
399
+ <Data-Table>
400
+ <Column position="1">
401
+ <Name>ID_REF</Name>
402
+ </Column>
403
+ <Column position="2">
404
+ <Name>VALUE</Name>
405
+ <Description>Average Beta</Description>
406
+ </Column>
407
+ <Column position="3">
408
+ <Name>Detection Pval</Name>
409
+ </Column>
410
+ <External-Data rows="866895">
411
+ GSM3024930-tbl-1.txt
412
+ </External-Data>
413
+ </Data-Table>
414
+ </Sample>
415
+
416
+ <Sample iid="GSM3024931">
417
+ <Status database="GEO">
418
+ <Submission-Date>2018-02-27</Submission-Date>
419
+ <Release-Date>2018-07-23</Release-Date>
420
+ <Last-Update-Date>2018-07-23</Last-Update-Date>
421
+ </Status>
422
+ <Title>PBMC genomic DNA Healthy Control (HC) 2</Title>
423
+ <Accession database="GEO">GSM3024931</Accession>
424
+ <Type>genomic</Type>
425
+ <Channel-Count>1</Channel-Count>
426
+ <Channel position="1">
427
+ <Source>HC PBMC</Source>
428
+ <Organism taxid="9606">Homo sapiens</Organism>
429
+ <Characteristics tag="gender">
430
+ female
431
+ </Characteristics>
432
+ <Characteristics tag="subject id">
433
+ HC subject 2
434
+ </Characteristics>
435
+ <Characteristics tag="disease state">
436
+ Healthy Control (HC)
437
+ </Characteristics>
438
+ <Characteristics tag="cell type">
439
+ peripheral blood mononuclear cells (PBMC)
440
+ </Characteristics>
441
+ <Molecule>genomic DNA</Molecule>
442
+ <Extract-Protocol>
443
+ genomic DNA was extracted and purified from PBMC samples using Qiagen DNeasy Blood &amp; Tissue Kit according to manufacturer instructions
444
+ </Extract-Protocol>
445
+ <Label>Cy3, Cy5</Label>
446
+ <Label-Protocol>
447
+ Standard Illumina Protocol
448
+ </Label-Protocol>
449
+ </Channel>
450
+ <Hybridization-Protocol>
451
+ bisulphite converted DNA was hybridised to Illumina Infinium MethylationEPIC Beadchip using standard Illumina protocol
452
+ </Hybridization-Protocol>
453
+ <Scan-Protocol>
454
+ Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting
455
+ </Scan-Protocol>
456
+ <Description>
457
+ PBMC genomic DNA from HC subject 2
458
+ </Description>
459
+ <Data-Processing>
460
+ Illumina Genome Studio; Matrix signal intensities contains unmethylated and methylated signal intensities; Matrix processed contains non-normalized average beta values.
461
+ </Data-Processing>
462
+ <Platform-Ref ref="GPL21145" />
463
+ <Contact-Ref ref="contrib1" />
464
+ <Supplementary-Data type="unknown">
465
+ NONE
466
+ </Supplementary-Data>
467
+ <Data-Table>
468
+ <Column position="1">
469
+ <Name>ID_REF</Name>
470
+ </Column>
471
+ <Column position="2">
472
+ <Name>VALUE</Name>
473
+ <Description>Average Beta</Description>
474
+ </Column>
475
+ <Column position="3">
476
+ <Name>Detection Pval</Name>
477
+ </Column>
478
+ <External-Data rows="866895">
479
+ GSM3024931-tbl-1.txt
480
+ </External-Data>
481
+ </Data-Table>
482
+ </Sample>
483
+
484
+ <Sample iid="GSM3024932">
485
+ <Status database="GEO">
486
+ <Submission-Date>2018-02-27</Submission-Date>
487
+ <Release-Date>2018-07-23</Release-Date>
488
+ <Last-Update-Date>2018-07-23</Last-Update-Date>
489
+ </Status>
490
+ <Title>PBMC genomic DNA Healthy Control (HC) 3</Title>
491
+ <Accession database="GEO">GSM3024932</Accession>
492
+ <Type>genomic</Type>
493
+ <Channel-Count>1</Channel-Count>
494
+ <Channel position="1">
495
+ <Source>HC PBMC</Source>
496
+ <Organism taxid="9606">Homo sapiens</Organism>
497
+ <Characteristics tag="gender">
498
+ female
499
+ </Characteristics>
500
+ <Characteristics tag="subject id">
501
+ HC subject 3
502
+ </Characteristics>
503
+ <Characteristics tag="disease state">
504
+ Healthy Control (HC)
505
+ </Characteristics>
506
+ <Characteristics tag="cell type">
507
+ peripheral blood mononuclear cells (PBMC)
508
+ </Characteristics>
509
+ <Molecule>genomic DNA</Molecule>
510
+ <Extract-Protocol>
511
+ genomic DNA was extracted and purified from PBMC samples using Qiagen DNeasy Blood &amp; Tissue Kit according to manufacturer instructions
512
+ </Extract-Protocol>
513
+ <Label>Cy3, Cy5</Label>
514
+ <Label-Protocol>
515
+ Standard Illumina Protocol
516
+ </Label-Protocol>
517
+ </Channel>
518
+ <Hybridization-Protocol>
519
+ bisulphite converted DNA was hybridised to Illumina Infinium MethylationEPIC Beadchip using standard Illumina protocol
520
+ </Hybridization-Protocol>
521
+ <Scan-Protocol>
522
+ Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting
523
+ </Scan-Protocol>
524
+ <Description>
525
+ PBMC genomic DNA from HC subject 3
526
+ </Description>
527
+ <Data-Processing>
528
+ Illumina Genome Studio; Matrix signal intensities contains unmethylated and methylated signal intensities; Matrix processed contains non-normalized average beta values.
529
+ </Data-Processing>
530
+ <Platform-Ref ref="GPL21145" />
531
+ <Contact-Ref ref="contrib1" />
532
+ <Supplementary-Data type="unknown">
533
+ NONE
534
+ </Supplementary-Data>
535
+ <Data-Table>
536
+ <Column position="1">
537
+ <Name>ID_REF</Name>
538
+ </Column>
539
+ <Column position="2">
540
+ <Name>VALUE</Name>
541
+ <Description>Average Beta</Description>
542
+ </Column>
543
+ <Column position="3">
544
+ <Name>Detection Pval</Name>
545
+ </Column>
546
+ <External-Data rows="866895">
547
+ GSM3024932-tbl-1.txt
548
+ </External-Data>
549
+ </Data-Table>
550
+ </Sample>
551
+
552
+ <Sample iid="GSM3024933">
553
+ <Status database="GEO">
554
+ <Submission-Date>2018-02-27</Submission-Date>
555
+ <Release-Date>2018-07-23</Release-Date>
556
+ <Last-Update-Date>2018-07-23</Last-Update-Date>
557
+ </Status>
558
+ <Title>PBMC genomic DNA ME/CFS 4</Title>
559
+ <Accession database="GEO">GSM3024933</Accession>
560
+ <Type>genomic</Type>
561
+ <Channel-Count>1</Channel-Count>
562
+ <Channel position="1">
563
+ <Source>ME/CFS PBMC</Source>
564
+ <Organism taxid="9606">Homo sapiens</Organism>
565
+ <Characteristics tag="gender">
566
+ female
567
+ </Characteristics>
568
+ <Characteristics tag="subject id">
569
+ ME/CFS subject 4
570
+ </Characteristics>
571
+ <Characteristics tag="disease state">
572
+ Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS)
573
+ </Characteristics>
574
+ <Characteristics tag="cell type">
575
+ peripheral blood mononuclear cells (PBMC)
576
+ </Characteristics>
577
+ <Molecule>genomic DNA</Molecule>
578
+ <Extract-Protocol>
579
+ genomic DNA was extracted and purified from PBMC samples using Qiagen DNeasy Blood &amp; Tissue Kit according to manufacturer instructions
580
+ </Extract-Protocol>
581
+ <Label>Cy3, Cy5</Label>
582
+ <Label-Protocol>
583
+ Standard Illumina Protocol
584
+ </Label-Protocol>
585
+ </Channel>
586
+ <Hybridization-Protocol>
587
+ bisulphite converted DNA was hybridised to Illumina Infinium MethylationEPIC Beadchip using standard Illumina protocol
588
+ </Hybridization-Protocol>
589
+ <Scan-Protocol>
590
+ Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting
591
+ </Scan-Protocol>
592
+ <Description>
593
+ PBMC genomic DNA from ME/CFS subject 4
594
+ </Description>
595
+ <Data-Processing>
596
+ Illumina Genome Studio; Matrix signal intensities contains unmethylated and methylated signal intensities; Matrix processed contains non-normalized average beta values.
597
+ </Data-Processing>
598
+ <Platform-Ref ref="GPL21145" />
599
+ <Contact-Ref ref="contrib1" />
600
+ <Supplementary-Data type="unknown">
601
+ NONE
602
+ </Supplementary-Data>
603
+ <Data-Table>
604
+ <Column position="1">
605
+ <Name>ID_REF</Name>
606
+ </Column>
607
+ <Column position="2">
608
+ <Name>VALUE</Name>
609
+ <Description>Average Beta</Description>
610
+ </Column>
611
+ <Column position="3">
612
+ <Name>Detection Pval</Name>
613
+ </Column>
614
+ <External-Data rows="866895">
615
+ GSM3024933-tbl-1.txt
616
+ </External-Data>
617
+ </Data-Table>
618
+ </Sample>
619
+
620
+ <Sample iid="GSM3024934">
621
+ <Status database="GEO">
622
+ <Submission-Date>2018-02-27</Submission-Date>
623
+ <Release-Date>2018-07-23</Release-Date>
624
+ <Last-Update-Date>2018-07-23</Last-Update-Date>
625
+ </Status>
626
+ <Title>PBMC genomic DNA ME/CFS 5</Title>
627
+ <Accession database="GEO">GSM3024934</Accession>
628
+ <Type>genomic</Type>
629
+ <Channel-Count>1</Channel-Count>
630
+ <Channel position="1">
631
+ <Source>ME/CFS PBMC</Source>
632
+ <Organism taxid="9606">Homo sapiens</Organism>
633
+ <Characteristics tag="gender">
634
+ female
635
+ </Characteristics>
636
+ <Characteristics tag="subject id">
637
+ ME/CFS subject 5
638
+ </Characteristics>
639
+ <Characteristics tag="disease state">
640
+ Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS)
641
+ </Characteristics>
642
+ <Characteristics tag="cell type">
643
+ peripheral blood mononuclear cells (PBMC)
644
+ </Characteristics>
645
+ <Molecule>genomic DNA</Molecule>
646
+ <Extract-Protocol>
647
+ genomic DNA was extracted and purified from PBMC samples using Qiagen DNeasy Blood &amp; Tissue Kit according to manufacturer instructions
648
+ </Extract-Protocol>
649
+ <Label>Cy3, Cy5</Label>
650
+ <Label-Protocol>
651
+ Standard Illumina Protocol
652
+ </Label-Protocol>
653
+ </Channel>
654
+ <Hybridization-Protocol>
655
+ bisulphite converted DNA was hybridised to Illumina Infinium MethylationEPIC Beadchip using standard Illumina protocol
656
+ </Hybridization-Protocol>
657
+ <Scan-Protocol>
658
+ Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting
659
+ </Scan-Protocol>
660
+ <Description>
661
+ PBMC genomic DNA from ME/CFS subject 5
662
+ </Description>
663
+ <Data-Processing>
664
+ Illumina Genome Studio; Matrix signal intensities contains unmethylated and methylated signal intensities; Matrix processed contains non-normalized average beta values.
665
+ </Data-Processing>
666
+ <Platform-Ref ref="GPL21145" />
667
+ <Contact-Ref ref="contrib1" />
668
+ <Supplementary-Data type="unknown">
669
+ NONE
670
+ </Supplementary-Data>
671
+ <Data-Table>
672
+ <Column position="1">
673
+ <Name>ID_REF</Name>
674
+ </Column>
675
+ <Column position="2">
676
+ <Name>VALUE</Name>
677
+ <Description>Average Beta</Description>
678
+ </Column>
679
+ <Column position="3">
680
+ <Name>Detection Pval</Name>
681
+ </Column>
682
+ <External-Data rows="866895">
683
+ GSM3024934-tbl-1.txt
684
+ </External-Data>
685
+ </Data-Table>
686
+ </Sample>
687
+
688
+ <Sample iid="GSM3024935">
689
+ <Status database="GEO">
690
+ <Submission-Date>2018-02-27</Submission-Date>
691
+ <Release-Date>2018-07-23</Release-Date>
692
+ <Last-Update-Date>2018-07-23</Last-Update-Date>
693
+ </Status>
694
+ <Title>PBMC genomic DNA ME/CFS 6</Title>
695
+ <Accession database="GEO">GSM3024935</Accession>
696
+ <Type>genomic</Type>
697
+ <Channel-Count>1</Channel-Count>
698
+ <Channel position="1">
699
+ <Source>ME/CFS PBMC</Source>
700
+ <Organism taxid="9606">Homo sapiens</Organism>
701
+ <Characteristics tag="gender">
702
+ female
703
+ </Characteristics>
704
+ <Characteristics tag="subject id">
705
+ ME/CFS subject 6
706
+ </Characteristics>
707
+ <Characteristics tag="disease state">
708
+ Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS)
709
+ </Characteristics>
710
+ <Characteristics tag="cell type">
711
+ peripheral blood mononuclear cells (PBMC)
712
+ </Characteristics>
713
+ <Molecule>genomic DNA</Molecule>
714
+ <Extract-Protocol>
715
+ genomic DNA was extracted and purified from PBMC samples using Qiagen DNeasy Blood &amp; Tissue Kit according to manufacturer instructions
716
+ </Extract-Protocol>
717
+ <Label>Cy3, Cy5</Label>
718
+ <Label-Protocol>
719
+ Standard Illumina Protocol
720
+ </Label-Protocol>
721
+ </Channel>
722
+ <Hybridization-Protocol>
723
+ bisulphite converted DNA was hybridised to Illumina Infinium MethylationEPIC Beadchip using standard Illumina protocol
724
+ </Hybridization-Protocol>
725
+ <Scan-Protocol>
726
+ Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting
727
+ </Scan-Protocol>
728
+ <Description>
729
+ PBMC genomic DNA from ME/CFS subject 6
730
+ </Description>
731
+ <Data-Processing>
732
+ Illumina Genome Studio; Matrix signal intensities contains unmethylated and methylated signal intensities; Matrix processed contains non-normalized average beta values.
733
+ </Data-Processing>
734
+ <Platform-Ref ref="GPL21145" />
735
+ <Contact-Ref ref="contrib1" />
736
+ <Supplementary-Data type="unknown">
737
+ NONE
738
+ </Supplementary-Data>
739
+ <Data-Table>
740
+ <Column position="1">
741
+ <Name>ID_REF</Name>
742
+ </Column>
743
+ <Column position="2">
744
+ <Name>VALUE</Name>
745
+ <Description>Average Beta</Description>
746
+ </Column>
747
+ <Column position="3">
748
+ <Name>Detection Pval</Name>
749
+ </Column>
750
+ <External-Data rows="866895">
751
+ GSM3024935-tbl-1.txt
752
+ </External-Data>
753
+ </Data-Table>
754
+ </Sample>
755
+
756
+ <Sample iid="GSM3024936">
757
+ <Status database="GEO">
758
+ <Submission-Date>2018-02-27</Submission-Date>
759
+ <Release-Date>2018-07-23</Release-Date>
760
+ <Last-Update-Date>2018-07-23</Last-Update-Date>
761
+ </Status>
762
+ <Title>PBMC genomic DNA ME/CFS 7</Title>
763
+ <Accession database="GEO">GSM3024936</Accession>
764
+ <Type>genomic</Type>
765
+ <Channel-Count>1</Channel-Count>
766
+ <Channel position="1">
767
+ <Source>ME/CFS PBMC</Source>
768
+ <Organism taxid="9606">Homo sapiens</Organism>
769
+ <Characteristics tag="gender">
770
+ female
771
+ </Characteristics>
772
+ <Characteristics tag="subject id">
773
+ ME/CFS subject 7
774
+ </Characteristics>
775
+ <Characteristics tag="disease state">
776
+ Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS)
777
+ </Characteristics>
778
+ <Characteristics tag="cell type">
779
+ peripheral blood mononuclear cells (PBMC)
780
+ </Characteristics>
781
+ <Molecule>genomic DNA</Molecule>
782
+ <Extract-Protocol>
783
+ genomic DNA was extracted and purified from PBMC samples using Qiagen DNeasy Blood &amp; Tissue Kit according to manufacturer instructions
784
+ </Extract-Protocol>
785
+ <Label>Cy3, Cy5</Label>
786
+ <Label-Protocol>
787
+ Standard Illumina Protocol
788
+ </Label-Protocol>
789
+ </Channel>
790
+ <Hybridization-Protocol>
791
+ bisulphite converted DNA was hybridised to Illumina Infinium MethylationEPIC Beadchip using standard Illumina protocol
792
+ </Hybridization-Protocol>
793
+ <Scan-Protocol>
794
+ Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting
795
+ </Scan-Protocol>
796
+ <Description>
797
+ PBMC genomic DNA from ME/CFS subject 7
798
+ </Description>
799
+ <Data-Processing>
800
+ Illumina Genome Studio; Matrix signal intensities contains unmethylated and methylated signal intensities; Matrix processed contains non-normalized average beta values.
801
+ </Data-Processing>
802
+ <Platform-Ref ref="GPL21145" />
803
+ <Contact-Ref ref="contrib1" />
804
+ <Supplementary-Data type="unknown">
805
+ NONE
806
+ </Supplementary-Data>
807
+ <Data-Table>
808
+ <Column position="1">
809
+ <Name>ID_REF</Name>
810
+ </Column>
811
+ <Column position="2">
812
+ <Name>VALUE</Name>
813
+ <Description>Average Beta</Description>
814
+ </Column>
815
+ <Column position="3">
816
+ <Name>Detection Pval</Name>
817
+ </Column>
818
+ <External-Data rows="866895">
819
+ GSM3024936-tbl-1.txt
820
+ </External-Data>
821
+ </Data-Table>
822
+ </Sample>
823
+
824
+ <Sample iid="GSM3024937">
825
+ <Status database="GEO">
826
+ <Submission-Date>2018-02-27</Submission-Date>
827
+ <Release-Date>2018-07-23</Release-Date>
828
+ <Last-Update-Date>2018-07-23</Last-Update-Date>
829
+ </Status>
830
+ <Title>PBMC genomic DNA ME/CFS 8</Title>
831
+ <Accession database="GEO">GSM3024937</Accession>
832
+ <Type>genomic</Type>
833
+ <Channel-Count>1</Channel-Count>
834
+ <Channel position="1">
835
+ <Source>ME/CFS PBMC</Source>
836
+ <Organism taxid="9606">Homo sapiens</Organism>
837
+ <Characteristics tag="gender">
838
+ female
839
+ </Characteristics>
840
+ <Characteristics tag="subject id">
841
+ ME/CFS subject 8
842
+ </Characteristics>
843
+ <Characteristics tag="disease state">
844
+ Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS)
845
+ </Characteristics>
846
+ <Characteristics tag="cell type">
847
+ peripheral blood mononuclear cells (PBMC)
848
+ </Characteristics>
849
+ <Molecule>genomic DNA</Molecule>
850
+ <Extract-Protocol>
851
+ genomic DNA was extracted and purified from PBMC samples using Qiagen DNeasy Blood &amp; Tissue Kit according to manufacturer instructions
852
+ </Extract-Protocol>
853
+ <Label>Cy3, Cy5</Label>
854
+ <Label-Protocol>
855
+ Standard Illumina Protocol
856
+ </Label-Protocol>
857
+ </Channel>
858
+ <Hybridization-Protocol>
859
+ bisulphite converted DNA was hybridised to Illumina Infinium MethylationEPIC Beadchip using standard Illumina protocol
860
+ </Hybridization-Protocol>
861
+ <Scan-Protocol>
862
+ Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting
863
+ </Scan-Protocol>
864
+ <Description>
865
+ PBMC genomic DNA from ME/CFS subject 8
866
+ </Description>
867
+ <Data-Processing>
868
+ Illumina Genome Studio; Matrix signal intensities contains unmethylated and methylated signal intensities; Matrix processed contains non-normalized average beta values.
869
+ </Data-Processing>
870
+ <Platform-Ref ref="GPL21145" />
871
+ <Contact-Ref ref="contrib1" />
872
+ <Supplementary-Data type="unknown">
873
+ NONE
874
+ </Supplementary-Data>
875
+ <Data-Table>
876
+ <Column position="1">
877
+ <Name>ID_REF</Name>
878
+ </Column>
879
+ <Column position="2">
880
+ <Name>VALUE</Name>
881
+ <Description>Average Beta</Description>
882
+ </Column>
883
+ <Column position="3">
884
+ <Name>Detection Pval</Name>
885
+ </Column>
886
+ <External-Data rows="866895">
887
+ GSM3024937-tbl-1.txt
888
+ </External-Data>
889
+ </Data-Table>
890
+ </Sample>
891
+
892
+ <Sample iid="GSM3024938">
893
+ <Status database="GEO">
894
+ <Submission-Date>2018-02-27</Submission-Date>
895
+ <Release-Date>2018-07-23</Release-Date>
896
+ <Last-Update-Date>2018-07-23</Last-Update-Date>
897
+ </Status>
898
+ <Title>PBMC genomic DNA Healthy Control (HC) 4</Title>
899
+ <Accession database="GEO">GSM3024938</Accession>
900
+ <Type>genomic</Type>
901
+ <Channel-Count>1</Channel-Count>
902
+ <Channel position="1">
903
+ <Source>HC PBMC</Source>
904
+ <Organism taxid="9606">Homo sapiens</Organism>
905
+ <Characteristics tag="gender">
906
+ female
907
+ </Characteristics>
908
+ <Characteristics tag="subject id">
909
+ HC subject 4
910
+ </Characteristics>
911
+ <Characteristics tag="disease state">
912
+ Healthy Control (HC)
913
+ </Characteristics>
914
+ <Characteristics tag="cell type">
915
+ peripheral blood mononuclear cells (PBMC)
916
+ </Characteristics>
917
+ <Molecule>genomic DNA</Molecule>
918
+ <Extract-Protocol>
919
+ genomic DNA was extracted and purified from PBMC samples using Qiagen DNeasy Blood &amp; Tissue Kit according to manufacturer instructions
920
+ </Extract-Protocol>
921
+ <Label>Cy3, Cy5</Label>
922
+ <Label-Protocol>
923
+ Standard Illumina Protocol
924
+ </Label-Protocol>
925
+ </Channel>
926
+ <Hybridization-Protocol>
927
+ bisulphite converted DNA was hybridised to Illumina Infinium MethylationEPIC Beadchip using standard Illumina protocol
928
+ </Hybridization-Protocol>
929
+ <Scan-Protocol>
930
+ Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting
931
+ </Scan-Protocol>
932
+ <Description>
933
+ PBMC genomic DNA from HC subject 4
934
+ </Description>
935
+ <Data-Processing>
936
+ Illumina Genome Studio; Matrix signal intensities contains unmethylated and methylated signal intensities; Matrix processed contains non-normalized average beta values.
937
+ </Data-Processing>
938
+ <Platform-Ref ref="GPL21145" />
939
+ <Contact-Ref ref="contrib1" />
940
+ <Supplementary-Data type="unknown">
941
+ NONE
942
+ </Supplementary-Data>
943
+ <Data-Table>
944
+ <Column position="1">
945
+ <Name>ID_REF</Name>
946
+ </Column>
947
+ <Column position="2">
948
+ <Name>VALUE</Name>
949
+ <Description>Average Beta</Description>
950
+ </Column>
951
+ <Column position="3">
952
+ <Name>Detection Pval</Name>
953
+ </Column>
954
+ <External-Data rows="866895">
955
+ GSM3024938-tbl-1.txt
956
+ </External-Data>
957
+ </Data-Table>
958
+ </Sample>
959
+
960
+ <Sample iid="GSM3024939">
961
+ <Status database="GEO">
962
+ <Submission-Date>2018-02-27</Submission-Date>
963
+ <Release-Date>2018-07-23</Release-Date>
964
+ <Last-Update-Date>2018-07-23</Last-Update-Date>
965
+ </Status>
966
+ <Title>PBMC genomic DNA Healthy Control (HC) 5</Title>
967
+ <Accession database="GEO">GSM3024939</Accession>
968
+ <Type>genomic</Type>
969
+ <Channel-Count>1</Channel-Count>
970
+ <Channel position="1">
971
+ <Source>HC PBMC</Source>
972
+ <Organism taxid="9606">Homo sapiens</Organism>
973
+ <Characteristics tag="gender">
974
+ female
975
+ </Characteristics>
976
+ <Characteristics tag="subject id">
977
+ HC subject 5
978
+ </Characteristics>
979
+ <Characteristics tag="disease state">
980
+ Healthy Control (HC)
981
+ </Characteristics>
982
+ <Characteristics tag="cell type">
983
+ peripheral blood mononuclear cells (PBMC)
984
+ </Characteristics>
985
+ <Molecule>genomic DNA</Molecule>
986
+ <Extract-Protocol>
987
+ genomic DNA was extracted and purified from PBMC samples using Qiagen DNeasy Blood &amp; Tissue Kit according to manufacturer instructions
988
+ </Extract-Protocol>
989
+ <Label>Cy3, Cy5</Label>
990
+ <Label-Protocol>
991
+ Standard Illumina Protocol
992
+ </Label-Protocol>
993
+ </Channel>
994
+ <Hybridization-Protocol>
995
+ bisulphite converted DNA was hybridised to Illumina Infinium MethylationEPIC Beadchip using standard Illumina protocol
996
+ </Hybridization-Protocol>
997
+ <Scan-Protocol>
998
+ Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting
999
+ </Scan-Protocol>
1000
+ <Description>
1001
+ PBMC genomic DNA from HC subject 5
1002
+ </Description>
1003
+ <Data-Processing>
1004
+ Illumina Genome Studio; Matrix signal intensities contains unmethylated and methylated signal intensities; Matrix processed contains non-normalized average beta values.
1005
+ </Data-Processing>
1006
+ <Platform-Ref ref="GPL21145" />
1007
+ <Contact-Ref ref="contrib1" />
1008
+ <Supplementary-Data type="unknown">
1009
+ NONE
1010
+ </Supplementary-Data>
1011
+ <Data-Table>
1012
+ <Column position="1">
1013
+ <Name>ID_REF</Name>
1014
+ </Column>
1015
+ <Column position="2">
1016
+ <Name>VALUE</Name>
1017
+ <Description>Average Beta</Description>
1018
+ </Column>
1019
+ <Column position="3">
1020
+ <Name>Detection Pval</Name>
1021
+ </Column>
1022
+ <External-Data rows="866895">
1023
+ GSM3024939-tbl-1.txt
1024
+ </External-Data>
1025
+ </Data-Table>
1026
+ </Sample>
1027
+
1028
+ <Sample iid="GSM3024940">
1029
+ <Status database="GEO">
1030
+ <Submission-Date>2018-02-27</Submission-Date>
1031
+ <Release-Date>2018-07-23</Release-Date>
1032
+ <Last-Update-Date>2018-07-23</Last-Update-Date>
1033
+ </Status>
1034
+ <Title>PBMC genomic DNA ME/CFS 9</Title>
1035
+ <Accession database="GEO">GSM3024940</Accession>
1036
+ <Type>genomic</Type>
1037
+ <Channel-Count>1</Channel-Count>
1038
+ <Channel position="1">
1039
+ <Source>ME/CFS PBMC</Source>
1040
+ <Organism taxid="9606">Homo sapiens</Organism>
1041
+ <Characteristics tag="gender">
1042
+ female
1043
+ </Characteristics>
1044
+ <Characteristics tag="subject id">
1045
+ ME/CFS subject 9
1046
+ </Characteristics>
1047
+ <Characteristics tag="disease state">
1048
+ Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS)
1049
+ </Characteristics>
1050
+ <Characteristics tag="cell type">
1051
+ peripheral blood mononuclear cells (PBMC)
1052
+ </Characteristics>
1053
+ <Molecule>genomic DNA</Molecule>
1054
+ <Extract-Protocol>
1055
+ genomic DNA was extracted and purified from PBMC samples using Qiagen DNeasy Blood &amp; Tissue Kit according to manufacturer instructions
1056
+ </Extract-Protocol>
1057
+ <Label>Cy3, Cy5</Label>
1058
+ <Label-Protocol>
1059
+ Standard Illumina Protocol
1060
+ </Label-Protocol>
1061
+ </Channel>
1062
+ <Hybridization-Protocol>
1063
+ bisulphite converted DNA was hybridised to Illumina Infinium MethylationEPIC Beadchip using standard Illumina protocol
1064
+ </Hybridization-Protocol>
1065
+ <Scan-Protocol>
1066
+ Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting
1067
+ </Scan-Protocol>
1068
+ <Description>
1069
+ PBMC genomic DNA from ME/CFS subject 9
1070
+ </Description>
1071
+ <Data-Processing>
1072
+ Illumina Genome Studio; Matrix signal intensities contains unmethylated and methylated signal intensities; Matrix processed contains non-normalized average beta values.
1073
+ </Data-Processing>
1074
+ <Platform-Ref ref="GPL21145" />
1075
+ <Contact-Ref ref="contrib1" />
1076
+ <Supplementary-Data type="unknown">
1077
+ NONE
1078
+ </Supplementary-Data>
1079
+ <Data-Table>
1080
+ <Column position="1">
1081
+ <Name>ID_REF</Name>
1082
+ </Column>
1083
+ <Column position="2">
1084
+ <Name>VALUE</Name>
1085
+ <Description>Average Beta</Description>
1086
+ </Column>
1087
+ <Column position="3">
1088
+ <Name>Detection Pval</Name>
1089
+ </Column>
1090
+ <External-Data rows="866895">
1091
+ GSM3024940-tbl-1.txt
1092
+ </External-Data>
1093
+ </Data-Table>
1094
+ </Sample>
1095
+
1096
+ <Sample iid="GSM3024941">
1097
+ <Status database="GEO">
1098
+ <Submission-Date>2018-02-27</Submission-Date>
1099
+ <Release-Date>2018-07-23</Release-Date>
1100
+ <Last-Update-Date>2018-07-23</Last-Update-Date>
1101
+ </Status>
1102
+ <Title>PBMC genomic DNA Healthy Control (HC) 6</Title>
1103
+ <Accession database="GEO">GSM3024941</Accession>
1104
+ <Type>genomic</Type>
1105
+ <Channel-Count>1</Channel-Count>
1106
+ <Channel position="1">
1107
+ <Source>HC PBMC</Source>
1108
+ <Organism taxid="9606">Homo sapiens</Organism>
1109
+ <Characteristics tag="gender">
1110
+ female
1111
+ </Characteristics>
1112
+ <Characteristics tag="subject id">
1113
+ HC subject 6
1114
+ </Characteristics>
1115
+ <Characteristics tag="disease state">
1116
+ Healthy Control (HC)
1117
+ </Characteristics>
1118
+ <Characteristics tag="cell type">
1119
+ peripheral blood mononuclear cells (PBMC)
1120
+ </Characteristics>
1121
+ <Molecule>genomic DNA</Molecule>
1122
+ <Extract-Protocol>
1123
+ genomic DNA was extracted and purified from PBMC samples using Qiagen DNeasy Blood &amp; Tissue Kit according to manufacturer instructions
1124
+ </Extract-Protocol>
1125
+ <Label>Cy3, Cy5</Label>
1126
+ <Label-Protocol>
1127
+ Standard Illumina Protocol
1128
+ </Label-Protocol>
1129
+ </Channel>
1130
+ <Hybridization-Protocol>
1131
+ bisulphite converted DNA was hybridised to Illumina Infinium MethylationEPIC Beadchip using standard Illumina protocol
1132
+ </Hybridization-Protocol>
1133
+ <Scan-Protocol>
1134
+ Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting
1135
+ </Scan-Protocol>
1136
+ <Description>
1137
+ PBMC genomic DNA from HC subject 6
1138
+ </Description>
1139
+ <Data-Processing>
1140
+ Illumina Genome Studio; Matrix signal intensities contains unmethylated and methylated signal intensities; Matrix processed contains non-normalized average beta values.
1141
+ </Data-Processing>
1142
+ <Platform-Ref ref="GPL21145" />
1143
+ <Contact-Ref ref="contrib1" />
1144
+ <Supplementary-Data type="unknown">
1145
+ NONE
1146
+ </Supplementary-Data>
1147
+ <Data-Table>
1148
+ <Column position="1">
1149
+ <Name>ID_REF</Name>
1150
+ </Column>
1151
+ <Column position="2">
1152
+ <Name>VALUE</Name>
1153
+ <Description>Average Beta</Description>
1154
+ </Column>
1155
+ <Column position="3">
1156
+ <Name>Detection Pval</Name>
1157
+ </Column>
1158
+ <External-Data rows="866895">
1159
+ GSM3024941-tbl-1.txt
1160
+ </External-Data>
1161
+ </Data-Table>
1162
+ </Sample>
1163
+
1164
+ <Sample iid="GSM3024942">
1165
+ <Status database="GEO">
1166
+ <Submission-Date>2018-02-27</Submission-Date>
1167
+ <Release-Date>2018-07-23</Release-Date>
1168
+ <Last-Update-Date>2018-07-23</Last-Update-Date>
1169
+ </Status>
1170
+ <Title>PBMC genomic DNA ME/CFS 10</Title>
1171
+ <Accession database="GEO">GSM3024942</Accession>
1172
+ <Type>genomic</Type>
1173
+ <Channel-Count>1</Channel-Count>
1174
+ <Channel position="1">
1175
+ <Source>ME/CFS PBMC</Source>
1176
+ <Organism taxid="9606">Homo sapiens</Organism>
1177
+ <Characteristics tag="gender">
1178
+ female
1179
+ </Characteristics>
1180
+ <Characteristics tag="subject id">
1181
+ ME/CFS subject 10
1182
+ </Characteristics>
1183
+ <Characteristics tag="disease state">
1184
+ Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS)
1185
+ </Characteristics>
1186
+ <Characteristics tag="cell type">
1187
+ peripheral blood mononuclear cells (PBMC)
1188
+ </Characteristics>
1189
+ <Molecule>genomic DNA</Molecule>
1190
+ <Extract-Protocol>
1191
+ genomic DNA was extracted and purified from PBMC samples using Qiagen DNeasy Blood &amp; Tissue Kit according to manufacturer instructions
1192
+ </Extract-Protocol>
1193
+ <Label>Cy3, Cy5</Label>
1194
+ <Label-Protocol>
1195
+ Standard Illumina Protocol
1196
+ </Label-Protocol>
1197
+ </Channel>
1198
+ <Hybridization-Protocol>
1199
+ bisulphite converted DNA was hybridised to Illumina Infinium MethylationEPIC Beadchip using standard Illumina protocol
1200
+ </Hybridization-Protocol>
1201
+ <Scan-Protocol>
1202
+ Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting
1203
+ </Scan-Protocol>
1204
+ <Description>
1205
+ PBMC genomic DNA from ME/CFS subject 10
1206
+ </Description>
1207
+ <Data-Processing>
1208
+ Illumina Genome Studio; Matrix signal intensities contains unmethylated and methylated signal intensities; Matrix processed contains non-normalized average beta values.
1209
+ </Data-Processing>
1210
+ <Platform-Ref ref="GPL21145" />
1211
+ <Contact-Ref ref="contrib1" />
1212
+ <Supplementary-Data type="unknown">
1213
+ NONE
1214
+ </Supplementary-Data>
1215
+ <Data-Table>
1216
+ <Column position="1">
1217
+ <Name>ID_REF</Name>
1218
+ </Column>
1219
+ <Column position="2">
1220
+ <Name>VALUE</Name>
1221
+ <Description>Average Beta</Description>
1222
+ </Column>
1223
+ <Column position="3">
1224
+ <Name>Detection Pval</Name>
1225
+ </Column>
1226
+ <External-Data rows="866895">
1227
+ GSM3024942-tbl-1.txt
1228
+ </External-Data>
1229
+ </Data-Table>
1230
+ </Sample>
1231
+
1232
+ <Sample iid="GSM3024943">
1233
+ <Status database="GEO">
1234
+ <Submission-Date>2018-02-27</Submission-Date>
1235
+ <Release-Date>2018-07-23</Release-Date>
1236
+ <Last-Update-Date>2018-07-23</Last-Update-Date>
1237
+ </Status>
1238
+ <Title>PBMC genomic DNA Healthy Control (HC) 7</Title>
1239
+ <Accession database="GEO">GSM3024943</Accession>
1240
+ <Type>genomic</Type>
1241
+ <Channel-Count>1</Channel-Count>
1242
+ <Channel position="1">
1243
+ <Source>HC PBMC</Source>
1244
+ <Organism taxid="9606">Homo sapiens</Organism>
1245
+ <Characteristics tag="gender">
1246
+ female
1247
+ </Characteristics>
1248
+ <Characteristics tag="subject id">
1249
+ HC subject 7
1250
+ </Characteristics>
1251
+ <Characteristics tag="disease state">
1252
+ Healthy Control (HC)
1253
+ </Characteristics>
1254
+ <Characteristics tag="cell type">
1255
+ peripheral blood mononuclear cells (PBMC)
1256
+ </Characteristics>
1257
+ <Molecule>genomic DNA</Molecule>
1258
+ <Extract-Protocol>
1259
+ genomic DNA was extracted and purified from PBMC samples using Qiagen DNeasy Blood &amp; Tissue Kit according to manufacturer instructions
1260
+ </Extract-Protocol>
1261
+ <Label>Cy3, Cy5</Label>
1262
+ <Label-Protocol>
1263
+ Standard Illumina Protocol
1264
+ </Label-Protocol>
1265
+ </Channel>
1266
+ <Hybridization-Protocol>
1267
+ bisulphite converted DNA was hybridised to Illumina Infinium MethylationEPIC Beadchip using standard Illumina protocol
1268
+ </Hybridization-Protocol>
1269
+ <Scan-Protocol>
1270
+ Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting
1271
+ </Scan-Protocol>
1272
+ <Description>
1273
+ PBMC genomic DNA from HC subject 7
1274
+ </Description>
1275
+ <Data-Processing>
1276
+ Illumina Genome Studio; Matrix signal intensities contains unmethylated and methylated signal intensities; Matrix processed contains non-normalized average beta values.
1277
+ </Data-Processing>
1278
+ <Platform-Ref ref="GPL21145" />
1279
+ <Contact-Ref ref="contrib1" />
1280
+ <Supplementary-Data type="unknown">
1281
+ NONE
1282
+ </Supplementary-Data>
1283
+ <Data-Table>
1284
+ <Column position="1">
1285
+ <Name>ID_REF</Name>
1286
+ </Column>
1287
+ <Column position="2">
1288
+ <Name>VALUE</Name>
1289
+ <Description>Average Beta</Description>
1290
+ </Column>
1291
+ <Column position="3">
1292
+ <Name>Detection Pval</Name>
1293
+ </Column>
1294
+ <External-Data rows="866895">
1295
+ GSM3024943-tbl-1.txt
1296
+ </External-Data>
1297
+ </Data-Table>
1298
+ </Sample>
1299
+
1300
+ <Sample iid="GSM3024944">
1301
+ <Status database="GEO">
1302
+ <Submission-Date>2018-02-27</Submission-Date>
1303
+ <Release-Date>2018-07-23</Release-Date>
1304
+ <Last-Update-Date>2018-07-23</Last-Update-Date>
1305
+ </Status>
1306
+ <Title>PBMC genomic DNA ME/CFS 11</Title>
1307
+ <Accession database="GEO">GSM3024944</Accession>
1308
+ <Type>genomic</Type>
1309
+ <Channel-Count>1</Channel-Count>
1310
+ <Channel position="1">
1311
+ <Source>ME/CFS PBMC</Source>
1312
+ <Organism taxid="9606">Homo sapiens</Organism>
1313
+ <Characteristics tag="gender">
1314
+ female
1315
+ </Characteristics>
1316
+ <Characteristics tag="subject id">
1317
+ ME/CFS subject 11
1318
+ </Characteristics>
1319
+ <Characteristics tag="disease state">
1320
+ Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS)
1321
+ </Characteristics>
1322
+ <Characteristics tag="cell type">
1323
+ peripheral blood mononuclear cells (PBMC)
1324
+ </Characteristics>
1325
+ <Molecule>genomic DNA</Molecule>
1326
+ <Extract-Protocol>
1327
+ genomic DNA was extracted and purified from PBMC samples using Qiagen DNeasy Blood &amp; Tissue Kit according to manufacturer instructions
1328
+ </Extract-Protocol>
1329
+ <Label>Cy3, Cy5</Label>
1330
+ <Label-Protocol>
1331
+ Standard Illumina Protocol
1332
+ </Label-Protocol>
1333
+ </Channel>
1334
+ <Hybridization-Protocol>
1335
+ bisulphite converted DNA was hybridised to Illumina Infinium MethylationEPIC Beadchip using standard Illumina protocol
1336
+ </Hybridization-Protocol>
1337
+ <Scan-Protocol>
1338
+ Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting
1339
+ </Scan-Protocol>
1340
+ <Description>
1341
+ PBMC genomic DNA from ME/CFS subject 11
1342
+ </Description>
1343
+ <Data-Processing>
1344
+ Illumina Genome Studio; Matrix signal intensities contains unmethylated and methylated signal intensities; Matrix processed contains non-normalized average beta values.
1345
+ </Data-Processing>
1346
+ <Platform-Ref ref="GPL21145" />
1347
+ <Contact-Ref ref="contrib1" />
1348
+ <Supplementary-Data type="unknown">
1349
+ NONE
1350
+ </Supplementary-Data>
1351
+ <Data-Table>
1352
+ <Column position="1">
1353
+ <Name>ID_REF</Name>
1354
+ </Column>
1355
+ <Column position="2">
1356
+ <Name>VALUE</Name>
1357
+ <Description>Average Beta</Description>
1358
+ </Column>
1359
+ <Column position="3">
1360
+ <Name>Detection Pval</Name>
1361
+ </Column>
1362
+ <External-Data rows="866895">
1363
+ GSM3024944-tbl-1.txt
1364
+ </External-Data>
1365
+ </Data-Table>
1366
+ </Sample>
1367
+
1368
+ <Sample iid="GSM3024945">
1369
+ <Status database="GEO">
1370
+ <Submission-Date>2018-02-27</Submission-Date>
1371
+ <Release-Date>2018-07-23</Release-Date>
1372
+ <Last-Update-Date>2018-07-23</Last-Update-Date>
1373
+ </Status>
1374
+ <Title>PBMC genomic DNA Healthy Control (HC) 8</Title>
1375
+ <Accession database="GEO">GSM3024945</Accession>
1376
+ <Type>genomic</Type>
1377
+ <Channel-Count>1</Channel-Count>
1378
+ <Channel position="1">
1379
+ <Source>HC PBMC</Source>
1380
+ <Organism taxid="9606">Homo sapiens</Organism>
1381
+ <Characteristics tag="gender">
1382
+ female
1383
+ </Characteristics>
1384
+ <Characteristics tag="subject id">
1385
+ HC subject 8
1386
+ </Characteristics>
1387
+ <Characteristics tag="disease state">
1388
+ Healthy Control (HC)
1389
+ </Characteristics>
1390
+ <Characteristics tag="cell type">
1391
+ peripheral blood mononuclear cells (PBMC)
1392
+ </Characteristics>
1393
+ <Molecule>genomic DNA</Molecule>
1394
+ <Extract-Protocol>
1395
+ genomic DNA was extracted and purified from PBMC samples using Qiagen DNeasy Blood &amp; Tissue Kit according to manufacturer instructions
1396
+ </Extract-Protocol>
1397
+ <Label>Cy3, Cy5</Label>
1398
+ <Label-Protocol>
1399
+ Standard Illumina Protocol
1400
+ </Label-Protocol>
1401
+ </Channel>
1402
+ <Hybridization-Protocol>
1403
+ bisulphite converted DNA was hybridised to Illumina Infinium MethylationEPIC Beadchip using standard Illumina protocol
1404
+ </Hybridization-Protocol>
1405
+ <Scan-Protocol>
1406
+ Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting
1407
+ </Scan-Protocol>
1408
+ <Description>
1409
+ PBMC genomic DNA from HC subject 8
1410
+ </Description>
1411
+ <Data-Processing>
1412
+ Illumina Genome Studio; Matrix signal intensities contains unmethylated and methylated signal intensities; Matrix processed contains non-normalized average beta values.
1413
+ </Data-Processing>
1414
+ <Platform-Ref ref="GPL21145" />
1415
+ <Contact-Ref ref="contrib1" />
1416
+ <Supplementary-Data type="unknown">
1417
+ NONE
1418
+ </Supplementary-Data>
1419
+ <Data-Table>
1420
+ <Column position="1">
1421
+ <Name>ID_REF</Name>
1422
+ </Column>
1423
+ <Column position="2">
1424
+ <Name>VALUE</Name>
1425
+ <Description>Average Beta</Description>
1426
+ </Column>
1427
+ <Column position="3">
1428
+ <Name>Detection Pval</Name>
1429
+ </Column>
1430
+ <External-Data rows="866895">
1431
+ GSM3024945-tbl-1.txt
1432
+ </External-Data>
1433
+ </Data-Table>
1434
+ </Sample>
1435
+
1436
+ <Sample iid="GSM3024946">
1437
+ <Status database="GEO">
1438
+ <Submission-Date>2018-02-27</Submission-Date>
1439
+ <Release-Date>2018-07-23</Release-Date>
1440
+ <Last-Update-Date>2018-07-23</Last-Update-Date>
1441
+ </Status>
1442
+ <Title>PBMC genomic DNA ME/CFS 12</Title>
1443
+ <Accession database="GEO">GSM3024946</Accession>
1444
+ <Type>genomic</Type>
1445
+ <Channel-Count>1</Channel-Count>
1446
+ <Channel position="1">
1447
+ <Source>ME/CFS PBMC</Source>
1448
+ <Organism taxid="9606">Homo sapiens</Organism>
1449
+ <Characteristics tag="gender">
1450
+ female
1451
+ </Characteristics>
1452
+ <Characteristics tag="subject id">
1453
+ ME/CFS subject 12
1454
+ </Characteristics>
1455
+ <Characteristics tag="disease state">
1456
+ Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS)
1457
+ </Characteristics>
1458
+ <Characteristics tag="cell type">
1459
+ peripheral blood mononuclear cells (PBMC)
1460
+ </Characteristics>
1461
+ <Molecule>genomic DNA</Molecule>
1462
+ <Extract-Protocol>
1463
+ genomic DNA was extracted and purified from PBMC samples using Qiagen DNeasy Blood &amp; Tissue Kit according to manufacturer instructions
1464
+ </Extract-Protocol>
1465
+ <Label>Cy3, Cy5</Label>
1466
+ <Label-Protocol>
1467
+ Standard Illumina Protocol
1468
+ </Label-Protocol>
1469
+ </Channel>
1470
+ <Hybridization-Protocol>
1471
+ bisulphite converted DNA was hybridised to Illumina Infinium MethylationEPIC Beadchip using standard Illumina protocol
1472
+ </Hybridization-Protocol>
1473
+ <Scan-Protocol>
1474
+ Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting
1475
+ </Scan-Protocol>
1476
+ <Description>
1477
+ PBMC genomic DNA from ME/CFS subject 12
1478
+ </Description>
1479
+ <Data-Processing>
1480
+ Illumina Genome Studio; Matrix signal intensities contains unmethylated and methylated signal intensities; Matrix processed contains non-normalized average beta values.
1481
+ </Data-Processing>
1482
+ <Platform-Ref ref="GPL21145" />
1483
+ <Contact-Ref ref="contrib1" />
1484
+ <Supplementary-Data type="unknown">
1485
+ NONE
1486
+ </Supplementary-Data>
1487
+ <Data-Table>
1488
+ <Column position="1">
1489
+ <Name>ID_REF</Name>
1490
+ </Column>
1491
+ <Column position="2">
1492
+ <Name>VALUE</Name>
1493
+ <Description>Average Beta</Description>
1494
+ </Column>
1495
+ <Column position="3">
1496
+ <Name>Detection Pval</Name>
1497
+ </Column>
1498
+ <External-Data rows="866895">
1499
+ GSM3024946-tbl-1.txt
1500
+ </External-Data>
1501
+ </Data-Table>
1502
+ </Sample>
1503
+
1504
+ <Sample iid="GSM3024947">
1505
+ <Status database="GEO">
1506
+ <Submission-Date>2018-02-27</Submission-Date>
1507
+ <Release-Date>2018-07-23</Release-Date>
1508
+ <Last-Update-Date>2018-07-23</Last-Update-Date>
1509
+ </Status>
1510
+ <Title>PBMC genomic DNA Healthy Control (HC) 9</Title>
1511
+ <Accession database="GEO">GSM3024947</Accession>
1512
+ <Type>genomic</Type>
1513
+ <Channel-Count>1</Channel-Count>
1514
+ <Channel position="1">
1515
+ <Source>HC PBMC</Source>
1516
+ <Organism taxid="9606">Homo sapiens</Organism>
1517
+ <Characteristics tag="gender">
1518
+ female
1519
+ </Characteristics>
1520
+ <Characteristics tag="subject id">
1521
+ HC subject 9
1522
+ </Characteristics>
1523
+ <Characteristics tag="disease state">
1524
+ Healthy Control (HC)
1525
+ </Characteristics>
1526
+ <Characteristics tag="cell type">
1527
+ peripheral blood mononuclear cells (PBMC)
1528
+ </Characteristics>
1529
+ <Molecule>genomic DNA</Molecule>
1530
+ <Extract-Protocol>
1531
+ genomic DNA was extracted and purified from PBMC samples using Qiagen DNeasy Blood &amp; Tissue Kit according to manufacturer instructions
1532
+ </Extract-Protocol>
1533
+ <Label>Cy3, Cy5</Label>
1534
+ <Label-Protocol>
1535
+ Standard Illumina Protocol
1536
+ </Label-Protocol>
1537
+ </Channel>
1538
+ <Hybridization-Protocol>
1539
+ bisulphite converted DNA was hybridised to Illumina Infinium MethylationEPIC Beadchip using standard Illumina protocol
1540
+ </Hybridization-Protocol>
1541
+ <Scan-Protocol>
1542
+ Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting
1543
+ </Scan-Protocol>
1544
+ <Description>
1545
+ PBMC genomic DNA from HC subject 9
1546
+ </Description>
1547
+ <Data-Processing>
1548
+ Illumina Genome Studio; Matrix signal intensities contains unmethylated and methylated signal intensities; Matrix processed contains non-normalized average beta values.
1549
+ </Data-Processing>
1550
+ <Platform-Ref ref="GPL21145" />
1551
+ <Contact-Ref ref="contrib1" />
1552
+ <Supplementary-Data type="unknown">
1553
+ NONE
1554
+ </Supplementary-Data>
1555
+ <Data-Table>
1556
+ <Column position="1">
1557
+ <Name>ID_REF</Name>
1558
+ </Column>
1559
+ <Column position="2">
1560
+ <Name>VALUE</Name>
1561
+ <Description>Average Beta</Description>
1562
+ </Column>
1563
+ <Column position="3">
1564
+ <Name>Detection Pval</Name>
1565
+ </Column>
1566
+ <External-Data rows="866895">
1567
+ GSM3024947-tbl-1.txt
1568
+ </External-Data>
1569
+ </Data-Table>
1570
+ </Sample>
1571
+
1572
+ <Sample iid="GSM3024948">
1573
+ <Status database="GEO">
1574
+ <Submission-Date>2018-02-27</Submission-Date>
1575
+ <Release-Date>2018-07-23</Release-Date>
1576
+ <Last-Update-Date>2018-07-23</Last-Update-Date>
1577
+ </Status>
1578
+ <Title>PBMC genomic DNA ME/CFS 13</Title>
1579
+ <Accession database="GEO">GSM3024948</Accession>
1580
+ <Type>genomic</Type>
1581
+ <Channel-Count>1</Channel-Count>
1582
+ <Channel position="1">
1583
+ <Source>ME/CFS PBMC</Source>
1584
+ <Organism taxid="9606">Homo sapiens</Organism>
1585
+ <Characteristics tag="gender">
1586
+ female
1587
+ </Characteristics>
1588
+ <Characteristics tag="subject id">
1589
+ ME/CFS subject 13
1590
+ </Characteristics>
1591
+ <Characteristics tag="disease state">
1592
+ Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS)
1593
+ </Characteristics>
1594
+ <Characteristics tag="cell type">
1595
+ peripheral blood mononuclear cells (PBMC)
1596
+ </Characteristics>
1597
+ <Molecule>genomic DNA</Molecule>
1598
+ <Extract-Protocol>
1599
+ genomic DNA was extracted and purified from PBMC samples using Qiagen DNeasy Blood &amp; Tissue Kit according to manufacturer instructions
1600
+ </Extract-Protocol>
1601
+ <Label>Cy3, Cy5</Label>
1602
+ <Label-Protocol>
1603
+ Standard Illumina Protocol
1604
+ </Label-Protocol>
1605
+ </Channel>
1606
+ <Hybridization-Protocol>
1607
+ bisulphite converted DNA was hybridised to Illumina Infinium MethylationEPIC Beadchip using standard Illumina protocol
1608
+ </Hybridization-Protocol>
1609
+ <Scan-Protocol>
1610
+ Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting
1611
+ </Scan-Protocol>
1612
+ <Description>
1613
+ PBMC genomic DNA from ME/CFS subject 13
1614
+ </Description>
1615
+ <Data-Processing>
1616
+ Illumina Genome Studio; Matrix signal intensities contains unmethylated and methylated signal intensities; Matrix processed contains non-normalized average beta values.
1617
+ </Data-Processing>
1618
+ <Platform-Ref ref="GPL21145" />
1619
+ <Contact-Ref ref="contrib1" />
1620
+ <Supplementary-Data type="unknown">
1621
+ NONE
1622
+ </Supplementary-Data>
1623
+ <Data-Table>
1624
+ <Column position="1">
1625
+ <Name>ID_REF</Name>
1626
+ </Column>
1627
+ <Column position="2">
1628
+ <Name>VALUE</Name>
1629
+ <Description>Average Beta</Description>
1630
+ </Column>
1631
+ <Column position="3">
1632
+ <Name>Detection Pval</Name>
1633
+ </Column>
1634
+ <External-Data rows="866895">
1635
+ GSM3024948-tbl-1.txt
1636
+ </External-Data>
1637
+ </Data-Table>
1638
+ </Sample>
1639
+
1640
+ <Sample iid="GSM3024949">
1641
+ <Status database="GEO">
1642
+ <Submission-Date>2018-02-27</Submission-Date>
1643
+ <Release-Date>2018-07-23</Release-Date>
1644
+ <Last-Update-Date>2018-07-23</Last-Update-Date>
1645
+ </Status>
1646
+ <Title>PBMC genomic DNA Healthy Control (HC) 10</Title>
1647
+ <Accession database="GEO">GSM3024949</Accession>
1648
+ <Type>genomic</Type>
1649
+ <Channel-Count>1</Channel-Count>
1650
+ <Channel position="1">
1651
+ <Source>HC PBMC</Source>
1652
+ <Organism taxid="9606">Homo sapiens</Organism>
1653
+ <Characteristics tag="gender">
1654
+ female
1655
+ </Characteristics>
1656
+ <Characteristics tag="subject id">
1657
+ HC subject 10
1658
+ </Characteristics>
1659
+ <Characteristics tag="disease state">
1660
+ Healthy Control (HC)
1661
+ </Characteristics>
1662
+ <Characteristics tag="cell type">
1663
+ peripheral blood mononuclear cells (PBMC)
1664
+ </Characteristics>
1665
+ <Molecule>genomic DNA</Molecule>
1666
+ <Extract-Protocol>
1667
+ genomic DNA was extracted and purified from PBMC samples using Qiagen DNeasy Blood &amp; Tissue Kit according to manufacturer instructions
1668
+ </Extract-Protocol>
1669
+ <Label>Cy3, Cy5</Label>
1670
+ <Label-Protocol>
1671
+ Standard Illumina Protocol
1672
+ </Label-Protocol>
1673
+ </Channel>
1674
+ <Hybridization-Protocol>
1675
+ bisulphite converted DNA was hybridised to Illumina Infinium MethylationEPIC Beadchip using standard Illumina protocol
1676
+ </Hybridization-Protocol>
1677
+ <Scan-Protocol>
1678
+ Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting
1679
+ </Scan-Protocol>
1680
+ <Description>
1681
+ PBMC genomic DNA from HC subject 10
1682
+ </Description>
1683
+ <Data-Processing>
1684
+ Illumina Genome Studio; Matrix signal intensities contains unmethylated and methylated signal intensities; Matrix processed contains non-normalized average beta values.
1685
+ </Data-Processing>
1686
+ <Platform-Ref ref="GPL21145" />
1687
+ <Contact-Ref ref="contrib1" />
1688
+ <Supplementary-Data type="unknown">
1689
+ NONE
1690
+ </Supplementary-Data>
1691
+ <Data-Table>
1692
+ <Column position="1">
1693
+ <Name>ID_REF</Name>
1694
+ </Column>
1695
+ <Column position="2">
1696
+ <Name>VALUE</Name>
1697
+ <Description>Average Beta</Description>
1698
+ </Column>
1699
+ <Column position="3">
1700
+ <Name>Detection Pval</Name>
1701
+ </Column>
1702
+ <External-Data rows="866895">
1703
+ GSM3024949-tbl-1.txt
1704
+ </External-Data>
1705
+ </Data-Table>
1706
+ </Sample>
1707
+
1708
+ <Sample iid="GSM3024950">
1709
+ <Status database="GEO">
1710
+ <Submission-Date>2018-02-27</Submission-Date>
1711
+ <Release-Date>2018-07-23</Release-Date>
1712
+ <Last-Update-Date>2018-07-23</Last-Update-Date>
1713
+ </Status>
1714
+ <Title>PBMC genomic DNA Healthy Control (HC) 11</Title>
1715
+ <Accession database="GEO">GSM3024950</Accession>
1716
+ <Type>genomic</Type>
1717
+ <Channel-Count>1</Channel-Count>
1718
+ <Channel position="1">
1719
+ <Source>HC PBMC</Source>
1720
+ <Organism taxid="9606">Homo sapiens</Organism>
1721
+ <Characteristics tag="gender">
1722
+ female
1723
+ </Characteristics>
1724
+ <Characteristics tag="subject id">
1725
+ HC subject 11
1726
+ </Characteristics>
1727
+ <Characteristics tag="disease state">
1728
+ Healthy Control (HC)
1729
+ </Characteristics>
1730
+ <Characteristics tag="cell type">
1731
+ peripheral blood mononuclear cells (PBMC)
1732
+ </Characteristics>
1733
+ <Molecule>genomic DNA</Molecule>
1734
+ <Extract-Protocol>
1735
+ genomic DNA was extracted and purified from PBMC samples using Qiagen DNeasy Blood &amp; Tissue Kit according to manufacturer instructions
1736
+ </Extract-Protocol>
1737
+ <Label>Cy3, Cy5</Label>
1738
+ <Label-Protocol>
1739
+ Standard Illumina Protocol
1740
+ </Label-Protocol>
1741
+ </Channel>
1742
+ <Hybridization-Protocol>
1743
+ bisulphite converted DNA was hybridised to Illumina Infinium MethylationEPIC Beadchip using standard Illumina protocol
1744
+ </Hybridization-Protocol>
1745
+ <Scan-Protocol>
1746
+ Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting
1747
+ </Scan-Protocol>
1748
+ <Description>
1749
+ PBMC genomic DNA from HC subject 11
1750
+ </Description>
1751
+ <Data-Processing>
1752
+ Illumina Genome Studio; Matrix signal intensities contains unmethylated and methylated signal intensities; Matrix processed contains non-normalized average beta values.
1753
+ </Data-Processing>
1754
+ <Platform-Ref ref="GPL21145" />
1755
+ <Contact-Ref ref="contrib1" />
1756
+ <Supplementary-Data type="unknown">
1757
+ NONE
1758
+ </Supplementary-Data>
1759
+ <Data-Table>
1760
+ <Column position="1">
1761
+ <Name>ID_REF</Name>
1762
+ </Column>
1763
+ <Column position="2">
1764
+ <Name>VALUE</Name>
1765
+ <Description>Average Beta</Description>
1766
+ </Column>
1767
+ <Column position="3">
1768
+ <Name>Detection Pval</Name>
1769
+ </Column>
1770
+ <External-Data rows="866895">
1771
+ GSM3024950-tbl-1.txt
1772
+ </External-Data>
1773
+ </Data-Table>
1774
+ </Sample>
1775
+
1776
+ <Sample iid="GSM3024951">
1777
+ <Status database="GEO">
1778
+ <Submission-Date>2018-02-27</Submission-Date>
1779
+ <Release-Date>2018-07-23</Release-Date>
1780
+ <Last-Update-Date>2018-07-23</Last-Update-Date>
1781
+ </Status>
1782
+ <Title>PBMC genomic DNA Healthy Control (HC) 12</Title>
1783
+ <Accession database="GEO">GSM3024951</Accession>
1784
+ <Type>genomic</Type>
1785
+ <Channel-Count>1</Channel-Count>
1786
+ <Channel position="1">
1787
+ <Source>HC PBMC</Source>
1788
+ <Organism taxid="9606">Homo sapiens</Organism>
1789
+ <Characteristics tag="gender">
1790
+ female
1791
+ </Characteristics>
1792
+ <Characteristics tag="subject id">
1793
+ HC subject 12
1794
+ </Characteristics>
1795
+ <Characteristics tag="disease state">
1796
+ Healthy Control (HC)
1797
+ </Characteristics>
1798
+ <Characteristics tag="cell type">
1799
+ peripheral blood mononuclear cells (PBMC)
1800
+ </Characteristics>
1801
+ <Molecule>genomic DNA</Molecule>
1802
+ <Extract-Protocol>
1803
+ genomic DNA was extracted and purified from PBMC samples using Qiagen DNeasy Blood &amp; Tissue Kit according to manufacturer instructions
1804
+ </Extract-Protocol>
1805
+ <Label>Cy3, Cy5</Label>
1806
+ <Label-Protocol>
1807
+ Standard Illumina Protocol
1808
+ </Label-Protocol>
1809
+ </Channel>
1810
+ <Hybridization-Protocol>
1811
+ bisulphite converted DNA was hybridised to Illumina Infinium MethylationEPIC Beadchip using standard Illumina protocol
1812
+ </Hybridization-Protocol>
1813
+ <Scan-Protocol>
1814
+ Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting
1815
+ </Scan-Protocol>
1816
+ <Description>
1817
+ PBMC genomic DNA from HC subject 12
1818
+ </Description>
1819
+ <Data-Processing>
1820
+ Illumina Genome Studio; Matrix signal intensities contains unmethylated and methylated signal intensities; Matrix processed contains non-normalized average beta values.
1821
+ </Data-Processing>
1822
+ <Platform-Ref ref="GPL21145" />
1823
+ <Contact-Ref ref="contrib1" />
1824
+ <Supplementary-Data type="unknown">
1825
+ NONE
1826
+ </Supplementary-Data>
1827
+ <Data-Table>
1828
+ <Column position="1">
1829
+ <Name>ID_REF</Name>
1830
+ </Column>
1831
+ <Column position="2">
1832
+ <Name>VALUE</Name>
1833
+ <Description>Average Beta</Description>
1834
+ </Column>
1835
+ <Column position="3">
1836
+ <Name>Detection Pval</Name>
1837
+ </Column>
1838
+ <External-Data rows="866895">
1839
+ GSM3024951-tbl-1.txt
1840
+ </External-Data>
1841
+ </Data-Table>
1842
+ </Sample>
1843
+
1844
+ <Series iid="GSE111183">
1845
+ <Status database="GEO">
1846
+ <Submission-Date>2018-02-27</Submission-Date>
1847
+ <Release-Date>2018-07-23</Release-Date>
1848
+ <Last-Update-Date>2019-01-20</Last-Update-Date>
1849
+ </Status>
1850
+ <Title>Identification of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome-associated DNA methylation patterns</Title>
1851
+ <Accession database="GEO">GSE111183</Accession>
1852
+ <Pubmed-ID>30036399</Pubmed-ID>
1853
+ <Summary>
1854
+ Background: Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) is a complex condition that involves multiple organ systems and is characterized by an abrupt or delayed onset of persistent/relapsing symptomatology such as debilitating fatigue, immune dysfunction, neurological problems, and other symptoms not curable for at least 6 months. Disruption of DNA methylation patterns has been tied to various immune and neurological diseases; however, the status of this epigenetic mark in ME/CFS remains uncertain. This study aimed at identifying changes in the DNA methylation patterns that are causative of changes in the regulation of gene expression in ME/CSF patients. Such changes may be also used for diagnostic purposes and be indicative of potential therapeutic targets.
1855
+ Methods: Peripheral blood mononuclear cells (PBMCs) from 13 ME/CFS patients and 12 healthy controls (HC) were used to extract genomic DNA and measure global DNA methylation, and the methylation status at 850,000 CpG sites was assessed using Illumina MethylationEPIC microarrays.
1856
+ Results: Global DNA methylation levels of ME/CFS patients were similar to those of HC. However, microarray-based genome-wide technology allowed detection of 17,296 differentially methylated CpG sites in 6,368 genes across promoters, gene regulatory elements and within coding regions of genes. Analysis of DNA methylation in promoter regions found 307 differentially methylated promoters (DMP); genes associated with DMP participate in at least 15 different pathways mostly related to cell signaling with a strong immune component.
1857
+ Conclusions: This is the first study that has explored genome-wide epigenetic changes associated with ME/CFS using the new MethylationEPIC microarrays covering about 850,000 CpG sites. Our results are consistent with dysregulation of the immune system in ME/CFS and suggest a role of this epigenetic modification on the DNA pathobiology of ME/CFS.
1858
+ </Summary>
1859
+ <Overall-Design>
1860
+ Genomic DNA from 25 peripheral blood mononuclear cells (PBMC) samples (13 ME/CFS, 12 controls) were bisulfite-converted and hybridised to the Illumina MethylationEPIC microarrays. GenomeStudio idat files were generated and the data was analyzed using the RnBeads R package.
1861
+ </Overall-Design>
1862
+ <Type>Methylation profiling by array</Type>
1863
+ <Contributor-Ref ref="contrib3" position="1" />
1864
+ <Contributor-Ref ref="contrib4" position="2" />
1865
+ <Contributor-Ref ref="contrib5" position="3" />
1866
+ <Contributor-Ref ref="contrib6" position="4" />
1867
+ <Contributor-Ref ref="contrib7" position="5" />
1868
+ <Contributor-Ref ref="contrib8" position="6" />
1869
+ <Contributor-Ref ref="contrib9" position="7" />
1870
+ <Contributor-Ref ref="contrib1" position="8" />
1871
+ <Contact-Ref ref="contrib1" />
1872
+ <Sample-Ref ref="GSM3024927" />
1873
+ <Sample-Ref ref="GSM3024928" />
1874
+ <Sample-Ref ref="GSM3024929" />
1875
+ <Sample-Ref ref="GSM3024930" />
1876
+ <Sample-Ref ref="GSM3024931" />
1877
+ <Sample-Ref ref="GSM3024932" />
1878
+ <Sample-Ref ref="GSM3024933" />
1879
+ <Sample-Ref ref="GSM3024934" />
1880
+ <Sample-Ref ref="GSM3024935" />
1881
+ <Sample-Ref ref="GSM3024936" />
1882
+ <Sample-Ref ref="GSM3024937" />
1883
+ <Sample-Ref ref="GSM3024938" />
1884
+ <Sample-Ref ref="GSM3024939" />
1885
+ <Sample-Ref ref="GSM3024940" />
1886
+ <Sample-Ref ref="GSM3024941" />
1887
+ <Sample-Ref ref="GSM3024942" />
1888
+ <Sample-Ref ref="GSM3024943" />
1889
+ <Sample-Ref ref="GSM3024944" />
1890
+ <Sample-Ref ref="GSM3024945" />
1891
+ <Sample-Ref ref="GSM3024946" />
1892
+ <Sample-Ref ref="GSM3024947" />
1893
+ <Sample-Ref ref="GSM3024948" />
1894
+ <Sample-Ref ref="GSM3024949" />
1895
+ <Sample-Ref ref="GSM3024950" />
1896
+ <Sample-Ref ref="GSM3024951" />
1897
+ <Supplementary-Data type="TAR">
1898
+ ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE111nnn/GSE111183/suppl/GSE111183_RAW.tar
1899
+ </Supplementary-Data>
1900
+ <Supplementary-Data type="TXT">
1901
+ ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE111nnn/GSE111183/suppl/GSE111183_signal_intensities.txt.gz
1902
+ </Supplementary-Data>
1903
+ <Relation type="BioProject" target="https://www.ncbi.nlm.nih.gov/bioproject/PRJNA436126" />
1904
+ </Series>
1905
+
1906
+ </MINiML>
ME/GSE153667/GSE153667_RAW/GSM4649028_Control2_CpG.txt ADDED
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ME/GSE153667/GSE153667_RAW/GSM4649033_Control7_CpG.txt ADDED
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ME/GSE153667/GSE153667_RAW/GSM4649045_Patient9_CpG.txt ADDED
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ME/GSE153667/meta/._GSE153667_family.soft ADDED
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ME/GSE153667/meta/._GSE153667_family.xml ADDED
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ME/GSE153667/meta/._GSE153667_series_matrix.txt ADDED
Binary file (4.1 kB). View file
 
ME/GSE153667/meta/GSE153667_family.soft ADDED
@@ -0,0 +1,853 @@
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
1
+ ^DATABASE = GeoMiame
2
+ !Database_name = Gene Expression Omnibus (GEO)
3
+ !Database_institute = NCBI NLM NIH
4
+ !Database_web_link = http://www.ncbi.nlm.nih.gov/geo
5
+ !Database_email = geo@ncbi.nlm.nih.gov
6
+ ^SERIES = GSE153667
7
+ !Series_title = Changes in the Epigenetic Landscape of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Reflect Systemic Dysfunctions
8
+ !Series_geo_accession = GSE153667
9
+ !Series_status = Public on Jul 02 2020
10
+ !Series_submission_date = Jul 01 2020
11
+ !Series_last_update_date = Nov 09 2020
12
+ !Series_pubmed_id = 33148325
13
+ !Series_summary = Purpose: ME/CFS is a lifelong debilitating disease that affects approximately 1% of the global population. Previous studies have identified dysfunctional activity in metabolic, immune and neurological pathways. The goal of this study is to identify ME/CFS specific variations in DNA methylation to determine whether the patient specific epigenetic patterns provide insight into the disease pathophysiology.
14
+ !Series_summary = Methods: DNA was extracted from the PBMCs of 10 ME/CFS patients and age/gender matched controls. After performing RRBS the sequence was aligned to hg19 genome using Bismark. The data was analyzed using first an ANOVA F test through DMAP in order to determine variation between the patient and control groups across 40-220bp fragments of the genome. Additional analysis was performed following a MethylKit pipeline, which analyzed the variation on a single CpG basis using a Fishers test.
15
+ !Series_summary = Results: From a total of 146,575 DMAP fragments we identified 76 differentially methylated fragments (P <0.05, Diff meth +/- 15%). A total of 31 were associated with gene regions (intronic/exonic). MethylKit analysis also identified a total of 394 differentially methylated cytosines (FDR corrected P <0.05, Diff meth +/- 15%) from a total of 196,172 individual analyzed cytosines, 91 of the statistically significant cytosines fell within gene regions. Comparison of both methylomes and regions where both the DMAP fragments and multiple MethylKit cytosines fell highlighted areas of the genome containing regulatory elements associated with metabolic and immune activity. Gene body pathway enrichment additionally identified immune metabolic and neurological related functions.
16
+ !Series_summary = Conclusions: Our study represents the first investigation of ME/CFS patients using reduced representation bisulfite sequencing. We identified a number of major differences between patients that distinguished them from healthy controls. Our results identified a number of differentially methylated regulatory elements and gene bodies that highlight the disturbed pathophysiology in ME/CFS. In particular the large number of enriched neurotransmitter and neuropeptide reactome pathways highlighted a disturbed neurological pathophysiology in patients.
17
+ !Series_overall_design = RRBS Analysis of 10 ME/CFS patients vs. Controls
18
+ !Series_type = Methylation profiling by high throughput sequencing
19
+ !Series_contributor = Amber,,Helliwell
20
+ !Series_contributor = Warren,,Tate
21
+ !Series_contributor = Aniruddha,,Chatterjee
22
+ !Series_contributor = Peter,,Stockwell
23
+ !Series_contributor = Eiren,,Sweetman
24
+ !Series_contributor = Tina,,Edgar
25
+ !Series_sample_id = GSM4649027
26
+ !Series_sample_id = GSM4649028
27
+ !Series_sample_id = GSM4649029
28
+ !Series_sample_id = GSM4649030
29
+ !Series_sample_id = GSM4649031
30
+ !Series_sample_id = GSM4649032
31
+ !Series_sample_id = GSM4649033
32
+ !Series_sample_id = GSM4649034
33
+ !Series_sample_id = GSM4649035
34
+ !Series_sample_id = GSM4649036
35
+ !Series_sample_id = GSM4649037
36
+ !Series_sample_id = GSM4649038
37
+ !Series_sample_id = GSM4649039
38
+ !Series_sample_id = GSM4649040
39
+ !Series_sample_id = GSM4649041
40
+ !Series_sample_id = GSM4649042
41
+ !Series_sample_id = GSM4649043
42
+ !Series_sample_id = GSM4649044
43
+ !Series_sample_id = GSM4649045
44
+ !Series_sample_id = GSM4649046
45
+ !Series_contact_name = Amber,,Helliwell
46
+ !Series_contact_department = Biochemistry Department
47
+ !Series_contact_institute = University of Otago
48
+ !Series_contact_address = 710 Cumberland Road
49
+ !Series_contact_city = Dunedin
50
+ !Series_contact_zip/postal_code = 9016
51
+ !Series_contact_country = New Zealand
52
+ !Series_supplementary_file = ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE153nnn/GSE153667/suppl/GSE153667_DMAP_matrix.csv.gz
53
+ !Series_supplementary_file = ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE153nnn/GSE153667/suppl/GSE153667_GeneMatrix.xlsx
54
+ !Series_supplementary_file = ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE153nnn/GSE153667/suppl/GSE153667_Meth_Matrix.csv.gz
55
+ !Series_supplementary_file = ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE153nnn/GSE153667/suppl/GSE153667_RAW.tar
56
+ !Series_platform_id = GPL16791
57
+ !Series_platform_taxid = 9606
58
+ !Series_sample_taxid = 9606
59
+ !Series_relation = BioProject: https://www.ncbi.nlm.nih.gov/bioproject/PRJNA643579
60
+ !Series_relation = SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRP269624
61
+ ^PLATFORM = GPL16791
62
+ !Platform_title = Illumina HiSeq 2500 (Homo sapiens)
63
+ !Platform_geo_accession = GPL16791
64
+ !Platform_status = Public on Mar 14 2013
65
+ !Platform_submission_date = Mar 14 2013
66
+ !Platform_last_update_date = Mar 27 2019
67
+ !Platform_technology = high-throughput sequencing
68
+ !Platform_distribution = virtual
69
+ !Platform_organism = Homo sapiens
70
+ !Platform_taxid = 9606
71
+ !Platform_contact_name = ,,GEO
72
+ !Platform_contact_country = USA
73
+ !Platform_data_row_count = 0
74
+ ^SAMPLE = GSM4649027
75
+ !Sample_title = Control1
76
+ !Sample_geo_accession = GSM4649027
77
+ !Sample_status = Public on Jul 02 2020
78
+ !Sample_submission_date = Jul 01 2020
79
+ !Sample_last_update_date = Jul 02 2020
80
+ !Sample_type = SRA
81
+ !Sample_channel_count = 1
82
+ !Sample_source_name_ch1 = Peripheral Blood Mononuclear Cells
83
+ !Sample_organism_ch1 = Homo sapiens
84
+ !Sample_taxid_ch1 = 9606
85
+ !Sample_characteristics_ch1 = disease state: Control
86
+ !Sample_molecule_ch1 = genomic DNA
87
+ !Sample_extract_protocol_ch1 = DNA was extracted from 200ul of PBMCs
88
+ !Sample_extract_protocol_ch1 = MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
89
+ !Sample_data_processing = reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
90
+ !Sample_data_processing = reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
91
+ !Sample_data_processing = bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
92
+ !Sample_data_processing = the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data
93
+ !Sample_data_processing = Genome_build: hg19
94
+ !Sample_data_processing = Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline.
95
+ !Sample_data_processing = Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). .
96
+ !Sample_platform_id = GPL16791
97
+ !Sample_contact_name = Amber,,Helliwell
98
+ !Sample_contact_department = Biochemistry Department
99
+ !Sample_contact_institute = University of Otago
100
+ !Sample_contact_address = 710 Cumberland Road
101
+ !Sample_contact_city = Dunedin
102
+ !Sample_contact_zip/postal_code = 9016
103
+ !Sample_contact_country = New Zealand
104
+ !Sample_instrument_model = Illumina HiSeq 2500
105
+ !Sample_library_selection = Reduced Representation
106
+ !Sample_library_source = genomic
107
+ !Sample_library_strategy = Bisulfite-Seq
108
+ !Sample_relation = BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN15420272
109
+ !Sample_relation = SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX8651460
110
+ !Sample_supplementary_file_1 = ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649027/suppl/GSM4649027_Control1_CpG.txt.gz
111
+ !Sample_series_id = GSE153667
112
+ !Sample_data_row_count = 0
113
+ ^SAMPLE = GSM4649028
114
+ !Sample_title = Control2
115
+ !Sample_geo_accession = GSM4649028
116
+ !Sample_status = Public on Jul 02 2020
117
+ !Sample_submission_date = Jul 01 2020
118
+ !Sample_last_update_date = Jul 02 2020
119
+ !Sample_type = SRA
120
+ !Sample_channel_count = 1
121
+ !Sample_source_name_ch1 = Peripheral Blood Mononuclear Cells
122
+ !Sample_organism_ch1 = Homo sapiens
123
+ !Sample_taxid_ch1 = 9606
124
+ !Sample_characteristics_ch1 = disease state: Control
125
+ !Sample_molecule_ch1 = genomic DNA
126
+ !Sample_extract_protocol_ch1 = DNA was extracted from 200ul of PBMCs
127
+ !Sample_extract_protocol_ch1 = MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
128
+ !Sample_data_processing = reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
129
+ !Sample_data_processing = reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
130
+ !Sample_data_processing = bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
131
+ !Sample_data_processing = the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data
132
+ !Sample_data_processing = Genome_build: hg19
133
+ !Sample_data_processing = Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline.
134
+ !Sample_data_processing = Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). .
135
+ !Sample_platform_id = GPL16791
136
+ !Sample_contact_name = Amber,,Helliwell
137
+ !Sample_contact_department = Biochemistry Department
138
+ !Sample_contact_institute = University of Otago
139
+ !Sample_contact_address = 710 Cumberland Road
140
+ !Sample_contact_city = Dunedin
141
+ !Sample_contact_zip/postal_code = 9016
142
+ !Sample_contact_country = New Zealand
143
+ !Sample_instrument_model = Illumina HiSeq 2500
144
+ !Sample_library_selection = Reduced Representation
145
+ !Sample_library_source = genomic
146
+ !Sample_library_strategy = Bisulfite-Seq
147
+ !Sample_relation = BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN15420271
148
+ !Sample_relation = SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX8651461
149
+ !Sample_supplementary_file_1 = ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649028/suppl/GSM4649028_Control2_CpG.txt.gz
150
+ !Sample_series_id = GSE153667
151
+ !Sample_data_row_count = 0
152
+ ^SAMPLE = GSM4649029
153
+ !Sample_title = Control3
154
+ !Sample_geo_accession = GSM4649029
155
+ !Sample_status = Public on Jul 02 2020
156
+ !Sample_submission_date = Jul 01 2020
157
+ !Sample_last_update_date = Jul 02 2020
158
+ !Sample_type = SRA
159
+ !Sample_channel_count = 1
160
+ !Sample_source_name_ch1 = Peripheral Blood Mononuclear Cells
161
+ !Sample_organism_ch1 = Homo sapiens
162
+ !Sample_taxid_ch1 = 9606
163
+ !Sample_characteristics_ch1 = disease state: Control
164
+ !Sample_molecule_ch1 = genomic DNA
165
+ !Sample_extract_protocol_ch1 = DNA was extracted from 200ul of PBMCs
166
+ !Sample_extract_protocol_ch1 = MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
167
+ !Sample_data_processing = reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
168
+ !Sample_data_processing = reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
169
+ !Sample_data_processing = bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
170
+ !Sample_data_processing = the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data
171
+ !Sample_data_processing = Genome_build: hg19
172
+ !Sample_data_processing = Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline.
173
+ !Sample_data_processing = Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). .
174
+ !Sample_platform_id = GPL16791
175
+ !Sample_contact_name = Amber,,Helliwell
176
+ !Sample_contact_department = Biochemistry Department
177
+ !Sample_contact_institute = University of Otago
178
+ !Sample_contact_address = 710 Cumberland Road
179
+ !Sample_contact_city = Dunedin
180
+ !Sample_contact_zip/postal_code = 9016
181
+ !Sample_contact_country = New Zealand
182
+ !Sample_instrument_model = Illumina HiSeq 2500
183
+ !Sample_library_selection = Reduced Representation
184
+ !Sample_library_source = genomic
185
+ !Sample_library_strategy = Bisulfite-Seq
186
+ !Sample_relation = BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN15420270
187
+ !Sample_relation = SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX8651462
188
+ !Sample_supplementary_file_1 = ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649029/suppl/GSM4649029_Control3_CpG.txt.gz
189
+ !Sample_series_id = GSE153667
190
+ !Sample_data_row_count = 0
191
+ ^SAMPLE = GSM4649030
192
+ !Sample_title = Control4
193
+ !Sample_geo_accession = GSM4649030
194
+ !Sample_status = Public on Jul 02 2020
195
+ !Sample_submission_date = Jul 01 2020
196
+ !Sample_last_update_date = Jul 02 2020
197
+ !Sample_type = SRA
198
+ !Sample_channel_count = 1
199
+ !Sample_source_name_ch1 = Peripheral Blood Mononuclear Cells
200
+ !Sample_organism_ch1 = Homo sapiens
201
+ !Sample_taxid_ch1 = 9606
202
+ !Sample_characteristics_ch1 = disease state: Control
203
+ !Sample_molecule_ch1 = genomic DNA
204
+ !Sample_extract_protocol_ch1 = DNA was extracted from 200ul of PBMCs
205
+ !Sample_extract_protocol_ch1 = MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
206
+ !Sample_data_processing = reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
207
+ !Sample_data_processing = reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
208
+ !Sample_data_processing = bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
209
+ !Sample_data_processing = the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data
210
+ !Sample_data_processing = Genome_build: hg19
211
+ !Sample_data_processing = Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline.
212
+ !Sample_data_processing = Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). .
213
+ !Sample_platform_id = GPL16791
214
+ !Sample_contact_name = Amber,,Helliwell
215
+ !Sample_contact_department = Biochemistry Department
216
+ !Sample_contact_institute = University of Otago
217
+ !Sample_contact_address = 710 Cumberland Road
218
+ !Sample_contact_city = Dunedin
219
+ !Sample_contact_zip/postal_code = 9016
220
+ !Sample_contact_country = New Zealand
221
+ !Sample_instrument_model = Illumina HiSeq 2500
222
+ !Sample_library_selection = Reduced Representation
223
+ !Sample_library_source = genomic
224
+ !Sample_library_strategy = Bisulfite-Seq
225
+ !Sample_relation = BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN15420269
226
+ !Sample_relation = SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX8651463
227
+ !Sample_supplementary_file_1 = ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649030/suppl/GSM4649030_Control4_CpG.txt.gz
228
+ !Sample_series_id = GSE153667
229
+ !Sample_data_row_count = 0
230
+ ^SAMPLE = GSM4649031
231
+ !Sample_title = Control5
232
+ !Sample_geo_accession = GSM4649031
233
+ !Sample_status = Public on Jul 02 2020
234
+ !Sample_submission_date = Jul 01 2020
235
+ !Sample_last_update_date = Jul 02 2020
236
+ !Sample_type = SRA
237
+ !Sample_channel_count = 1
238
+ !Sample_source_name_ch1 = Peripheral Blood Mononuclear Cells
239
+ !Sample_organism_ch1 = Homo sapiens
240
+ !Sample_taxid_ch1 = 9606
241
+ !Sample_characteristics_ch1 = disease state: Control
242
+ !Sample_molecule_ch1 = genomic DNA
243
+ !Sample_extract_protocol_ch1 = DNA was extracted from 200ul of PBMCs
244
+ !Sample_extract_protocol_ch1 = MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
245
+ !Sample_data_processing = reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
246
+ !Sample_data_processing = reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
247
+ !Sample_data_processing = bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
248
+ !Sample_data_processing = the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data
249
+ !Sample_data_processing = Genome_build: hg19
250
+ !Sample_data_processing = Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline.
251
+ !Sample_data_processing = Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). .
252
+ !Sample_platform_id = GPL16791
253
+ !Sample_contact_name = Amber,,Helliwell
254
+ !Sample_contact_department = Biochemistry Department
255
+ !Sample_contact_institute = University of Otago
256
+ !Sample_contact_address = 710 Cumberland Road
257
+ !Sample_contact_city = Dunedin
258
+ !Sample_contact_zip/postal_code = 9016
259
+ !Sample_contact_country = New Zealand
260
+ !Sample_instrument_model = Illumina HiSeq 2500
261
+ !Sample_library_selection = Reduced Representation
262
+ !Sample_library_source = genomic
263
+ !Sample_library_strategy = Bisulfite-Seq
264
+ !Sample_relation = BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN15420268
265
+ !Sample_relation = SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX8651464
266
+ !Sample_supplementary_file_1 = ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649031/suppl/GSM4649031_Control5_CpG.txt.gz
267
+ !Sample_series_id = GSE153667
268
+ !Sample_data_row_count = 0
269
+ ^SAMPLE = GSM4649032
270
+ !Sample_title = Control6
271
+ !Sample_geo_accession = GSM4649032
272
+ !Sample_status = Public on Jul 02 2020
273
+ !Sample_submission_date = Jul 01 2020
274
+ !Sample_last_update_date = Jul 02 2020
275
+ !Sample_type = SRA
276
+ !Sample_channel_count = 1
277
+ !Sample_source_name_ch1 = Peripheral Blood Mononuclear Cells
278
+ !Sample_organism_ch1 = Homo sapiens
279
+ !Sample_taxid_ch1 = 9606
280
+ !Sample_characteristics_ch1 = disease state: Control
281
+ !Sample_molecule_ch1 = genomic DNA
282
+ !Sample_extract_protocol_ch1 = DNA was extracted from 200ul of PBMCs
283
+ !Sample_extract_protocol_ch1 = MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
284
+ !Sample_data_processing = reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
285
+ !Sample_data_processing = reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
286
+ !Sample_data_processing = bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
287
+ !Sample_data_processing = the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data
288
+ !Sample_data_processing = Genome_build: hg19
289
+ !Sample_data_processing = Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline.
290
+ !Sample_data_processing = Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). .
291
+ !Sample_platform_id = GPL16791
292
+ !Sample_contact_name = Amber,,Helliwell
293
+ !Sample_contact_department = Biochemistry Department
294
+ !Sample_contact_institute = University of Otago
295
+ !Sample_contact_address = 710 Cumberland Road
296
+ !Sample_contact_city = Dunedin
297
+ !Sample_contact_zip/postal_code = 9016
298
+ !Sample_contact_country = New Zealand
299
+ !Sample_instrument_model = Illumina HiSeq 2500
300
+ !Sample_library_selection = Reduced Representation
301
+ !Sample_library_source = genomic
302
+ !Sample_library_strategy = Bisulfite-Seq
303
+ !Sample_relation = BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN15420267
304
+ !Sample_relation = SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX8651465
305
+ !Sample_supplementary_file_1 = ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649032/suppl/GSM4649032_Control6_CpG.txt.gz
306
+ !Sample_series_id = GSE153667
307
+ !Sample_data_row_count = 0
308
+ ^SAMPLE = GSM4649033
309
+ !Sample_title = Control7
310
+ !Sample_geo_accession = GSM4649033
311
+ !Sample_status = Public on Jul 02 2020
312
+ !Sample_submission_date = Jul 01 2020
313
+ !Sample_last_update_date = Jul 02 2020
314
+ !Sample_type = SRA
315
+ !Sample_channel_count = 1
316
+ !Sample_source_name_ch1 = Peripheral Blood Mononuclear Cells
317
+ !Sample_organism_ch1 = Homo sapiens
318
+ !Sample_taxid_ch1 = 9606
319
+ !Sample_characteristics_ch1 = disease state: Control
320
+ !Sample_molecule_ch1 = genomic DNA
321
+ !Sample_extract_protocol_ch1 = DNA was extracted from 200ul of PBMCs
322
+ !Sample_extract_protocol_ch1 = MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
323
+ !Sample_data_processing = reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
324
+ !Sample_data_processing = reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
325
+ !Sample_data_processing = bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
326
+ !Sample_data_processing = the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data
327
+ !Sample_data_processing = Genome_build: hg19
328
+ !Sample_data_processing = Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline.
329
+ !Sample_data_processing = Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). .
330
+ !Sample_platform_id = GPL16791
331
+ !Sample_contact_name = Amber,,Helliwell
332
+ !Sample_contact_department = Biochemistry Department
333
+ !Sample_contact_institute = University of Otago
334
+ !Sample_contact_address = 710 Cumberland Road
335
+ !Sample_contact_city = Dunedin
336
+ !Sample_contact_zip/postal_code = 9016
337
+ !Sample_contact_country = New Zealand
338
+ !Sample_instrument_model = Illumina HiSeq 2500
339
+ !Sample_library_selection = Reduced Representation
340
+ !Sample_library_source = genomic
341
+ !Sample_library_strategy = Bisulfite-Seq
342
+ !Sample_relation = BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN15420266
343
+ !Sample_relation = SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX8651466
344
+ !Sample_supplementary_file_1 = ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649033/suppl/GSM4649033_Control7_CpG.txt.gz
345
+ !Sample_series_id = GSE153667
346
+ !Sample_data_row_count = 0
347
+ ^SAMPLE = GSM4649034
348
+ !Sample_title = Control8
349
+ !Sample_geo_accession = GSM4649034
350
+ !Sample_status = Public on Jul 02 2020
351
+ !Sample_submission_date = Jul 01 2020
352
+ !Sample_last_update_date = Jul 02 2020
353
+ !Sample_type = SRA
354
+ !Sample_channel_count = 1
355
+ !Sample_source_name_ch1 = Peripheral Blood Mononuclear Cells
356
+ !Sample_organism_ch1 = Homo sapiens
357
+ !Sample_taxid_ch1 = 9606
358
+ !Sample_characteristics_ch1 = disease state: Control
359
+ !Sample_molecule_ch1 = genomic DNA
360
+ !Sample_extract_protocol_ch1 = DNA was extracted from 200ul of PBMCs
361
+ !Sample_extract_protocol_ch1 = MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
362
+ !Sample_data_processing = reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
363
+ !Sample_data_processing = reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
364
+ !Sample_data_processing = bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
365
+ !Sample_data_processing = the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data
366
+ !Sample_data_processing = Genome_build: hg19
367
+ !Sample_data_processing = Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline.
368
+ !Sample_data_processing = Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). .
369
+ !Sample_platform_id = GPL16791
370
+ !Sample_contact_name = Amber,,Helliwell
371
+ !Sample_contact_department = Biochemistry Department
372
+ !Sample_contact_institute = University of Otago
373
+ !Sample_contact_address = 710 Cumberland Road
374
+ !Sample_contact_city = Dunedin
375
+ !Sample_contact_zip/postal_code = 9016
376
+ !Sample_contact_country = New Zealand
377
+ !Sample_instrument_model = Illumina HiSeq 2500
378
+ !Sample_library_selection = Reduced Representation
379
+ !Sample_library_source = genomic
380
+ !Sample_library_strategy = Bisulfite-Seq
381
+ !Sample_relation = BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN15420265
382
+ !Sample_relation = SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX8651467
383
+ !Sample_supplementary_file_1 = ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649034/suppl/GSM4649034_Control8_CpG.txt.gz
384
+ !Sample_series_id = GSE153667
385
+ !Sample_data_row_count = 0
386
+ ^SAMPLE = GSM4649035
387
+ !Sample_title = Control9
388
+ !Sample_geo_accession = GSM4649035
389
+ !Sample_status = Public on Jul 02 2020
390
+ !Sample_submission_date = Jul 01 2020
391
+ !Sample_last_update_date = Jul 02 2020
392
+ !Sample_type = SRA
393
+ !Sample_channel_count = 1
394
+ !Sample_source_name_ch1 = Peripheral Blood Mononuclear Cells
395
+ !Sample_organism_ch1 = Homo sapiens
396
+ !Sample_taxid_ch1 = 9606
397
+ !Sample_characteristics_ch1 = disease state: Control
398
+ !Sample_molecule_ch1 = genomic DNA
399
+ !Sample_extract_protocol_ch1 = DNA was extracted from 200ul of PBMCs
400
+ !Sample_extract_protocol_ch1 = MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
401
+ !Sample_data_processing = reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
402
+ !Sample_data_processing = reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
403
+ !Sample_data_processing = bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
404
+ !Sample_data_processing = the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data
405
+ !Sample_data_processing = Genome_build: hg19
406
+ !Sample_data_processing = Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline.
407
+ !Sample_data_processing = Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). .
408
+ !Sample_platform_id = GPL16791
409
+ !Sample_contact_name = Amber,,Helliwell
410
+ !Sample_contact_department = Biochemistry Department
411
+ !Sample_contact_institute = University of Otago
412
+ !Sample_contact_address = 710 Cumberland Road
413
+ !Sample_contact_city = Dunedin
414
+ !Sample_contact_zip/postal_code = 9016
415
+ !Sample_contact_country = New Zealand
416
+ !Sample_instrument_model = Illumina HiSeq 2500
417
+ !Sample_library_selection = Reduced Representation
418
+ !Sample_library_source = genomic
419
+ !Sample_library_strategy = Bisulfite-Seq
420
+ !Sample_relation = BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN15420264
421
+ !Sample_relation = SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX8651468
422
+ !Sample_supplementary_file_1 = ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649035/suppl/GSM4649035_Control9_CpG.txt.gz
423
+ !Sample_series_id = GSE153667
424
+ !Sample_data_row_count = 0
425
+ ^SAMPLE = GSM4649036
426
+ !Sample_title = Control10
427
+ !Sample_geo_accession = GSM4649036
428
+ !Sample_status = Public on Jul 02 2020
429
+ !Sample_submission_date = Jul 01 2020
430
+ !Sample_last_update_date = Jul 02 2020
431
+ !Sample_type = SRA
432
+ !Sample_channel_count = 1
433
+ !Sample_source_name_ch1 = Peripheral Blood Mononuclear Cells
434
+ !Sample_organism_ch1 = Homo sapiens
435
+ !Sample_taxid_ch1 = 9606
436
+ !Sample_characteristics_ch1 = disease state: Control
437
+ !Sample_molecule_ch1 = genomic DNA
438
+ !Sample_extract_protocol_ch1 = DNA was extracted from 200ul of PBMCs
439
+ !Sample_extract_protocol_ch1 = MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
440
+ !Sample_data_processing = reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
441
+ !Sample_data_processing = reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
442
+ !Sample_data_processing = bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
443
+ !Sample_data_processing = the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data
444
+ !Sample_data_processing = Genome_build: hg19
445
+ !Sample_data_processing = Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline.
446
+ !Sample_data_processing = Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). .
447
+ !Sample_platform_id = GPL16791
448
+ !Sample_contact_name = Amber,,Helliwell
449
+ !Sample_contact_department = Biochemistry Department
450
+ !Sample_contact_institute = University of Otago
451
+ !Sample_contact_address = 710 Cumberland Road
452
+ !Sample_contact_city = Dunedin
453
+ !Sample_contact_zip/postal_code = 9016
454
+ !Sample_contact_country = New Zealand
455
+ !Sample_instrument_model = Illumina HiSeq 2500
456
+ !Sample_library_selection = Reduced Representation
457
+ !Sample_library_source = genomic
458
+ !Sample_library_strategy = Bisulfite-Seq
459
+ !Sample_relation = BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN15420263
460
+ !Sample_relation = SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX8651469
461
+ !Sample_supplementary_file_1 = ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649036/suppl/GSM4649036_Control10_CpG.txt.gz
462
+ !Sample_series_id = GSE153667
463
+ !Sample_data_row_count = 0
464
+ ^SAMPLE = GSM4649037
465
+ !Sample_title = Patient1
466
+ !Sample_geo_accession = GSM4649037
467
+ !Sample_status = Public on Jul 02 2020
468
+ !Sample_submission_date = Jul 01 2020
469
+ !Sample_last_update_date = Jul 02 2020
470
+ !Sample_type = SRA
471
+ !Sample_channel_count = 1
472
+ !Sample_source_name_ch1 = Peripheral Blood Mononuclear Cells
473
+ !Sample_organism_ch1 = Homo sapiens
474
+ !Sample_taxid_ch1 = 9606
475
+ !Sample_characteristics_ch1 = disease state: Patient
476
+ !Sample_molecule_ch1 = genomic DNA
477
+ !Sample_extract_protocol_ch1 = DNA was extracted from 200ul of PBMCs
478
+ !Sample_extract_protocol_ch1 = MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
479
+ !Sample_data_processing = reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
480
+ !Sample_data_processing = reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
481
+ !Sample_data_processing = bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
482
+ !Sample_data_processing = the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data
483
+ !Sample_data_processing = Genome_build: hg19
484
+ !Sample_data_processing = Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline.
485
+ !Sample_data_processing = Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). .
486
+ !Sample_platform_id = GPL16791
487
+ !Sample_contact_name = Amber,,Helliwell
488
+ !Sample_contact_department = Biochemistry Department
489
+ !Sample_contact_institute = University of Otago
490
+ !Sample_contact_address = 710 Cumberland Road
491
+ !Sample_contact_city = Dunedin
492
+ !Sample_contact_zip/postal_code = 9016
493
+ !Sample_contact_country = New Zealand
494
+ !Sample_instrument_model = Illumina HiSeq 2500
495
+ !Sample_library_selection = Reduced Representation
496
+ !Sample_library_source = genomic
497
+ !Sample_library_strategy = Bisulfite-Seq
498
+ !Sample_relation = BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN15420262
499
+ !Sample_relation = SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX8651470
500
+ !Sample_supplementary_file_1 = ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649037/suppl/GSM4649037_Patient1_CpG.txt.gz
501
+ !Sample_series_id = GSE153667
502
+ !Sample_data_row_count = 0
503
+ ^SAMPLE = GSM4649038
504
+ !Sample_title = Patient2
505
+ !Sample_geo_accession = GSM4649038
506
+ !Sample_status = Public on Jul 02 2020
507
+ !Sample_submission_date = Jul 01 2020
508
+ !Sample_last_update_date = Jul 02 2020
509
+ !Sample_type = SRA
510
+ !Sample_channel_count = 1
511
+ !Sample_source_name_ch1 = Peripheral Blood Mononuclear Cells
512
+ !Sample_organism_ch1 = Homo sapiens
513
+ !Sample_taxid_ch1 = 9606
514
+ !Sample_characteristics_ch1 = disease state: Patient
515
+ !Sample_molecule_ch1 = genomic DNA
516
+ !Sample_extract_protocol_ch1 = DNA was extracted from 200ul of PBMCs
517
+ !Sample_extract_protocol_ch1 = MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
518
+ !Sample_data_processing = reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
519
+ !Sample_data_processing = reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
520
+ !Sample_data_processing = bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
521
+ !Sample_data_processing = the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data
522
+ !Sample_data_processing = Genome_build: hg19
523
+ !Sample_data_processing = Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline.
524
+ !Sample_data_processing = Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). .
525
+ !Sample_platform_id = GPL16791
526
+ !Sample_contact_name = Amber,,Helliwell
527
+ !Sample_contact_department = Biochemistry Department
528
+ !Sample_contact_institute = University of Otago
529
+ !Sample_contact_address = 710 Cumberland Road
530
+ !Sample_contact_city = Dunedin
531
+ !Sample_contact_zip/postal_code = 9016
532
+ !Sample_contact_country = New Zealand
533
+ !Sample_instrument_model = Illumina HiSeq 2500
534
+ !Sample_library_selection = Reduced Representation
535
+ !Sample_library_source = genomic
536
+ !Sample_library_strategy = Bisulfite-Seq
537
+ !Sample_relation = BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN15420261
538
+ !Sample_relation = SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX8651471
539
+ !Sample_supplementary_file_1 = ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649038/suppl/GSM4649038_Patient2_CpG.txt.gz
540
+ !Sample_series_id = GSE153667
541
+ !Sample_data_row_count = 0
542
+ ^SAMPLE = GSM4649039
543
+ !Sample_title = Patient3
544
+ !Sample_geo_accession = GSM4649039
545
+ !Sample_status = Public on Jul 02 2020
546
+ !Sample_submission_date = Jul 01 2020
547
+ !Sample_last_update_date = Jul 02 2020
548
+ !Sample_type = SRA
549
+ !Sample_channel_count = 1
550
+ !Sample_source_name_ch1 = Peripheral Blood Mononuclear Cells
551
+ !Sample_organism_ch1 = Homo sapiens
552
+ !Sample_taxid_ch1 = 9606
553
+ !Sample_characteristics_ch1 = disease state: Patient
554
+ !Sample_molecule_ch1 = genomic DNA
555
+ !Sample_extract_protocol_ch1 = DNA was extracted from 200ul of PBMCs
556
+ !Sample_extract_protocol_ch1 = MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
557
+ !Sample_data_processing = reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
558
+ !Sample_data_processing = reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
559
+ !Sample_data_processing = bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
560
+ !Sample_data_processing = the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data
561
+ !Sample_data_processing = Genome_build: hg19
562
+ !Sample_data_processing = Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline.
563
+ !Sample_data_processing = Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). .
564
+ !Sample_platform_id = GPL16791
565
+ !Sample_contact_name = Amber,,Helliwell
566
+ !Sample_contact_department = Biochemistry Department
567
+ !Sample_contact_institute = University of Otago
568
+ !Sample_contact_address = 710 Cumberland Road
569
+ !Sample_contact_city = Dunedin
570
+ !Sample_contact_zip/postal_code = 9016
571
+ !Sample_contact_country = New Zealand
572
+ !Sample_instrument_model = Illumina HiSeq 2500
573
+ !Sample_library_selection = Reduced Representation
574
+ !Sample_library_source = genomic
575
+ !Sample_library_strategy = Bisulfite-Seq
576
+ !Sample_relation = BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN15420260
577
+ !Sample_relation = SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX8651472
578
+ !Sample_supplementary_file_1 = ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649039/suppl/GSM4649039_Patient3_CpG.txt.gz
579
+ !Sample_series_id = GSE153667
580
+ !Sample_data_row_count = 0
581
+ ^SAMPLE = GSM4649040
582
+ !Sample_title = Patient4
583
+ !Sample_geo_accession = GSM4649040
584
+ !Sample_status = Public on Jul 02 2020
585
+ !Sample_submission_date = Jul 01 2020
586
+ !Sample_last_update_date = Jul 02 2020
587
+ !Sample_type = SRA
588
+ !Sample_channel_count = 1
589
+ !Sample_source_name_ch1 = Peripheral Blood Mononuclear Cells
590
+ !Sample_organism_ch1 = Homo sapiens
591
+ !Sample_taxid_ch1 = 9606
592
+ !Sample_characteristics_ch1 = disease state: Patient
593
+ !Sample_molecule_ch1 = genomic DNA
594
+ !Sample_extract_protocol_ch1 = DNA was extracted from 200ul of PBMCs
595
+ !Sample_extract_protocol_ch1 = MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
596
+ !Sample_data_processing = reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
597
+ !Sample_data_processing = reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
598
+ !Sample_data_processing = bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
599
+ !Sample_data_processing = the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data
600
+ !Sample_data_processing = Genome_build: hg19
601
+ !Sample_data_processing = Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline.
602
+ !Sample_data_processing = Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). .
603
+ !Sample_platform_id = GPL16791
604
+ !Sample_contact_name = Amber,,Helliwell
605
+ !Sample_contact_department = Biochemistry Department
606
+ !Sample_contact_institute = University of Otago
607
+ !Sample_contact_address = 710 Cumberland Road
608
+ !Sample_contact_city = Dunedin
609
+ !Sample_contact_zip/postal_code = 9016
610
+ !Sample_contact_country = New Zealand
611
+ !Sample_instrument_model = Illumina HiSeq 2500
612
+ !Sample_library_selection = Reduced Representation
613
+ !Sample_library_source = genomic
614
+ !Sample_library_strategy = Bisulfite-Seq
615
+ !Sample_relation = BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN15420259
616
+ !Sample_relation = SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX8651473
617
+ !Sample_supplementary_file_1 = ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649040/suppl/GSM4649040_Patient4_CpG.txt.gz
618
+ !Sample_series_id = GSE153667
619
+ !Sample_data_row_count = 0
620
+ ^SAMPLE = GSM4649041
621
+ !Sample_title = Patient5
622
+ !Sample_geo_accession = GSM4649041
623
+ !Sample_status = Public on Jul 02 2020
624
+ !Sample_submission_date = Jul 01 2020
625
+ !Sample_last_update_date = Jul 02 2020
626
+ !Sample_type = SRA
627
+ !Sample_channel_count = 1
628
+ !Sample_source_name_ch1 = Peripheral Blood Mononuclear Cells
629
+ !Sample_organism_ch1 = Homo sapiens
630
+ !Sample_taxid_ch1 = 9606
631
+ !Sample_characteristics_ch1 = disease state: Patient
632
+ !Sample_molecule_ch1 = genomic DNA
633
+ !Sample_extract_protocol_ch1 = DNA was extracted from 200ul of PBMCs
634
+ !Sample_extract_protocol_ch1 = MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
635
+ !Sample_data_processing = reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
636
+ !Sample_data_processing = reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
637
+ !Sample_data_processing = bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
638
+ !Sample_data_processing = the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data
639
+ !Sample_data_processing = Genome_build: hg19
640
+ !Sample_data_processing = Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline.
641
+ !Sample_data_processing = Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). .
642
+ !Sample_platform_id = GPL16791
643
+ !Sample_contact_name = Amber,,Helliwell
644
+ !Sample_contact_department = Biochemistry Department
645
+ !Sample_contact_institute = University of Otago
646
+ !Sample_contact_address = 710 Cumberland Road
647
+ !Sample_contact_city = Dunedin
648
+ !Sample_contact_zip/postal_code = 9016
649
+ !Sample_contact_country = New Zealand
650
+ !Sample_instrument_model = Illumina HiSeq 2500
651
+ !Sample_library_selection = Reduced Representation
652
+ !Sample_library_source = genomic
653
+ !Sample_library_strategy = Bisulfite-Seq
654
+ !Sample_relation = BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN15420258
655
+ !Sample_relation = SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX8651474
656
+ !Sample_supplementary_file_1 = ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649041/suppl/GSM4649041_Patient5_CpG.txt.gz
657
+ !Sample_series_id = GSE153667
658
+ !Sample_data_row_count = 0
659
+ ^SAMPLE = GSM4649042
660
+ !Sample_title = Patient6
661
+ !Sample_geo_accession = GSM4649042
662
+ !Sample_status = Public on Jul 02 2020
663
+ !Sample_submission_date = Jul 01 2020
664
+ !Sample_last_update_date = Jul 02 2020
665
+ !Sample_type = SRA
666
+ !Sample_channel_count = 1
667
+ !Sample_source_name_ch1 = Peripheral Blood Mononuclear Cells
668
+ !Sample_organism_ch1 = Homo sapiens
669
+ !Sample_taxid_ch1 = 9606
670
+ !Sample_characteristics_ch1 = disease state: Patient
671
+ !Sample_molecule_ch1 = genomic DNA
672
+ !Sample_extract_protocol_ch1 = DNA was extracted from 200ul of PBMCs
673
+ !Sample_extract_protocol_ch1 = MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
674
+ !Sample_data_processing = reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
675
+ !Sample_data_processing = reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
676
+ !Sample_data_processing = bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
677
+ !Sample_data_processing = the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data
678
+ !Sample_data_processing = Genome_build: hg19
679
+ !Sample_data_processing = Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline.
680
+ !Sample_data_processing = Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). .
681
+ !Sample_platform_id = GPL16791
682
+ !Sample_contact_name = Amber,,Helliwell
683
+ !Sample_contact_department = Biochemistry Department
684
+ !Sample_contact_institute = University of Otago
685
+ !Sample_contact_address = 710 Cumberland Road
686
+ !Sample_contact_city = Dunedin
687
+ !Sample_contact_zip/postal_code = 9016
688
+ !Sample_contact_country = New Zealand
689
+ !Sample_instrument_model = Illumina HiSeq 2500
690
+ !Sample_library_selection = Reduced Representation
691
+ !Sample_library_source = genomic
692
+ !Sample_library_strategy = Bisulfite-Seq
693
+ !Sample_relation = BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN15420257
694
+ !Sample_relation = SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX8651475
695
+ !Sample_supplementary_file_1 = ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649042/suppl/GSM4649042_Patient6_CpG.txt.gz
696
+ !Sample_series_id = GSE153667
697
+ !Sample_data_row_count = 0
698
+ ^SAMPLE = GSM4649043
699
+ !Sample_title = Patient7
700
+ !Sample_geo_accession = GSM4649043
701
+ !Sample_status = Public on Jul 02 2020
702
+ !Sample_submission_date = Jul 01 2020
703
+ !Sample_last_update_date = Jul 02 2020
704
+ !Sample_type = SRA
705
+ !Sample_channel_count = 1
706
+ !Sample_source_name_ch1 = Peripheral Blood Mononuclear Cells
707
+ !Sample_organism_ch1 = Homo sapiens
708
+ !Sample_taxid_ch1 = 9606
709
+ !Sample_characteristics_ch1 = disease state: Patient
710
+ !Sample_molecule_ch1 = genomic DNA
711
+ !Sample_extract_protocol_ch1 = DNA was extracted from 200ul of PBMCs
712
+ !Sample_extract_protocol_ch1 = MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
713
+ !Sample_data_processing = reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
714
+ !Sample_data_processing = reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
715
+ !Sample_data_processing = bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
716
+ !Sample_data_processing = the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data
717
+ !Sample_data_processing = Genome_build: hg19
718
+ !Sample_data_processing = Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline.
719
+ !Sample_data_processing = Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). .
720
+ !Sample_platform_id = GPL16791
721
+ !Sample_contact_name = Amber,,Helliwell
722
+ !Sample_contact_department = Biochemistry Department
723
+ !Sample_contact_institute = University of Otago
724
+ !Sample_contact_address = 710 Cumberland Road
725
+ !Sample_contact_city = Dunedin
726
+ !Sample_contact_zip/postal_code = 9016
727
+ !Sample_contact_country = New Zealand
728
+ !Sample_instrument_model = Illumina HiSeq 2500
729
+ !Sample_library_selection = Reduced Representation
730
+ !Sample_library_source = genomic
731
+ !Sample_library_strategy = Bisulfite-Seq
732
+ !Sample_relation = BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN15420256
733
+ !Sample_relation = SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX8651476
734
+ !Sample_supplementary_file_1 = ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649043/suppl/GSM4649043_Patient7_CpG.txt.gz
735
+ !Sample_series_id = GSE153667
736
+ !Sample_data_row_count = 0
737
+ ^SAMPLE = GSM4649044
738
+ !Sample_title = Patient8
739
+ !Sample_geo_accession = GSM4649044
740
+ !Sample_status = Public on Jul 02 2020
741
+ !Sample_submission_date = Jul 01 2020
742
+ !Sample_last_update_date = Jul 02 2020
743
+ !Sample_type = SRA
744
+ !Sample_channel_count = 1
745
+ !Sample_source_name_ch1 = Peripheral Blood Mononuclear Cells
746
+ !Sample_organism_ch1 = Homo sapiens
747
+ !Sample_taxid_ch1 = 9606
748
+ !Sample_characteristics_ch1 = disease state: Patient
749
+ !Sample_molecule_ch1 = genomic DNA
750
+ !Sample_extract_protocol_ch1 = DNA was extracted from 200ul of PBMCs
751
+ !Sample_extract_protocol_ch1 = MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
752
+ !Sample_data_processing = reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
753
+ !Sample_data_processing = reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
754
+ !Sample_data_processing = bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
755
+ !Sample_data_processing = the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data
756
+ !Sample_data_processing = Genome_build: hg19
757
+ !Sample_data_processing = Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline.
758
+ !Sample_data_processing = Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). .
759
+ !Sample_platform_id = GPL16791
760
+ !Sample_contact_name = Amber,,Helliwell
761
+ !Sample_contact_department = Biochemistry Department
762
+ !Sample_contact_institute = University of Otago
763
+ !Sample_contact_address = 710 Cumberland Road
764
+ !Sample_contact_city = Dunedin
765
+ !Sample_contact_zip/postal_code = 9016
766
+ !Sample_contact_country = New Zealand
767
+ !Sample_instrument_model = Illumina HiSeq 2500
768
+ !Sample_library_selection = Reduced Representation
769
+ !Sample_library_source = genomic
770
+ !Sample_library_strategy = Bisulfite-Seq
771
+ !Sample_relation = BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN15420255
772
+ !Sample_relation = SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX8651477
773
+ !Sample_supplementary_file_1 = ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649044/suppl/GSM4649044_Patient8_CpG.txt.gz
774
+ !Sample_series_id = GSE153667
775
+ !Sample_data_row_count = 0
776
+ ^SAMPLE = GSM4649045
777
+ !Sample_title = Patient9
778
+ !Sample_geo_accession = GSM4649045
779
+ !Sample_status = Public on Jul 02 2020
780
+ !Sample_submission_date = Jul 01 2020
781
+ !Sample_last_update_date = Jul 02 2020
782
+ !Sample_type = SRA
783
+ !Sample_channel_count = 1
784
+ !Sample_source_name_ch1 = Peripheral Blood Mononuclear Cells
785
+ !Sample_organism_ch1 = Homo sapiens
786
+ !Sample_taxid_ch1 = 9606
787
+ !Sample_characteristics_ch1 = disease state: Patient
788
+ !Sample_molecule_ch1 = genomic DNA
789
+ !Sample_extract_protocol_ch1 = DNA was extracted from 200ul of PBMCs
790
+ !Sample_extract_protocol_ch1 = MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
791
+ !Sample_data_processing = reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
792
+ !Sample_data_processing = reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
793
+ !Sample_data_processing = bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
794
+ !Sample_data_processing = the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data
795
+ !Sample_data_processing = Genome_build: hg19
796
+ !Sample_data_processing = Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline.
797
+ !Sample_data_processing = Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). .
798
+ !Sample_platform_id = GPL16791
799
+ !Sample_contact_name = Amber,,Helliwell
800
+ !Sample_contact_department = Biochemistry Department
801
+ !Sample_contact_institute = University of Otago
802
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238
+ the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data
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+ <Status database="GEO">
260
+ <Submission-Date>2020-07-01</Submission-Date>
261
+ <Release-Date>2020-07-02</Release-Date>
262
+ <Last-Update-Date>2020-07-02</Last-Update-Date>
263
+ </Status>
264
+ <Title>Control5</Title>
265
+ <Accession database="GEO">GSM4649031</Accession>
266
+ <Type>SRA</Type>
267
+ <Channel-Count>1</Channel-Count>
268
+ <Channel position="1">
269
+ <Source>Peripheral Blood Mononuclear Cells</Source>
270
+ <Organism taxid="9606">Homo sapiens</Organism>
271
+ <Characteristics tag="disease state">
272
+ Control
273
+ </Characteristics>
274
+ <Molecule>genomic DNA</Molecule>
275
+ <Extract-Protocol>
276
+ DNA was extracted from 200ul of PBMCs
277
+ MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
278
+ </Extract-Protocol>
279
+ </Channel>
280
+ <Data-Processing>
281
+ reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
282
+ reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
283
+ bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
284
+ the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data
285
+ Genome_build: hg19
286
+ Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline.
287
+ Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). .
288
+ </Data-Processing>
289
+ <Platform-Ref ref="GPL16791" />
290
+ <Library-Strategy>Bisulfite-Seq</Library-Strategy>
291
+ <Library-Source>genomic</Library-Source>
292
+ <Library-Selection>Reduced Representation</Library-Selection>
293
+ <Instrument-Model>
294
+ <Predefined>Illumina HiSeq 2500</Predefined>
295
+ </Instrument-Model>
296
+ <Contact-Ref ref="contrib1" />
297
+ <Supplementary-Data type="TXT">
298
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649031/suppl/GSM4649031_Control5_CpG.txt.gz
299
+ </Supplementary-Data>
300
+ <Relation type="BioSample" target="https://www.ncbi.nlm.nih.gov/biosample/SAMN15420268" />
301
+ <Relation type="SRA" target="https://www.ncbi.nlm.nih.gov/sra?term=SRX8651464" />
302
+ </Sample>
303
+
304
+ <Sample iid="GSM4649032">
305
+ <Status database="GEO">
306
+ <Submission-Date>2020-07-01</Submission-Date>
307
+ <Release-Date>2020-07-02</Release-Date>
308
+ <Last-Update-Date>2020-07-02</Last-Update-Date>
309
+ </Status>
310
+ <Title>Control6</Title>
311
+ <Accession database="GEO">GSM4649032</Accession>
312
+ <Type>SRA</Type>
313
+ <Channel-Count>1</Channel-Count>
314
+ <Channel position="1">
315
+ <Source>Peripheral Blood Mononuclear Cells</Source>
316
+ <Organism taxid="9606">Homo sapiens</Organism>
317
+ <Characteristics tag="disease state">
318
+ Control
319
+ </Characteristics>
320
+ <Molecule>genomic DNA</Molecule>
321
+ <Extract-Protocol>
322
+ DNA was extracted from 200ul of PBMCs
323
+ MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
324
+ </Extract-Protocol>
325
+ </Channel>
326
+ <Data-Processing>
327
+ reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
328
+ reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
329
+ bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
330
+ the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data
331
+ Genome_build: hg19
332
+ Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline.
333
+ Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). .
334
+ </Data-Processing>
335
+ <Platform-Ref ref="GPL16791" />
336
+ <Library-Strategy>Bisulfite-Seq</Library-Strategy>
337
+ <Library-Source>genomic</Library-Source>
338
+ <Library-Selection>Reduced Representation</Library-Selection>
339
+ <Instrument-Model>
340
+ <Predefined>Illumina HiSeq 2500</Predefined>
341
+ </Instrument-Model>
342
+ <Contact-Ref ref="contrib1" />
343
+ <Supplementary-Data type="TXT">
344
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649032/suppl/GSM4649032_Control6_CpG.txt.gz
345
+ </Supplementary-Data>
346
+ <Relation type="BioSample" target="https://www.ncbi.nlm.nih.gov/biosample/SAMN15420267" />
347
+ <Relation type="SRA" target="https://www.ncbi.nlm.nih.gov/sra?term=SRX8651465" />
348
+ </Sample>
349
+
350
+ <Sample iid="GSM4649033">
351
+ <Status database="GEO">
352
+ <Submission-Date>2020-07-01</Submission-Date>
353
+ <Release-Date>2020-07-02</Release-Date>
354
+ <Last-Update-Date>2020-07-02</Last-Update-Date>
355
+ </Status>
356
+ <Title>Control7</Title>
357
+ <Accession database="GEO">GSM4649033</Accession>
358
+ <Type>SRA</Type>
359
+ <Channel-Count>1</Channel-Count>
360
+ <Channel position="1">
361
+ <Source>Peripheral Blood Mononuclear Cells</Source>
362
+ <Organism taxid="9606">Homo sapiens</Organism>
363
+ <Characteristics tag="disease state">
364
+ Control
365
+ </Characteristics>
366
+ <Molecule>genomic DNA</Molecule>
367
+ <Extract-Protocol>
368
+ DNA was extracted from 200ul of PBMCs
369
+ MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
370
+ </Extract-Protocol>
371
+ </Channel>
372
+ <Data-Processing>
373
+ reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
374
+ reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
375
+ bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
376
+ the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data
377
+ Genome_build: hg19
378
+ Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline.
379
+ Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). .
380
+ </Data-Processing>
381
+ <Platform-Ref ref="GPL16791" />
382
+ <Library-Strategy>Bisulfite-Seq</Library-Strategy>
383
+ <Library-Source>genomic</Library-Source>
384
+ <Library-Selection>Reduced Representation</Library-Selection>
385
+ <Instrument-Model>
386
+ <Predefined>Illumina HiSeq 2500</Predefined>
387
+ </Instrument-Model>
388
+ <Contact-Ref ref="contrib1" />
389
+ <Supplementary-Data type="TXT">
390
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649033/suppl/GSM4649033_Control7_CpG.txt.gz
391
+ </Supplementary-Data>
392
+ <Relation type="BioSample" target="https://www.ncbi.nlm.nih.gov/biosample/SAMN15420266" />
393
+ <Relation type="SRA" target="https://www.ncbi.nlm.nih.gov/sra?term=SRX8651466" />
394
+ </Sample>
395
+
396
+ <Sample iid="GSM4649034">
397
+ <Status database="GEO">
398
+ <Submission-Date>2020-07-01</Submission-Date>
399
+ <Release-Date>2020-07-02</Release-Date>
400
+ <Last-Update-Date>2020-07-02</Last-Update-Date>
401
+ </Status>
402
+ <Title>Control8</Title>
403
+ <Accession database="GEO">GSM4649034</Accession>
404
+ <Type>SRA</Type>
405
+ <Channel-Count>1</Channel-Count>
406
+ <Channel position="1">
407
+ <Source>Peripheral Blood Mononuclear Cells</Source>
408
+ <Organism taxid="9606">Homo sapiens</Organism>
409
+ <Characteristics tag="disease state">
410
+ Control
411
+ </Characteristics>
412
+ <Molecule>genomic DNA</Molecule>
413
+ <Extract-Protocol>
414
+ DNA was extracted from 200ul of PBMCs
415
+ MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
416
+ </Extract-Protocol>
417
+ </Channel>
418
+ <Data-Processing>
419
+ reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
420
+ reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
421
+ bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
422
+ the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data
423
+ Genome_build: hg19
424
+ Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline.
425
+ Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). .
426
+ </Data-Processing>
427
+ <Platform-Ref ref="GPL16791" />
428
+ <Library-Strategy>Bisulfite-Seq</Library-Strategy>
429
+ <Library-Source>genomic</Library-Source>
430
+ <Library-Selection>Reduced Representation</Library-Selection>
431
+ <Instrument-Model>
432
+ <Predefined>Illumina HiSeq 2500</Predefined>
433
+ </Instrument-Model>
434
+ <Contact-Ref ref="contrib1" />
435
+ <Supplementary-Data type="TXT">
436
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649034/suppl/GSM4649034_Control8_CpG.txt.gz
437
+ </Supplementary-Data>
438
+ <Relation type="BioSample" target="https://www.ncbi.nlm.nih.gov/biosample/SAMN15420265" />
439
+ <Relation type="SRA" target="https://www.ncbi.nlm.nih.gov/sra?term=SRX8651467" />
440
+ </Sample>
441
+
442
+ <Sample iid="GSM4649035">
443
+ <Status database="GEO">
444
+ <Submission-Date>2020-07-01</Submission-Date>
445
+ <Release-Date>2020-07-02</Release-Date>
446
+ <Last-Update-Date>2020-07-02</Last-Update-Date>
447
+ </Status>
448
+ <Title>Control9</Title>
449
+ <Accession database="GEO">GSM4649035</Accession>
450
+ <Type>SRA</Type>
451
+ <Channel-Count>1</Channel-Count>
452
+ <Channel position="1">
453
+ <Source>Peripheral Blood Mononuclear Cells</Source>
454
+ <Organism taxid="9606">Homo sapiens</Organism>
455
+ <Characteristics tag="disease state">
456
+ Control
457
+ </Characteristics>
458
+ <Molecule>genomic DNA</Molecule>
459
+ <Extract-Protocol>
460
+ DNA was extracted from 200ul of PBMCs
461
+ MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
462
+ </Extract-Protocol>
463
+ </Channel>
464
+ <Data-Processing>
465
+ reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
466
+ reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
467
+ bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
468
+ the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data
469
+ Genome_build: hg19
470
+ Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline.
471
+ Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). .
472
+ </Data-Processing>
473
+ <Platform-Ref ref="GPL16791" />
474
+ <Library-Strategy>Bisulfite-Seq</Library-Strategy>
475
+ <Library-Source>genomic</Library-Source>
476
+ <Library-Selection>Reduced Representation</Library-Selection>
477
+ <Instrument-Model>
478
+ <Predefined>Illumina HiSeq 2500</Predefined>
479
+ </Instrument-Model>
480
+ <Contact-Ref ref="contrib1" />
481
+ <Supplementary-Data type="TXT">
482
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649035/suppl/GSM4649035_Control9_CpG.txt.gz
483
+ </Supplementary-Data>
484
+ <Relation type="BioSample" target="https://www.ncbi.nlm.nih.gov/biosample/SAMN15420264" />
485
+ <Relation type="SRA" target="https://www.ncbi.nlm.nih.gov/sra?term=SRX8651468" />
486
+ </Sample>
487
+
488
+ <Sample iid="GSM4649036">
489
+ <Status database="GEO">
490
+ <Submission-Date>2020-07-01</Submission-Date>
491
+ <Release-Date>2020-07-02</Release-Date>
492
+ <Last-Update-Date>2020-07-02</Last-Update-Date>
493
+ </Status>
494
+ <Title>Control10</Title>
495
+ <Accession database="GEO">GSM4649036</Accession>
496
+ <Type>SRA</Type>
497
+ <Channel-Count>1</Channel-Count>
498
+ <Channel position="1">
499
+ <Source>Peripheral Blood Mononuclear Cells</Source>
500
+ <Organism taxid="9606">Homo sapiens</Organism>
501
+ <Characteristics tag="disease state">
502
+ Control
503
+ </Characteristics>
504
+ <Molecule>genomic DNA</Molecule>
505
+ <Extract-Protocol>
506
+ DNA was extracted from 200ul of PBMCs
507
+ MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
508
+ </Extract-Protocol>
509
+ </Channel>
510
+ <Data-Processing>
511
+ reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
512
+ reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
513
+ bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
514
+ the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data
515
+ Genome_build: hg19
516
+ Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline.
517
+ Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). .
518
+ </Data-Processing>
519
+ <Platform-Ref ref="GPL16791" />
520
+ <Library-Strategy>Bisulfite-Seq</Library-Strategy>
521
+ <Library-Source>genomic</Library-Source>
522
+ <Library-Selection>Reduced Representation</Library-Selection>
523
+ <Instrument-Model>
524
+ <Predefined>Illumina HiSeq 2500</Predefined>
525
+ </Instrument-Model>
526
+ <Contact-Ref ref="contrib1" />
527
+ <Supplementary-Data type="TXT">
528
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649036/suppl/GSM4649036_Control10_CpG.txt.gz
529
+ </Supplementary-Data>
530
+ <Relation type="BioSample" target="https://www.ncbi.nlm.nih.gov/biosample/SAMN15420263" />
531
+ <Relation type="SRA" target="https://www.ncbi.nlm.nih.gov/sra?term=SRX8651469" />
532
+ </Sample>
533
+
534
+ <Sample iid="GSM4649037">
535
+ <Status database="GEO">
536
+ <Submission-Date>2020-07-01</Submission-Date>
537
+ <Release-Date>2020-07-02</Release-Date>
538
+ <Last-Update-Date>2020-07-02</Last-Update-Date>
539
+ </Status>
540
+ <Title>Patient1</Title>
541
+ <Accession database="GEO">GSM4649037</Accession>
542
+ <Type>SRA</Type>
543
+ <Channel-Count>1</Channel-Count>
544
+ <Channel position="1">
545
+ <Source>Peripheral Blood Mononuclear Cells</Source>
546
+ <Organism taxid="9606">Homo sapiens</Organism>
547
+ <Characteristics tag="disease state">
548
+ Patient
549
+ </Characteristics>
550
+ <Molecule>genomic DNA</Molecule>
551
+ <Extract-Protocol>
552
+ DNA was extracted from 200ul of PBMCs
553
+ MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
554
+ </Extract-Protocol>
555
+ </Channel>
556
+ <Data-Processing>
557
+ reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
558
+ reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
559
+ bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
560
+ the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data
561
+ Genome_build: hg19
562
+ Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline.
563
+ Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). .
564
+ </Data-Processing>
565
+ <Platform-Ref ref="GPL16791" />
566
+ <Library-Strategy>Bisulfite-Seq</Library-Strategy>
567
+ <Library-Source>genomic</Library-Source>
568
+ <Library-Selection>Reduced Representation</Library-Selection>
569
+ <Instrument-Model>
570
+ <Predefined>Illumina HiSeq 2500</Predefined>
571
+ </Instrument-Model>
572
+ <Contact-Ref ref="contrib1" />
573
+ <Supplementary-Data type="TXT">
574
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649037/suppl/GSM4649037_Patient1_CpG.txt.gz
575
+ </Supplementary-Data>
576
+ <Relation type="BioSample" target="https://www.ncbi.nlm.nih.gov/biosample/SAMN15420262" />
577
+ <Relation type="SRA" target="https://www.ncbi.nlm.nih.gov/sra?term=SRX8651470" />
578
+ </Sample>
579
+
580
+ <Sample iid="GSM4649038">
581
+ <Status database="GEO">
582
+ <Submission-Date>2020-07-01</Submission-Date>
583
+ <Release-Date>2020-07-02</Release-Date>
584
+ <Last-Update-Date>2020-07-02</Last-Update-Date>
585
+ </Status>
586
+ <Title>Patient2</Title>
587
+ <Accession database="GEO">GSM4649038</Accession>
588
+ <Type>SRA</Type>
589
+ <Channel-Count>1</Channel-Count>
590
+ <Channel position="1">
591
+ <Source>Peripheral Blood Mononuclear Cells</Source>
592
+ <Organism taxid="9606">Homo sapiens</Organism>
593
+ <Characteristics tag="disease state">
594
+ Patient
595
+ </Characteristics>
596
+ <Molecule>genomic DNA</Molecule>
597
+ <Extract-Protocol>
598
+ DNA was extracted from 200ul of PBMCs
599
+ MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
600
+ </Extract-Protocol>
601
+ </Channel>
602
+ <Data-Processing>
603
+ reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
604
+ reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
605
+ bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
606
+ the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data
607
+ Genome_build: hg19
608
+ Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline.
609
+ Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). .
610
+ </Data-Processing>
611
+ <Platform-Ref ref="GPL16791" />
612
+ <Library-Strategy>Bisulfite-Seq</Library-Strategy>
613
+ <Library-Source>genomic</Library-Source>
614
+ <Library-Selection>Reduced Representation</Library-Selection>
615
+ <Instrument-Model>
616
+ <Predefined>Illumina HiSeq 2500</Predefined>
617
+ </Instrument-Model>
618
+ <Contact-Ref ref="contrib1" />
619
+ <Supplementary-Data type="TXT">
620
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649038/suppl/GSM4649038_Patient2_CpG.txt.gz
621
+ </Supplementary-Data>
622
+ <Relation type="BioSample" target="https://www.ncbi.nlm.nih.gov/biosample/SAMN15420261" />
623
+ <Relation type="SRA" target="https://www.ncbi.nlm.nih.gov/sra?term=SRX8651471" />
624
+ </Sample>
625
+
626
+ <Sample iid="GSM4649039">
627
+ <Status database="GEO">
628
+ <Submission-Date>2020-07-01</Submission-Date>
629
+ <Release-Date>2020-07-02</Release-Date>
630
+ <Last-Update-Date>2020-07-02</Last-Update-Date>
631
+ </Status>
632
+ <Title>Patient3</Title>
633
+ <Accession database="GEO">GSM4649039</Accession>
634
+ <Type>SRA</Type>
635
+ <Channel-Count>1</Channel-Count>
636
+ <Channel position="1">
637
+ <Source>Peripheral Blood Mononuclear Cells</Source>
638
+ <Organism taxid="9606">Homo sapiens</Organism>
639
+ <Characteristics tag="disease state">
640
+ Patient
641
+ </Characteristics>
642
+ <Molecule>genomic DNA</Molecule>
643
+ <Extract-Protocol>
644
+ DNA was extracted from 200ul of PBMCs
645
+ MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
646
+ </Extract-Protocol>
647
+ </Channel>
648
+ <Data-Processing>
649
+ reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
650
+ reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
651
+ bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
652
+ the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data
653
+ Genome_build: hg19
654
+ Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline.
655
+ Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). .
656
+ </Data-Processing>
657
+ <Platform-Ref ref="GPL16791" />
658
+ <Library-Strategy>Bisulfite-Seq</Library-Strategy>
659
+ <Library-Source>genomic</Library-Source>
660
+ <Library-Selection>Reduced Representation</Library-Selection>
661
+ <Instrument-Model>
662
+ <Predefined>Illumina HiSeq 2500</Predefined>
663
+ </Instrument-Model>
664
+ <Contact-Ref ref="contrib1" />
665
+ <Supplementary-Data type="TXT">
666
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649039/suppl/GSM4649039_Patient3_CpG.txt.gz
667
+ </Supplementary-Data>
668
+ <Relation type="BioSample" target="https://www.ncbi.nlm.nih.gov/biosample/SAMN15420260" />
669
+ <Relation type="SRA" target="https://www.ncbi.nlm.nih.gov/sra?term=SRX8651472" />
670
+ </Sample>
671
+
672
+ <Sample iid="GSM4649040">
673
+ <Status database="GEO">
674
+ <Submission-Date>2020-07-01</Submission-Date>
675
+ <Release-Date>2020-07-02</Release-Date>
676
+ <Last-Update-Date>2020-07-02</Last-Update-Date>
677
+ </Status>
678
+ <Title>Patient4</Title>
679
+ <Accession database="GEO">GSM4649040</Accession>
680
+ <Type>SRA</Type>
681
+ <Channel-Count>1</Channel-Count>
682
+ <Channel position="1">
683
+ <Source>Peripheral Blood Mononuclear Cells</Source>
684
+ <Organism taxid="9606">Homo sapiens</Organism>
685
+ <Characteristics tag="disease state">
686
+ Patient
687
+ </Characteristics>
688
+ <Molecule>genomic DNA</Molecule>
689
+ <Extract-Protocol>
690
+ DNA was extracted from 200ul of PBMCs
691
+ MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
692
+ </Extract-Protocol>
693
+ </Channel>
694
+ <Data-Processing>
695
+ reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
696
+ reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
697
+ bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
698
+ the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data
699
+ Genome_build: hg19
700
+ Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline.
701
+ Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). .
702
+ </Data-Processing>
703
+ <Platform-Ref ref="GPL16791" />
704
+ <Library-Strategy>Bisulfite-Seq</Library-Strategy>
705
+ <Library-Source>genomic</Library-Source>
706
+ <Library-Selection>Reduced Representation</Library-Selection>
707
+ <Instrument-Model>
708
+ <Predefined>Illumina HiSeq 2500</Predefined>
709
+ </Instrument-Model>
710
+ <Contact-Ref ref="contrib1" />
711
+ <Supplementary-Data type="TXT">
712
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649040/suppl/GSM4649040_Patient4_CpG.txt.gz
713
+ </Supplementary-Data>
714
+ <Relation type="BioSample" target="https://www.ncbi.nlm.nih.gov/biosample/SAMN15420259" />
715
+ <Relation type="SRA" target="https://www.ncbi.nlm.nih.gov/sra?term=SRX8651473" />
716
+ </Sample>
717
+
718
+ <Sample iid="GSM4649041">
719
+ <Status database="GEO">
720
+ <Submission-Date>2020-07-01</Submission-Date>
721
+ <Release-Date>2020-07-02</Release-Date>
722
+ <Last-Update-Date>2020-07-02</Last-Update-Date>
723
+ </Status>
724
+ <Title>Patient5</Title>
725
+ <Accession database="GEO">GSM4649041</Accession>
726
+ <Type>SRA</Type>
727
+ <Channel-Count>1</Channel-Count>
728
+ <Channel position="1">
729
+ <Source>Peripheral Blood Mononuclear Cells</Source>
730
+ <Organism taxid="9606">Homo sapiens</Organism>
731
+ <Characteristics tag="disease state">
732
+ Patient
733
+ </Characteristics>
734
+ <Molecule>genomic DNA</Molecule>
735
+ <Extract-Protocol>
736
+ DNA was extracted from 200ul of PBMCs
737
+ MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
738
+ </Extract-Protocol>
739
+ </Channel>
740
+ <Data-Processing>
741
+ reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
742
+ reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
743
+ bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
744
+ the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data
745
+ Genome_build: hg19
746
+ Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline.
747
+ Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). .
748
+ </Data-Processing>
749
+ <Platform-Ref ref="GPL16791" />
750
+ <Library-Strategy>Bisulfite-Seq</Library-Strategy>
751
+ <Library-Source>genomic</Library-Source>
752
+ <Library-Selection>Reduced Representation</Library-Selection>
753
+ <Instrument-Model>
754
+ <Predefined>Illumina HiSeq 2500</Predefined>
755
+ </Instrument-Model>
756
+ <Contact-Ref ref="contrib1" />
757
+ <Supplementary-Data type="TXT">
758
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649041/suppl/GSM4649041_Patient5_CpG.txt.gz
759
+ </Supplementary-Data>
760
+ <Relation type="BioSample" target="https://www.ncbi.nlm.nih.gov/biosample/SAMN15420258" />
761
+ <Relation type="SRA" target="https://www.ncbi.nlm.nih.gov/sra?term=SRX8651474" />
762
+ </Sample>
763
+
764
+ <Sample iid="GSM4649042">
765
+ <Status database="GEO">
766
+ <Submission-Date>2020-07-01</Submission-Date>
767
+ <Release-Date>2020-07-02</Release-Date>
768
+ <Last-Update-Date>2020-07-02</Last-Update-Date>
769
+ </Status>
770
+ <Title>Patient6</Title>
771
+ <Accession database="GEO">GSM4649042</Accession>
772
+ <Type>SRA</Type>
773
+ <Channel-Count>1</Channel-Count>
774
+ <Channel position="1">
775
+ <Source>Peripheral Blood Mononuclear Cells</Source>
776
+ <Organism taxid="9606">Homo sapiens</Organism>
777
+ <Characteristics tag="disease state">
778
+ Patient
779
+ </Characteristics>
780
+ <Molecule>genomic DNA</Molecule>
781
+ <Extract-Protocol>
782
+ DNA was extracted from 200ul of PBMCs
783
+ MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
784
+ </Extract-Protocol>
785
+ </Channel>
786
+ <Data-Processing>
787
+ reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
788
+ reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
789
+ bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
790
+ the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data
791
+ Genome_build: hg19
792
+ Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline.
793
+ Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). .
794
+ </Data-Processing>
795
+ <Platform-Ref ref="GPL16791" />
796
+ <Library-Strategy>Bisulfite-Seq</Library-Strategy>
797
+ <Library-Source>genomic</Library-Source>
798
+ <Library-Selection>Reduced Representation</Library-Selection>
799
+ <Instrument-Model>
800
+ <Predefined>Illumina HiSeq 2500</Predefined>
801
+ </Instrument-Model>
802
+ <Contact-Ref ref="contrib1" />
803
+ <Supplementary-Data type="TXT">
804
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649042/suppl/GSM4649042_Patient6_CpG.txt.gz
805
+ </Supplementary-Data>
806
+ <Relation type="BioSample" target="https://www.ncbi.nlm.nih.gov/biosample/SAMN15420257" />
807
+ <Relation type="SRA" target="https://www.ncbi.nlm.nih.gov/sra?term=SRX8651475" />
808
+ </Sample>
809
+
810
+ <Sample iid="GSM4649043">
811
+ <Status database="GEO">
812
+ <Submission-Date>2020-07-01</Submission-Date>
813
+ <Release-Date>2020-07-02</Release-Date>
814
+ <Last-Update-Date>2020-07-02</Last-Update-Date>
815
+ </Status>
816
+ <Title>Patient7</Title>
817
+ <Accession database="GEO">GSM4649043</Accession>
818
+ <Type>SRA</Type>
819
+ <Channel-Count>1</Channel-Count>
820
+ <Channel position="1">
821
+ <Source>Peripheral Blood Mononuclear Cells</Source>
822
+ <Organism taxid="9606">Homo sapiens</Organism>
823
+ <Characteristics tag="disease state">
824
+ Patient
825
+ </Characteristics>
826
+ <Molecule>genomic DNA</Molecule>
827
+ <Extract-Protocol>
828
+ DNA was extracted from 200ul of PBMCs
829
+ MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
830
+ </Extract-Protocol>
831
+ </Channel>
832
+ <Data-Processing>
833
+ reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
834
+ reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
835
+ bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
836
+ the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data
837
+ Genome_build: hg19
838
+ Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline.
839
+ Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). .
840
+ </Data-Processing>
841
+ <Platform-Ref ref="GPL16791" />
842
+ <Library-Strategy>Bisulfite-Seq</Library-Strategy>
843
+ <Library-Source>genomic</Library-Source>
844
+ <Library-Selection>Reduced Representation</Library-Selection>
845
+ <Instrument-Model>
846
+ <Predefined>Illumina HiSeq 2500</Predefined>
847
+ </Instrument-Model>
848
+ <Contact-Ref ref="contrib1" />
849
+ <Supplementary-Data type="TXT">
850
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649043/suppl/GSM4649043_Patient7_CpG.txt.gz
851
+ </Supplementary-Data>
852
+ <Relation type="BioSample" target="https://www.ncbi.nlm.nih.gov/biosample/SAMN15420256" />
853
+ <Relation type="SRA" target="https://www.ncbi.nlm.nih.gov/sra?term=SRX8651476" />
854
+ </Sample>
855
+
856
+ <Sample iid="GSM4649044">
857
+ <Status database="GEO">
858
+ <Submission-Date>2020-07-01</Submission-Date>
859
+ <Release-Date>2020-07-02</Release-Date>
860
+ <Last-Update-Date>2020-07-02</Last-Update-Date>
861
+ </Status>
862
+ <Title>Patient8</Title>
863
+ <Accession database="GEO">GSM4649044</Accession>
864
+ <Type>SRA</Type>
865
+ <Channel-Count>1</Channel-Count>
866
+ <Channel position="1">
867
+ <Source>Peripheral Blood Mononuclear Cells</Source>
868
+ <Organism taxid="9606">Homo sapiens</Organism>
869
+ <Characteristics tag="disease state">
870
+ Patient
871
+ </Characteristics>
872
+ <Molecule>genomic DNA</Molecule>
873
+ <Extract-Protocol>
874
+ DNA was extracted from 200ul of PBMCs
875
+ MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
876
+ </Extract-Protocol>
877
+ </Channel>
878
+ <Data-Processing>
879
+ reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
880
+ reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
881
+ bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
882
+ the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data
883
+ Genome_build: hg19
884
+ Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline.
885
+ Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). .
886
+ </Data-Processing>
887
+ <Platform-Ref ref="GPL16791" />
888
+ <Library-Strategy>Bisulfite-Seq</Library-Strategy>
889
+ <Library-Source>genomic</Library-Source>
890
+ <Library-Selection>Reduced Representation</Library-Selection>
891
+ <Instrument-Model>
892
+ <Predefined>Illumina HiSeq 2500</Predefined>
893
+ </Instrument-Model>
894
+ <Contact-Ref ref="contrib1" />
895
+ <Supplementary-Data type="TXT">
896
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649044/suppl/GSM4649044_Patient8_CpG.txt.gz
897
+ </Supplementary-Data>
898
+ <Relation type="BioSample" target="https://www.ncbi.nlm.nih.gov/biosample/SAMN15420255" />
899
+ <Relation type="SRA" target="https://www.ncbi.nlm.nih.gov/sra?term=SRX8651477" />
900
+ </Sample>
901
+
902
+ <Sample iid="GSM4649045">
903
+ <Status database="GEO">
904
+ <Submission-Date>2020-07-01</Submission-Date>
905
+ <Release-Date>2020-07-02</Release-Date>
906
+ <Last-Update-Date>2020-07-02</Last-Update-Date>
907
+ </Status>
908
+ <Title>Patient9</Title>
909
+ <Accession database="GEO">GSM4649045</Accession>
910
+ <Type>SRA</Type>
911
+ <Channel-Count>1</Channel-Count>
912
+ <Channel position="1">
913
+ <Source>Peripheral Blood Mononuclear Cells</Source>
914
+ <Organism taxid="9606">Homo sapiens</Organism>
915
+ <Characteristics tag="disease state">
916
+ Patient
917
+ </Characteristics>
918
+ <Molecule>genomic DNA</Molecule>
919
+ <Extract-Protocol>
920
+ DNA was extracted from 200ul of PBMCs
921
+ MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
922
+ </Extract-Protocol>
923
+ </Channel>
924
+ <Data-Processing>
925
+ reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
926
+ reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
927
+ bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
928
+ the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data
929
+ Genome_build: hg19
930
+ Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline.
931
+ Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). .
932
+ </Data-Processing>
933
+ <Platform-Ref ref="GPL16791" />
934
+ <Library-Strategy>Bisulfite-Seq</Library-Strategy>
935
+ <Library-Source>genomic</Library-Source>
936
+ <Library-Selection>Reduced Representation</Library-Selection>
937
+ <Instrument-Model>
938
+ <Predefined>Illumina HiSeq 2500</Predefined>
939
+ </Instrument-Model>
940
+ <Contact-Ref ref="contrib1" />
941
+ <Supplementary-Data type="TXT">
942
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649045/suppl/GSM4649045_Patient9_CpG.txt.gz
943
+ </Supplementary-Data>
944
+ <Relation type="BioSample" target="https://www.ncbi.nlm.nih.gov/biosample/SAMN15420254" />
945
+ <Relation type="SRA" target="https://www.ncbi.nlm.nih.gov/sra?term=SRX8651478" />
946
+ </Sample>
947
+
948
+ <Sample iid="GSM4649046">
949
+ <Status database="GEO">
950
+ <Submission-Date>2020-07-01</Submission-Date>
951
+ <Release-Date>2020-07-02</Release-Date>
952
+ <Last-Update-Date>2020-07-02</Last-Update-Date>
953
+ </Status>
954
+ <Title>Patient10</Title>
955
+ <Accession database="GEO">GSM4649046</Accession>
956
+ <Type>SRA</Type>
957
+ <Channel-Count>1</Channel-Count>
958
+ <Channel position="1">
959
+ <Source>Peripheral Blood Mononuclear Cells</Source>
960
+ <Organism taxid="9606">Homo sapiens</Organism>
961
+ <Characteristics tag="disease state">
962
+ Patient
963
+ </Characteristics>
964
+ <Molecule>genomic DNA</Molecule>
965
+ <Extract-Protocol>
966
+ DNA was extracted from 200ul of PBMCs
967
+ MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
968
+ </Extract-Protocol>
969
+ </Channel>
970
+ <Data-Processing>
971
+ reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
972
+ reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
973
+ bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
974
+ the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data
975
+ Genome_build: hg19
976
+ Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline.
977
+ Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). .
978
+ </Data-Processing>
979
+ <Platform-Ref ref="GPL16791" />
980
+ <Library-Strategy>Bisulfite-Seq</Library-Strategy>
981
+ <Library-Source>genomic</Library-Source>
982
+ <Library-Selection>Reduced Representation</Library-Selection>
983
+ <Instrument-Model>
984
+ <Predefined>Illumina HiSeq 2500</Predefined>
985
+ </Instrument-Model>
986
+ <Contact-Ref ref="contrib1" />
987
+ <Supplementary-Data type="TXT">
988
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649046/suppl/GSM4649046_Patient10_CpG.txt.gz
989
+ </Supplementary-Data>
990
+ <Relation type="BioSample" target="https://www.ncbi.nlm.nih.gov/biosample/SAMN15420253" />
991
+ <Relation type="SRA" target="https://www.ncbi.nlm.nih.gov/sra?term=SRX8651479" />
992
+ </Sample>
993
+
994
+ <Series iid="GSE153667">
995
+ <Status database="GEO">
996
+ <Submission-Date>2020-07-01</Submission-Date>
997
+ <Release-Date>2020-07-02</Release-Date>
998
+ <Last-Update-Date>2020-11-09</Last-Update-Date>
999
+ </Status>
1000
+ <Title>Changes in the Epigenetic Landscape of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Reflect Systemic Dysfunctions</Title>
1001
+ <Accession database="GEO">GSE153667</Accession>
1002
+ <Pubmed-ID>33148325</Pubmed-ID>
1003
+ <Summary>
1004
+ Purpose: ME/CFS is a lifelong debilitating disease that affects approximately 1% of the global population. Previous studies have identified dysfunctional activity in metabolic, immune and neurological pathways. The goal of this study is to identify ME/CFS specific variations in DNA methylation to determine whether the patient specific epigenetic patterns provide insight into the disease pathophysiology.
1005
+ Methods: DNA was extracted from the PBMCs of 10 ME/CFS patients and age/gender matched controls. After performing RRBS the sequence was aligned to hg19 genome using Bismark. The data was analyzed using first an ANOVA F test through DMAP in order to determine variation between the patient and control groups across 40-220bp fragments of the genome. Additional analysis was performed following a MethylKit pipeline, which analyzed the variation on a single CpG basis using a Fishers test.
1006
+ Results: From a total of 146,575 DMAP fragments we identified 76 differentially methylated fragments (P &lt;0.05, Diff meth +/- 15%). A total of 31 were associated with gene regions (intronic/exonic). MethylKit analysis also identified a total of 394 differentially methylated cytosines (FDR corrected P &lt;0.05, Diff meth +/- 15%) from a total of 196,172 individual analyzed cytosines, 91 of the statistically significant cytosines fell within gene regions. Comparison of both methylomes and regions where both the DMAP fragments and multiple MethylKit cytosines fell highlighted areas of the genome containing regulatory elements associated with metabolic and immune activity. Gene body pathway enrichment additionally identified immune metabolic and neurological related functions.
1007
+ Conclusions: Our study represents the first investigation of ME/CFS patients using reduced representation bisulfite sequencing. We identified a number of major differences between patients that distinguished them from healthy controls. Our results identified a number of differentially methylated regulatory elements and gene bodies that highlight the disturbed pathophysiology in ME/CFS. In particular the large number of enriched neurotransmitter and neuropeptide reactome pathways highlighted a disturbed neurological pathophysiology in patients.
1008
+ </Summary>
1009
+ <Overall-Design>
1010
+ RRBS Analysis of 10 ME/CFS patients vs. Controls
1011
+ </Overall-Design>
1012
+ <Type>Methylation profiling by high throughput sequencing</Type>
1013
+ <Contributor-Ref ref="contrib1" position="1" />
1014
+ <Contributor-Ref ref="contrib3" position="2" />
1015
+ <Contributor-Ref ref="contrib4" position="3" />
1016
+ <Contributor-Ref ref="contrib5" position="4" />
1017
+ <Contributor-Ref ref="contrib6" position="5" />
1018
+ <Contributor-Ref ref="contrib7" position="6" />
1019
+ <Contact-Ref ref="contrib1" />
1020
+ <Sample-Ref ref="GSM4649027" />
1021
+ <Sample-Ref ref="GSM4649028" />
1022
+ <Sample-Ref ref="GSM4649029" />
1023
+ <Sample-Ref ref="GSM4649030" />
1024
+ <Sample-Ref ref="GSM4649031" />
1025
+ <Sample-Ref ref="GSM4649032" />
1026
+ <Sample-Ref ref="GSM4649033" />
1027
+ <Sample-Ref ref="GSM4649034" />
1028
+ <Sample-Ref ref="GSM4649035" />
1029
+ <Sample-Ref ref="GSM4649036" />
1030
+ <Sample-Ref ref="GSM4649037" />
1031
+ <Sample-Ref ref="GSM4649038" />
1032
+ <Sample-Ref ref="GSM4649039" />
1033
+ <Sample-Ref ref="GSM4649040" />
1034
+ <Sample-Ref ref="GSM4649041" />
1035
+ <Sample-Ref ref="GSM4649042" />
1036
+ <Sample-Ref ref="GSM4649043" />
1037
+ <Sample-Ref ref="GSM4649044" />
1038
+ <Sample-Ref ref="GSM4649045" />
1039
+ <Sample-Ref ref="GSM4649046" />
1040
+ <Supplementary-Data type="CSV">
1041
+ ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE153nnn/GSE153667/suppl/GSE153667_DMAP_matrix.csv.gz
1042
+ </Supplementary-Data>
1043
+ <Supplementary-Data type="XLSX">
1044
+ ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE153nnn/GSE153667/suppl/GSE153667_GeneMatrix.xlsx
1045
+ </Supplementary-Data>
1046
+ <Supplementary-Data type="CSV">
1047
+ ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE153nnn/GSE153667/suppl/GSE153667_Meth_Matrix.csv.gz
1048
+ </Supplementary-Data>
1049
+ <Supplementary-Data type="TAR">
1050
+ ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE153nnn/GSE153667/suppl/GSE153667_RAW.tar
1051
+ </Supplementary-Data>
1052
+ <Relation type="BioProject" target="https://www.ncbi.nlm.nih.gov/bioproject/PRJNA643579" />
1053
+ <Relation type="SRA" target="https://www.ncbi.nlm.nih.gov/sra?term=SRP269624" />
1054
+ </Series>
1055
+
1056
+ </MINiML>
ME/GSE153667/meta/GSE153667_series_matrix.txt ADDED
@@ -0,0 +1,76 @@
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
1
+ !Series_title "Changes in the Epigenetic Landscape of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Reflect Systemic Dysfunctions"
2
+ !Series_geo_accession "GSE153667"
3
+ !Series_status "Public on Jul 02 2020"
4
+ !Series_submission_date "Jul 01 2020"
5
+ !Series_last_update_date "Nov 09 2020"
6
+ !Series_pubmed_id "33148325"
7
+ !Series_summary "Purpose: ME/CFS is a lifelong debilitating disease that affects approximately 1% of the global population. Previous studies have identified dysfunctional activity in metabolic, immune and neurological pathways. The goal of this study is to identify ME/CFS specific variations in DNA methylation to determine whether the patient specific epigenetic patterns provide insight into the disease pathophysiology."
8
+ !Series_summary "Methods: DNA was extracted from the PBMCs of 10 ME/CFS patients and age/gender matched controls. After performing RRBS the sequence was aligned to hg19 genome using Bismark. The data was analyzed using first an ANOVA F test through DMAP in order to determine variation between the patient and control groups across 40-220bp fragments of the genome. Additional analysis was performed following a MethylKit pipeline, which analyzed the variation on a single CpG basis using a Fishers test."
9
+ !Series_summary "Results: From a total of 146,575 DMAP fragments we identified 76 differentially methylated fragments (P <0.05, Diff meth +/- 15%). A total of 31 were associated with gene regions (intronic/exonic). MethylKit analysis also identified a total of 394 differentially methylated cytosines (FDR corrected P <0.05, Diff meth +/- 15%) from a total of 196,172 individual analyzed cytosines, 91 of the statistically significant cytosines fell within gene regions. Comparison of both methylomes and regions where both the DMAP fragments and multiple MethylKit cytosines fell highlighted areas of the genome containing regulatory elements associated with metabolic and immune activity. Gene body pathway enrichment additionally identified immune metabolic and neurological related functions."
10
+ !Series_summary "Conclusions: Our study represents the first investigation of ME/CFS patients using reduced representation bisulfite sequencing. We identified a number of major differences between patients that distinguished them from healthy controls. Our results identified a number of differentially methylated regulatory elements and gene bodies that highlight the disturbed pathophysiology in ME/CFS. In particular the large number of enriched neurotransmitter and neuropeptide reactome pathways highlighted a disturbed neurological pathophysiology in patients."
11
+ !Series_overall_design "RRBS Analysis of 10 ME/CFS patients vs. Controls"
12
+ !Series_type "Methylation profiling by high throughput sequencing"
13
+ !Series_contributor "Amber,,Helliwell"
14
+ !Series_contributor "Warren,,Tate"
15
+ !Series_contributor "Aniruddha,,Chatterjee"
16
+ !Series_contributor "Peter,,Stockwell"
17
+ !Series_contributor "Eiren,,Sweetman"
18
+ !Series_contributor "Tina,,Edgar"
19
+ !Series_sample_id "GSM4649027 GSM4649028 GSM4649029 GSM4649030 GSM4649031 GSM4649032 GSM4649033 GSM4649034 GSM4649035 GSM4649036 GSM4649037 GSM4649038 GSM4649039 GSM4649040 GSM4649041 GSM4649042 GSM4649043 GSM4649044 GSM4649045 GSM4649046 "
20
+ !Series_contact_name "Amber,,Helliwell"
21
+ !Series_contact_department "Biochemistry Department"
22
+ !Series_contact_institute "University of Otago"
23
+ !Series_contact_address "710 Cumberland Road"
24
+ !Series_contact_city "Dunedin"
25
+ !Series_contact_zip/postal_code "9016"
26
+ !Series_contact_country "New Zealand"
27
+ !Series_supplementary_file "ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE153nnn/GSE153667/suppl/GSE153667_DMAP_matrix.csv.gz"
28
+ !Series_supplementary_file "ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE153nnn/GSE153667/suppl/GSE153667_GeneMatrix.xlsx"
29
+ !Series_supplementary_file "ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE153nnn/GSE153667/suppl/GSE153667_Meth_Matrix.csv.gz"
30
+ !Series_supplementary_file "ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE153nnn/GSE153667/suppl/GSE153667_RAW.tar"
31
+ !Series_platform_id "GPL16791"
32
+ !Series_platform_taxid "9606"
33
+ !Series_sample_taxid "9606"
34
+ !Series_relation "BioProject: https://www.ncbi.nlm.nih.gov/bioproject/PRJNA643579"
35
+ !Series_relation "SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRP269624"
36
+
37
+ !Sample_title "Control1" "Control2" "Control3" "Control4" "Control5" "Control6" "Control7" "Control8" "Control9" "Control10" "Patient1" "Patient2" "Patient3" "Patient4" "Patient5" "Patient6" "Patient7" "Patient8" "Patient9" "Patient10"
38
+ !Sample_geo_accession "GSM4649027" "GSM4649028" "GSM4649029" "GSM4649030" "GSM4649031" "GSM4649032" "GSM4649033" "GSM4649034" "GSM4649035" "GSM4649036" "GSM4649037" "GSM4649038" "GSM4649039" "GSM4649040" "GSM4649041" "GSM4649042" "GSM4649043" "GSM4649044" "GSM4649045" "GSM4649046"
39
+ !Sample_status "Public on Jul 02 2020" "Public on Jul 02 2020" "Public on Jul 02 2020" "Public on Jul 02 2020" "Public on Jul 02 2020" "Public on Jul 02 2020" "Public on Jul 02 2020" "Public on Jul 02 2020" "Public on Jul 02 2020" "Public on Jul 02 2020" "Public on Jul 02 2020" "Public on Jul 02 2020" "Public on Jul 02 2020" "Public on Jul 02 2020" "Public on Jul 02 2020" "Public on Jul 02 2020" "Public on Jul 02 2020" "Public on Jul 02 2020" "Public on Jul 02 2020" "Public on Jul 02 2020"
40
+ !Sample_submission_date "Jul 01 2020" "Jul 01 2020" "Jul 01 2020" "Jul 01 2020" "Jul 01 2020" "Jul 01 2020" "Jul 01 2020" "Jul 01 2020" "Jul 01 2020" "Jul 01 2020" "Jul 01 2020" "Jul 01 2020" "Jul 01 2020" "Jul 01 2020" "Jul 01 2020" "Jul 01 2020" "Jul 01 2020" "Jul 01 2020" "Jul 01 2020" "Jul 01 2020"
41
+ !Sample_last_update_date "Jul 02 2020" "Jul 02 2020" "Jul 02 2020" "Jul 02 2020" "Jul 02 2020" "Jul 02 2020" "Jul 02 2020" "Jul 02 2020" "Jul 02 2020" "Jul 02 2020" "Jul 02 2020" "Jul 02 2020" "Jul 02 2020" "Jul 02 2020" "Jul 02 2020" "Jul 02 2020" "Jul 02 2020" "Jul 02 2020" "Jul 02 2020" "Jul 02 2020"
42
+ !Sample_type "SRA" "SRA" "SRA" "SRA" "SRA" "SRA" "SRA" "SRA" "SRA" "SRA" "SRA" "SRA" "SRA" "SRA" "SRA" "SRA" "SRA" "SRA" "SRA" "SRA"
43
+ !Sample_channel_count "1" "1" "1" "1" "1" "1" "1" "1" "1" "1" "1" "1" "1" "1" "1" "1" "1" "1" "1" "1"
44
+ !Sample_source_name_ch1 "Peripheral Blood Mononuclear Cells" "Peripheral Blood Mononuclear Cells" "Peripheral Blood Mononuclear Cells" "Peripheral Blood Mononuclear Cells" "Peripheral Blood Mononuclear Cells" "Peripheral Blood Mononuclear Cells" "Peripheral Blood Mononuclear Cells" "Peripheral Blood Mononuclear Cells" "Peripheral Blood Mononuclear Cells" "Peripheral Blood Mononuclear Cells" "Peripheral Blood Mononuclear Cells" "Peripheral Blood Mononuclear Cells" "Peripheral Blood Mononuclear Cells" "Peripheral Blood Mononuclear Cells" "Peripheral Blood Mononuclear Cells" "Peripheral Blood Mononuclear Cells" "Peripheral Blood Mononuclear Cells" "Peripheral Blood Mononuclear Cells" "Peripheral Blood Mononuclear Cells" "Peripheral Blood Mononuclear Cells"
45
+ !Sample_organism_ch1 "Homo sapiens" "Homo sapiens" "Homo sapiens" "Homo sapiens" "Homo sapiens" "Homo sapiens" "Homo sapiens" "Homo sapiens" "Homo sapiens" "Homo sapiens" "Homo sapiens" "Homo sapiens" "Homo sapiens" "Homo sapiens" "Homo sapiens" "Homo sapiens" "Homo sapiens" "Homo sapiens" "Homo sapiens" "Homo sapiens"
46
+ !Sample_characteristics_ch1 "disease state: Control" "disease state: Control" "disease state: Control" "disease state: Control" "disease state: Control" "disease state: Control" "disease state: Control" "disease state: Control" "disease state: Control" "disease state: Control" "disease state: Patient" "disease state: Patient" "disease state: Patient" "disease state: Patient" "disease state: Patient" "disease state: Patient" "disease state: Patient" "disease state: Patient" "disease state: Patient" "disease state: Patient"
47
+ !Sample_molecule_ch1 "genomic DNA" "genomic DNA" "genomic DNA" "genomic DNA" "genomic DNA" "genomic DNA" "genomic DNA" "genomic DNA" "genomic DNA" "genomic DNA" "genomic DNA" "genomic DNA" "genomic DNA" "genomic DNA" "genomic DNA" "genomic DNA" "genomic DNA" "genomic DNA" "genomic DNA" "genomic DNA"
48
+ !Sample_extract_protocol_ch1 "DNA was extracted from 200ul of PBMCs" "DNA was extracted from 200ul of PBMCs" "DNA was extracted from 200ul of PBMCs" "DNA was extracted from 200ul of PBMCs" "DNA was extracted from 200ul of PBMCs" "DNA was extracted from 200ul of PBMCs" "DNA was extracted from 200ul of PBMCs" "DNA was extracted from 200ul of PBMCs" "DNA was extracted from 200ul of PBMCs" "DNA was extracted from 200ul of PBMCs" "DNA was extracted from 200ul of PBMCs" "DNA was extracted from 200ul of PBMCs" "DNA was extracted from 200ul of PBMCs" "DNA was extracted from 200ul of PBMCs" "DNA was extracted from 200ul of PBMCs" "DNA was extracted from 200ul of PBMCs" "DNA was extracted from 200ul of PBMCs" "DNA was extracted from 200ul of PBMCs" "DNA was extracted from 200ul of PBMCs" "DNA was extracted from 200ul of PBMCs"
49
+ !Sample_extract_protocol_ch1 "MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)" "MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)" "MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)" "MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)" "MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)" "MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)" "MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)" "MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)" "MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)" "MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)" "MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)" "MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)" "MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)" "MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)" "MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)" "MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)" "MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)" "MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)" "MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)" "MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)"
50
+ !Sample_taxid_ch1 "9606" "9606" "9606" "9606" "9606" "9606" "9606" "9606" "9606" "9606" "9606" "9606" "9606" "9606" "9606" "9606" "9606" "9606" "9606" "9606"
51
+ !Sample_data_processing "reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp" "reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp" "reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp" "reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp" "reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp" "reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp" "reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp" "reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp" "reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp" "reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp" "reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp" "reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp" "reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp" "reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp" "reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp" "reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp" "reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp" "reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp" "reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp" "reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp"
52
+ !Sample_data_processing "reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible" "reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible" "reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible" "reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible" "reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible" "reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible" "reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible" "reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible" "reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible" "reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible" "reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible" "reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible" "reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible" "reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible" "reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible" "reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible" "reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible" "reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible" "reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible" "reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible"
53
+ !Sample_data_processing "bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data." "bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data." "bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data." "bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data." "bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data." "bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data." "bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data." "bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data." "bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data." "bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data." "bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data." "bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data." "bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data." "bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data." "bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data." "bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data." "bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data." "bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data." "bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data." "bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: ANOVA F test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data."
54
+ !Sample_data_processing "the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data" "the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data" "the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data" "the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data" "the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data" "the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data" "the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data" "the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data" "the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data" "the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data" "the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data" "the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data" "the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data" "the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data" "the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data" "the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data" "the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data" "the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data" "the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data" "the bam files were additionally analysed following a MethylKit based pipeline where first the data was filtered for low read coverage (less than 10 times coverage) and normalised basde on mean coverage distribution before comparing pooled patient and control groups using a Fisher's test. Methmatrix.csv file contains this data"
55
+ !Sample_data_processing "Genome_build: hg19" "Genome_build: hg19" "Genome_build: hg19" "Genome_build: hg19" "Genome_build: hg19" "Genome_build: hg19" "Genome_build: hg19" "Genome_build: hg19" "Genome_build: hg19" "Genome_build: hg19" "Genome_build: hg19" "Genome_build: hg19" "Genome_build: hg19" "Genome_build: hg19" "Genome_build: hg19" "Genome_build: hg19" "Genome_build: hg19" "Genome_build: hg19" "Genome_build: hg19" "Genome_build: hg19"
56
+ !Sample_data_processing "Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline." "Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline." "Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline." "Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline." "Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline." "Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline." "Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline." "Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline." "Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline." "Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline." "Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline." "Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline." "Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline." "Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline." "Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline." "Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline." "Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline." "Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline." "Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline." "Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. Matrix (csv file) containing methylation percentages for each sample used in the control vs patient analysis for the MethylKit single CpG pipeline."
57
+ !Sample_data_processing "Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). ." "Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). ." "Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). ." "Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). ." "Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). ." "Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). ." "Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). ." "Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). ." "Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). ." "Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). ." "Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). ." "Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). ." "Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). ." "Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). ." "Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). ." "Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). ." "Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). ." "Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). ." "Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). ." "Supplementary_files_format_and_content: A matrix containing the DMAP output data (individual sample percentages, significance values, associated genomic features, fragment length, CpG per fragment). ."
58
+ !Sample_platform_id "GPL16791" "GPL16791" "GPL16791" "GPL16791" "GPL16791" "GPL16791" "GPL16791" "GPL16791" "GPL16791" "GPL16791" "GPL16791" "GPL16791" "GPL16791" "GPL16791" "GPL16791" "GPL16791" "GPL16791" "GPL16791" "GPL16791" "GPL16791"
59
+ !Sample_contact_name "Amber,,Helliwell" "Amber,,Helliwell" "Amber,,Helliwell" "Amber,,Helliwell" "Amber,,Helliwell" "Amber,,Helliwell" "Amber,,Helliwell" "Amber,,Helliwell" "Amber,,Helliwell" "Amber,,Helliwell" "Amber,,Helliwell" "Amber,,Helliwell" "Amber,,Helliwell" "Amber,,Helliwell" "Amber,,Helliwell" "Amber,,Helliwell" "Amber,,Helliwell" "Amber,,Helliwell" "Amber,,Helliwell" "Amber,,Helliwell"
60
+ !Sample_contact_department "Biochemistry Department" "Biochemistry Department" "Biochemistry Department" "Biochemistry Department" "Biochemistry Department" "Biochemistry Department" "Biochemistry Department" "Biochemistry Department" "Biochemistry Department" "Biochemistry Department" "Biochemistry Department" "Biochemistry Department" "Biochemistry Department" "Biochemistry Department" "Biochemistry Department" "Biochemistry Department" "Biochemistry Department" "Biochemistry Department" "Biochemistry Department" "Biochemistry Department"
61
+ !Sample_contact_institute "University of Otago" "University of Otago" "University of Otago" "University of Otago" "University of Otago" "University of Otago" "University of Otago" "University of Otago" "University of Otago" "University of Otago" "University of Otago" "University of Otago" "University of Otago" "University of Otago" "University of Otago" "University of Otago" "University of Otago" "University of Otago" "University of Otago" "University of Otago"
62
+ !Sample_contact_address "710 Cumberland Road" "710 Cumberland Road" "710 Cumberland Road" "710 Cumberland Road" "710 Cumberland Road" "710 Cumberland Road" "710 Cumberland Road" "710 Cumberland Road" "710 Cumberland Road" "710 Cumberland Road" "710 Cumberland Road" "710 Cumberland Road" "710 Cumberland Road" "710 Cumberland Road" "710 Cumberland Road" "710 Cumberland Road" "710 Cumberland Road" "710 Cumberland Road" "710 Cumberland Road" "710 Cumberland Road"
63
+ !Sample_contact_city "Dunedin" "Dunedin" "Dunedin" "Dunedin" "Dunedin" "Dunedin" "Dunedin" "Dunedin" "Dunedin" "Dunedin" "Dunedin" "Dunedin" "Dunedin" "Dunedin" "Dunedin" "Dunedin" "Dunedin" "Dunedin" "Dunedin" "Dunedin"
64
+ !Sample_contact_zip/postal_code "9016" "9016" "9016" "9016" "9016" "9016" "9016" "9016" "9016" "9016" "9016" "9016" "9016" "9016" "9016" "9016" "9016" "9016" "9016" "9016"
65
+ !Sample_contact_country "New Zealand" "New Zealand" "New Zealand" "New Zealand" "New Zealand" "New Zealand" "New Zealand" "New Zealand" "New Zealand" "New Zealand" "New Zealand" "New Zealand" "New Zealand" "New Zealand" "New Zealand" "New Zealand" "New Zealand" "New Zealand" "New Zealand" "New Zealand"
66
+ !Sample_data_row_count "0" "0" "0" "0" "0" "0" "0" "0" "0" "0" "0" "0" "0" "0" "0" "0" "0" "0" "0" "0"
67
+ !Sample_instrument_model "Illumina HiSeq 2500" "Illumina HiSeq 2500" "Illumina HiSeq 2500" "Illumina HiSeq 2500" "Illumina HiSeq 2500" "Illumina HiSeq 2500" "Illumina HiSeq 2500" "Illumina HiSeq 2500" "Illumina HiSeq 2500" "Illumina HiSeq 2500" "Illumina HiSeq 2500" "Illumina HiSeq 2500" "Illumina HiSeq 2500" "Illumina HiSeq 2500" "Illumina HiSeq 2500" "Illumina HiSeq 2500" "Illumina HiSeq 2500" "Illumina HiSeq 2500" "Illumina HiSeq 2500" "Illumina HiSeq 2500"
68
+ !Sample_library_selection "Reduced Representation" "Reduced Representation" "Reduced Representation" "Reduced Representation" "Reduced Representation" "Reduced Representation" "Reduced Representation" "Reduced Representation" "Reduced Representation" "Reduced Representation" "Reduced Representation" "Reduced Representation" "Reduced Representation" "Reduced Representation" "Reduced Representation" "Reduced Representation" "Reduced Representation" "Reduced Representation" "Reduced Representation" "Reduced Representation"
69
+ !Sample_library_source "genomic" "genomic" "genomic" "genomic" "genomic" "genomic" "genomic" "genomic" "genomic" "genomic" "genomic" "genomic" "genomic" "genomic" "genomic" "genomic" "genomic" "genomic" "genomic" "genomic"
70
+ !Sample_library_strategy "Bisulfite-Seq" "Bisulfite-Seq" "Bisulfite-Seq" "Bisulfite-Seq" "Bisulfite-Seq" "Bisulfite-Seq" "Bisulfite-Seq" "Bisulfite-Seq" "Bisulfite-Seq" "Bisulfite-Seq" "Bisulfite-Seq" "Bisulfite-Seq" "Bisulfite-Seq" "Bisulfite-Seq" "Bisulfite-Seq" "Bisulfite-Seq" "Bisulfite-Seq" "Bisulfite-Seq" "Bisulfite-Seq" "Bisulfite-Seq"
71
+ !Sample_relation "BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN15420272" "BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN15420271" "BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN15420270" "BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN15420269" "BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN15420268" "BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN15420267" "BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN15420266" "BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN15420265" "BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN15420264" "BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN15420263" "BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN15420262" "BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN15420261" "BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN15420260" "BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN15420259" "BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN15420258" "BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN15420257" "BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN15420256" "BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN15420255" "BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN15420254" "BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN15420253"
72
+ !Sample_relation "SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX8651460" "SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX8651461" "SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX8651462" "SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX8651463" "SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX8651464" "SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX8651465" "SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX8651466" "SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX8651467" "SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX8651468" "SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX8651469" "SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX8651470" "SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX8651471" "SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX8651472" "SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX8651473" "SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX8651474" "SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX8651475" "SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX8651476" "SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX8651477" "SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX8651478" "SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX8651479"
73
+ !Sample_supplementary_file_1 "ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649027/suppl/GSM4649027_Control1_CpG.txt.gz" "ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649028/suppl/GSM4649028_Control2_CpG.txt.gz" "ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649029/suppl/GSM4649029_Control3_CpG.txt.gz" "ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649030/suppl/GSM4649030_Control4_CpG.txt.gz" "ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649031/suppl/GSM4649031_Control5_CpG.txt.gz" "ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649032/suppl/GSM4649032_Control6_CpG.txt.gz" "ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649033/suppl/GSM4649033_Control7_CpG.txt.gz" "ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649034/suppl/GSM4649034_Control8_CpG.txt.gz" "ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649035/suppl/GSM4649035_Control9_CpG.txt.gz" "ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649036/suppl/GSM4649036_Control10_CpG.txt.gz" "ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649037/suppl/GSM4649037_Patient1_CpG.txt.gz" "ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649038/suppl/GSM4649038_Patient2_CpG.txt.gz" "ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649039/suppl/GSM4649039_Patient3_CpG.txt.gz" "ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649040/suppl/GSM4649040_Patient4_CpG.txt.gz" "ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649041/suppl/GSM4649041_Patient5_CpG.txt.gz" "ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649042/suppl/GSM4649042_Patient6_CpG.txt.gz" "ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649043/suppl/GSM4649043_Patient7_CpG.txt.gz" "ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649044/suppl/GSM4649044_Patient8_CpG.txt.gz" "ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649045/suppl/GSM4649045_Patient9_CpG.txt.gz" "ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM4649nnn/GSM4649046/suppl/GSM4649046_Patient10_CpG.txt.gz"
74
+ !series_matrix_table_begin
75
+ "ID_REF" "GSM4649027" "GSM4649028" "GSM4649029" "GSM4649030" "GSM4649031" "GSM4649032" "GSM4649033" "GSM4649034" "GSM4649035" "GSM4649036" "GSM4649037" "GSM4649038" "GSM4649039" "GSM4649040" "GSM4649041" "GSM4649042" "GSM4649043" "GSM4649044" "GSM4649045" "GSM4649046"
76
+ !series_matrix_table_end
ME/GSE156792/._GSE156792_detection_pval.txt ADDED
Binary file (4.1 kB). View file
 
ME/GSE156792/._GSE156792_meth_intensities.txt ADDED
Binary file (4.1 kB). View file
 
ME/GSE166592/GSE166592_RAW/GSM5076049_ME007E_CpG.txt ADDED
The diff for this file is too large to render. See raw diff
 
ME/GSE166592/meta/._GSE166592_family.soft ADDED
Binary file (4.1 kB). View file
 
ME/GSE166592/meta/._GSE166592_family.xml ADDED
Binary file (4.1 kB). View file
 
ME/GSE166592/meta/._GSE166592_series_matrix.txt ADDED
Binary file (4.1 kB). View file
 
ME/GSE166592/meta/GSE166592_family.soft ADDED
@@ -0,0 +1,681 @@
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
1
+ ^DATABASE = GeoMiame
2
+ !Database_name = Gene Expression Omnibus (GEO)
3
+ !Database_institute = NCBI NLM NIH
4
+ !Database_web_link = http://www.ncbi.nlm.nih.gov/geo
5
+ !Database_email = geo@ncbi.nlm.nih.gov
6
+ ^SERIES = GSE166592
7
+ !Series_title = Dynamic Epigenetic Changes during a Relapse and Recovery Cycle in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome
8
+ !Series_geo_accession = GSE166592
9
+ !Series_status = Public on Feb 11 2021
10
+ !Series_submission_date = Feb 10 2021
11
+ !Series_last_update_date = Mar 17 2021
12
+ !Series_summary = Purpose: ME/CFS is a debilitating and complex disease. The majority of patients exist in a chronic state of health where they are affected by relapse events. Precision medicine following patients can capture changes in the DNA methylation indicative of biological dysfunction
13
+ !Series_summary = Methods: DNA was extracted from the PBMCs of 2 ME/CFS patients and a age/gender matched control at five different time points. After performing RRBS the sequence was aligned to hg19 genome using Bismark. The data was analyzed using a Chi squared test through DMAP in order to determine variation between the patient and control groups across 40-220bp fragments of the genome.
14
+ !Series_summary = Results: A total of 17 and 14 statistically significant variably methylated fragements were indentified in each patient that strongly associated with a relapse event. These fragements were found on regions of regulatory importance of the genome that associated with immune (primarily inflammatory) and metabolic function.
15
+ !Series_summary = Conclusions: Our study represents the first investigation of ME/CFS patients using reduced representation bisulfite sequencing along a longitudinal timeframe. We captured a number of major variably methylated fragments in each patient that associated with their relapse events. Our results identified a number of differentially methylated regulatory elements and gene bodies that highlight the disturbed pathophysiology in ME/CFS. DNA methylation that differentiates disease variability in ongoing ME/CFS may have practical applications for strategies to deacrease the frequency and severity of relapse events.
16
+ !Series_overall_design = RRBS Analysis of 2 ME/CFS patients and matched control over eleven months
17
+ !Series_type = Methylation profiling by high throughput sequencing
18
+ !Series_contributor = Amber,,Helliwell
19
+ !Series_contributor = Warren,,Tate
20
+ !Series_contributor = Aniruddha,,Chatterjee
21
+ !Series_contributor = Peter,,Stockwell
22
+ !Series_contributor = Tina,,Edgar
23
+ !Series_sample_id = GSM5076040
24
+ !Series_sample_id = GSM5076041
25
+ !Series_sample_id = GSM5076042
26
+ !Series_sample_id = GSM5076043
27
+ !Series_sample_id = GSM5076044
28
+ !Series_sample_id = GSM5076045
29
+ !Series_sample_id = GSM5076046
30
+ !Series_sample_id = GSM5076047
31
+ !Series_sample_id = GSM5076048
32
+ !Series_sample_id = GSM5076049
33
+ !Series_sample_id = GSM5076050
34
+ !Series_sample_id = GSM5076051
35
+ !Series_sample_id = GSM5076052
36
+ !Series_sample_id = GSM5076053
37
+ !Series_sample_id = GSM5076054
38
+ !Series_contact_name = Amber,,Helliwell
39
+ !Series_contact_department = Biochemistry Department
40
+ !Series_contact_institute = University of Otago
41
+ !Series_contact_address = 710 Cumberland Road
42
+ !Series_contact_city = Dunedin
43
+ !Series_contact_zip/postal_code = 9016
44
+ !Series_contact_country = New Zealand
45
+ !Series_supplementary_file = ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE166nnn/GSE166592/suppl/GSE166592_C012_Full.xlsx
46
+ !Series_supplementary_file = ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE166nnn/GSE166592/suppl/GSE166592_ME007_Full.xlsx
47
+ !Series_supplementary_file = ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE166nnn/GSE166592/suppl/GSE166592_ME016_Full.xlsx
48
+ !Series_supplementary_file = ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE166nnn/GSE166592/suppl/GSE166592_RAW.tar
49
+ !Series_platform_id = GPL16791
50
+ !Series_platform_taxid = 9606
51
+ !Series_sample_taxid = 9606
52
+ !Series_relation = BioProject: https://www.ncbi.nlm.nih.gov/bioproject/PRJNA701322
53
+ !Series_relation = SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRP305748
54
+ ^PLATFORM = GPL16791
55
+ !Platform_title = Illumina HiSeq 2500 (Homo sapiens)
56
+ !Platform_geo_accession = GPL16791
57
+ !Platform_status = Public on Mar 14 2013
58
+ !Platform_submission_date = Mar 14 2013
59
+ !Platform_last_update_date = Mar 27 2019
60
+ !Platform_technology = high-throughput sequencing
61
+ !Platform_distribution = virtual
62
+ !Platform_organism = Homo sapiens
63
+ !Platform_taxid = 9606
64
+ !Platform_contact_name = ,,GEO
65
+ !Platform_contact_country = USA
66
+ !Platform_data_row_count = 0
67
+ ^SAMPLE = GSM5076040
68
+ !Sample_title = C012A
69
+ !Sample_geo_accession = GSM5076040
70
+ !Sample_status = Public on Feb 11 2021
71
+ !Sample_submission_date = Feb 10 2021
72
+ !Sample_last_update_date = Feb 12 2021
73
+ !Sample_type = SRA
74
+ !Sample_channel_count = 1
75
+ !Sample_source_name_ch1 = Peripheral Blood Mononuclear Cells
76
+ !Sample_organism_ch1 = Homo sapiens
77
+ !Sample_taxid_ch1 = 9606
78
+ !Sample_characteristics_ch1 = disease state: Control
79
+ !Sample_characteristics_ch1 = individual: C012
80
+ !Sample_characteristics_ch1 = time point: A
81
+ !Sample_characteristics_ch1 = cell type: Peripheral Blood Mononuclear Cells
82
+ !Sample_molecule_ch1 = genomic DNA
83
+ !Sample_extract_protocol_ch1 = DNA was extracted from 200ul of PBMCs
84
+ !Sample_extract_protocol_ch1 = MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
85
+ !Sample_description = C012A
86
+ !Sample_data_processing = reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
87
+ !Sample_data_processing = reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
88
+ !Sample_data_processing = bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: Chi squared test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
89
+ !Sample_data_processing = Genome_build: hg19
90
+ !Sample_data_processing = Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. C012_Full, ME007_Full and ME016_Full are excel files that contain, for the control, patient one, and patient two respectively, information about the per fragment methylation data including, genomic location, gene feature information, CpG relative location and fragment size.
91
+ !Sample_platform_id = GPL16791
92
+ !Sample_contact_name = Amber,,Helliwell
93
+ !Sample_contact_department = Biochemistry Department
94
+ !Sample_contact_institute = University of Otago
95
+ !Sample_contact_address = 710 Cumberland Road
96
+ !Sample_contact_city = Dunedin
97
+ !Sample_contact_zip/postal_code = 9016
98
+ !Sample_contact_country = New Zealand
99
+ !Sample_instrument_model = Illumina HiSeq 2500
100
+ !Sample_library_selection = Reduced Representation
101
+ !Sample_library_source = genomic
102
+ !Sample_library_strategy = Bisulfite-Seq
103
+ !Sample_relation = BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN17862810
104
+ !Sample_relation = SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX10073447
105
+ !Sample_supplementary_file_1 = ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM5076nnn/GSM5076040/suppl/GSM5076040_C012A_CpG.txt.gz
106
+ !Sample_series_id = GSE166592
107
+ !Sample_data_row_count = 0
108
+ ^SAMPLE = GSM5076041
109
+ !Sample_title = C012B
110
+ !Sample_geo_accession = GSM5076041
111
+ !Sample_status = Public on Feb 11 2021
112
+ !Sample_submission_date = Feb 10 2021
113
+ !Sample_last_update_date = Feb 12 2021
114
+ !Sample_type = SRA
115
+ !Sample_channel_count = 1
116
+ !Sample_source_name_ch1 = Peripheral Blood Mononuclear Cells
117
+ !Sample_organism_ch1 = Homo sapiens
118
+ !Sample_taxid_ch1 = 9606
119
+ !Sample_characteristics_ch1 = disease state: Control
120
+ !Sample_characteristics_ch1 = individual: C012
121
+ !Sample_characteristics_ch1 = time point: B
122
+ !Sample_characteristics_ch1 = cell type: Peripheral Blood Mononuclear Cells
123
+ !Sample_molecule_ch1 = genomic DNA
124
+ !Sample_extract_protocol_ch1 = DNA was extracted from 200ul of PBMCs
125
+ !Sample_extract_protocol_ch1 = MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
126
+ !Sample_description = C012B
127
+ !Sample_data_processing = reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
128
+ !Sample_data_processing = reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
129
+ !Sample_data_processing = bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: Chi squared test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
130
+ !Sample_data_processing = Genome_build: hg19
131
+ !Sample_data_processing = Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. C012_Full, ME007_Full and ME016_Full are excel files that contain, for the control, patient one, and patient two respectively, information about the per fragment methylation data including, genomic location, gene feature information, CpG relative location and fragment size.
132
+ !Sample_platform_id = GPL16791
133
+ !Sample_contact_name = Amber,,Helliwell
134
+ !Sample_contact_department = Biochemistry Department
135
+ !Sample_contact_institute = University of Otago
136
+ !Sample_contact_address = 710 Cumberland Road
137
+ !Sample_contact_city = Dunedin
138
+ !Sample_contact_zip/postal_code = 9016
139
+ !Sample_contact_country = New Zealand
140
+ !Sample_instrument_model = Illumina HiSeq 2500
141
+ !Sample_library_selection = Reduced Representation
142
+ !Sample_library_source = genomic
143
+ !Sample_library_strategy = Bisulfite-Seq
144
+ !Sample_relation = BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN17862809
145
+ !Sample_relation = SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX10073448
146
+ !Sample_supplementary_file_1 = ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM5076nnn/GSM5076041/suppl/GSM5076041_C012B_CpG.txt.gz
147
+ !Sample_series_id = GSE166592
148
+ !Sample_data_row_count = 0
149
+ ^SAMPLE = GSM5076042
150
+ !Sample_title = C012C
151
+ !Sample_geo_accession = GSM5076042
152
+ !Sample_status = Public on Feb 11 2021
153
+ !Sample_submission_date = Feb 10 2021
154
+ !Sample_last_update_date = Feb 12 2021
155
+ !Sample_type = SRA
156
+ !Sample_channel_count = 1
157
+ !Sample_source_name_ch1 = Peripheral Blood Mononuclear Cells
158
+ !Sample_organism_ch1 = Homo sapiens
159
+ !Sample_taxid_ch1 = 9606
160
+ !Sample_characteristics_ch1 = disease state: Control
161
+ !Sample_characteristics_ch1 = individual: C012
162
+ !Sample_characteristics_ch1 = time point: C
163
+ !Sample_characteristics_ch1 = cell type: Peripheral Blood Mononuclear Cells
164
+ !Sample_molecule_ch1 = genomic DNA
165
+ !Sample_extract_protocol_ch1 = DNA was extracted from 200ul of PBMCs
166
+ !Sample_extract_protocol_ch1 = MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
167
+ !Sample_description = C012C
168
+ !Sample_data_processing = reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
169
+ !Sample_data_processing = reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
170
+ !Sample_data_processing = bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: Chi squared test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
171
+ !Sample_data_processing = Genome_build: hg19
172
+ !Sample_data_processing = Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. C012_Full, ME007_Full and ME016_Full are excel files that contain, for the control, patient one, and patient two respectively, information about the per fragment methylation data including, genomic location, gene feature information, CpG relative location and fragment size.
173
+ !Sample_platform_id = GPL16791
174
+ !Sample_contact_name = Amber,,Helliwell
175
+ !Sample_contact_department = Biochemistry Department
176
+ !Sample_contact_institute = University of Otago
177
+ !Sample_contact_address = 710 Cumberland Road
178
+ !Sample_contact_city = Dunedin
179
+ !Sample_contact_zip/postal_code = 9016
180
+ !Sample_contact_country = New Zealand
181
+ !Sample_instrument_model = Illumina HiSeq 2500
182
+ !Sample_library_selection = Reduced Representation
183
+ !Sample_library_source = genomic
184
+ !Sample_library_strategy = Bisulfite-Seq
185
+ !Sample_relation = BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN17862808
186
+ !Sample_relation = SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX10073449
187
+ !Sample_supplementary_file_1 = ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM5076nnn/GSM5076042/suppl/GSM5076042_C012C_CpG.txt.gz
188
+ !Sample_series_id = GSE166592
189
+ !Sample_data_row_count = 0
190
+ ^SAMPLE = GSM5076043
191
+ !Sample_title = C012D
192
+ !Sample_geo_accession = GSM5076043
193
+ !Sample_status = Public on Feb 11 2021
194
+ !Sample_submission_date = Feb 10 2021
195
+ !Sample_last_update_date = Feb 12 2021
196
+ !Sample_type = SRA
197
+ !Sample_channel_count = 1
198
+ !Sample_source_name_ch1 = Peripheral Blood Mononuclear Cells
199
+ !Sample_organism_ch1 = Homo sapiens
200
+ !Sample_taxid_ch1 = 9606
201
+ !Sample_characteristics_ch1 = disease state: Control
202
+ !Sample_characteristics_ch1 = individual: C012
203
+ !Sample_characteristics_ch1 = time point: D
204
+ !Sample_characteristics_ch1 = cell type: Peripheral Blood Mononuclear Cells
205
+ !Sample_molecule_ch1 = genomic DNA
206
+ !Sample_extract_protocol_ch1 = DNA was extracted from 200ul of PBMCs
207
+ !Sample_extract_protocol_ch1 = MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
208
+ !Sample_description = C012D
209
+ !Sample_data_processing = reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
210
+ !Sample_data_processing = reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
211
+ !Sample_data_processing = bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: Chi squared test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
212
+ !Sample_data_processing = Genome_build: hg19
213
+ !Sample_data_processing = Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. C012_Full, ME007_Full and ME016_Full are excel files that contain, for the control, patient one, and patient two respectively, information about the per fragment methylation data including, genomic location, gene feature information, CpG relative location and fragment size.
214
+ !Sample_platform_id = GPL16791
215
+ !Sample_contact_name = Amber,,Helliwell
216
+ !Sample_contact_department = Biochemistry Department
217
+ !Sample_contact_institute = University of Otago
218
+ !Sample_contact_address = 710 Cumberland Road
219
+ !Sample_contact_city = Dunedin
220
+ !Sample_contact_zip/postal_code = 9016
221
+ !Sample_contact_country = New Zealand
222
+ !Sample_instrument_model = Illumina HiSeq 2500
223
+ !Sample_library_selection = Reduced Representation
224
+ !Sample_library_source = genomic
225
+ !Sample_library_strategy = Bisulfite-Seq
226
+ !Sample_relation = BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN17862807
227
+ !Sample_relation = SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX10073450
228
+ !Sample_supplementary_file_1 = ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM5076nnn/GSM5076043/suppl/GSM5076043_C012D_CpG.txt.gz
229
+ !Sample_series_id = GSE166592
230
+ !Sample_data_row_count = 0
231
+ ^SAMPLE = GSM5076044
232
+ !Sample_title = C012E
233
+ !Sample_geo_accession = GSM5076044
234
+ !Sample_status = Public on Feb 11 2021
235
+ !Sample_submission_date = Feb 10 2021
236
+ !Sample_last_update_date = Feb 12 2021
237
+ !Sample_type = SRA
238
+ !Sample_channel_count = 1
239
+ !Sample_source_name_ch1 = Peripheral Blood Mononuclear Cells
240
+ !Sample_organism_ch1 = Homo sapiens
241
+ !Sample_taxid_ch1 = 9606
242
+ !Sample_characteristics_ch1 = disease state: Control
243
+ !Sample_characteristics_ch1 = individual: C012
244
+ !Sample_characteristics_ch1 = time point: E
245
+ !Sample_characteristics_ch1 = cell type: Peripheral Blood Mononuclear Cells
246
+ !Sample_molecule_ch1 = genomic DNA
247
+ !Sample_extract_protocol_ch1 = DNA was extracted from 200ul of PBMCs
248
+ !Sample_extract_protocol_ch1 = MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
249
+ !Sample_description = C012E
250
+ !Sample_data_processing = reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
251
+ !Sample_data_processing = reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
252
+ !Sample_data_processing = bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: Chi squared test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
253
+ !Sample_data_processing = Genome_build: hg19
254
+ !Sample_data_processing = Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. C012_Full, ME007_Full and ME016_Full are excel files that contain, for the control, patient one, and patient two respectively, information about the per fragment methylation data including, genomic location, gene feature information, CpG relative location and fragment size.
255
+ !Sample_platform_id = GPL16791
256
+ !Sample_contact_name = Amber,,Helliwell
257
+ !Sample_contact_department = Biochemistry Department
258
+ !Sample_contact_institute = University of Otago
259
+ !Sample_contact_address = 710 Cumberland Road
260
+ !Sample_contact_city = Dunedin
261
+ !Sample_contact_zip/postal_code = 9016
262
+ !Sample_contact_country = New Zealand
263
+ !Sample_instrument_model = Illumina HiSeq 2500
264
+ !Sample_library_selection = Reduced Representation
265
+ !Sample_library_source = genomic
266
+ !Sample_library_strategy = Bisulfite-Seq
267
+ !Sample_relation = BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN17862806
268
+ !Sample_relation = SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX10073451
269
+ !Sample_supplementary_file_1 = ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM5076nnn/GSM5076044/suppl/GSM5076044_C012E_CpG.txt.gz
270
+ !Sample_series_id = GSE166592
271
+ !Sample_data_row_count = 0
272
+ ^SAMPLE = GSM5076045
273
+ !Sample_title = Patient_One_A
274
+ !Sample_geo_accession = GSM5076045
275
+ !Sample_status = Public on Feb 11 2021
276
+ !Sample_submission_date = Feb 10 2021
277
+ !Sample_last_update_date = Mar 17 2021
278
+ !Sample_type = SRA
279
+ !Sample_channel_count = 1
280
+ !Sample_source_name_ch1 = Peripheral Blood Mononuclear Cells
281
+ !Sample_organism_ch1 = Homo sapiens
282
+ !Sample_taxid_ch1 = 9606
283
+ !Sample_characteristics_ch1 = disease state: myalgic encephalomyelitis/chronic fatigue syndrome
284
+ !Sample_characteristics_ch1 = individual: Patient_One
285
+ !Sample_characteristics_ch1 = time point: A
286
+ !Sample_characteristics_ch1 = cell type: Peripheral Blood Mononuclear Cells
287
+ !Sample_molecule_ch1 = genomic DNA
288
+ !Sample_extract_protocol_ch1 = DNA was extracted from 200ul of PBMCs
289
+ !Sample_extract_protocol_ch1 = MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
290
+ !Sample_description = ME007A
291
+ !Sample_data_processing = reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
292
+ !Sample_data_processing = reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
293
+ !Sample_data_processing = bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: Chi squared test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
294
+ !Sample_data_processing = Genome_build: hg19
295
+ !Sample_data_processing = Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. C012_Full, ME007_Full and ME016_Full are excel files that contain, for the control, patient one, and patient two respectively, information about the per fragment methylation data including, genomic location, gene feature information, CpG relative location and fragment size.
296
+ !Sample_platform_id = GPL16791
297
+ !Sample_contact_name = Amber,,Helliwell
298
+ !Sample_contact_department = Biochemistry Department
299
+ !Sample_contact_institute = University of Otago
300
+ !Sample_contact_address = 710 Cumberland Road
301
+ !Sample_contact_city = Dunedin
302
+ !Sample_contact_zip/postal_code = 9016
303
+ !Sample_contact_country = New Zealand
304
+ !Sample_instrument_model = Illumina HiSeq 2500
305
+ !Sample_library_selection = Reduced Representation
306
+ !Sample_library_source = genomic
307
+ !Sample_library_strategy = Bisulfite-Seq
308
+ !Sample_relation = BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN17862805
309
+ !Sample_relation = SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX10073452
310
+ !Sample_supplementary_file_1 = ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM5076nnn/GSM5076045/suppl/GSM5076045_ME007A_CpG.txt.gz
311
+ !Sample_series_id = GSE166592
312
+ !Sample_data_row_count = 0
313
+ ^SAMPLE = GSM5076046
314
+ !Sample_title = Patient_One_B
315
+ !Sample_geo_accession = GSM5076046
316
+ !Sample_status = Public on Feb 11 2021
317
+ !Sample_submission_date = Feb 10 2021
318
+ !Sample_last_update_date = Feb 12 2021
319
+ !Sample_type = SRA
320
+ !Sample_channel_count = 1
321
+ !Sample_source_name_ch1 = Peripheral Blood Mononuclear Cells
322
+ !Sample_organism_ch1 = Homo sapiens
323
+ !Sample_taxid_ch1 = 9606
324
+ !Sample_characteristics_ch1 = disease state: myalgic encephalomyelitis/chronic fatigue syndrome
325
+ !Sample_characteristics_ch1 = individual: Patient_One
326
+ !Sample_characteristics_ch1 = time point: B
327
+ !Sample_characteristics_ch1 = cell type: Peripheral Blood Mononuclear Cells
328
+ !Sample_molecule_ch1 = genomic DNA
329
+ !Sample_extract_protocol_ch1 = DNA was extracted from 200ul of PBMCs
330
+ !Sample_extract_protocol_ch1 = MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
331
+ !Sample_description = ME007B
332
+ !Sample_data_processing = reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
333
+ !Sample_data_processing = reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
334
+ !Sample_data_processing = bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: Chi squared test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
335
+ !Sample_data_processing = Genome_build: hg19
336
+ !Sample_data_processing = Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. C012_Full, ME007_Full and ME016_Full are excel files that contain, for the control, patient one, and patient two respectively, information about the per fragment methylation data including, genomic location, gene feature information, CpG relative location and fragment size.
337
+ !Sample_platform_id = GPL16791
338
+ !Sample_contact_name = Amber,,Helliwell
339
+ !Sample_contact_department = Biochemistry Department
340
+ !Sample_contact_institute = University of Otago
341
+ !Sample_contact_address = 710 Cumberland Road
342
+ !Sample_contact_city = Dunedin
343
+ !Sample_contact_zip/postal_code = 9016
344
+ !Sample_contact_country = New Zealand
345
+ !Sample_instrument_model = Illumina HiSeq 2500
346
+ !Sample_library_selection = Reduced Representation
347
+ !Sample_library_source = genomic
348
+ !Sample_library_strategy = Bisulfite-Seq
349
+ !Sample_relation = BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN17862804
350
+ !Sample_relation = SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX10073453
351
+ !Sample_supplementary_file_1 = ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM5076nnn/GSM5076046/suppl/GSM5076046_ME007B_CpG.txt.gz
352
+ !Sample_series_id = GSE166592
353
+ !Sample_data_row_count = 0
354
+ ^SAMPLE = GSM5076047
355
+ !Sample_title = Patient_One_C
356
+ !Sample_geo_accession = GSM5076047
357
+ !Sample_status = Public on Feb 11 2021
358
+ !Sample_submission_date = Feb 10 2021
359
+ !Sample_last_update_date = Feb 12 2021
360
+ !Sample_type = SRA
361
+ !Sample_channel_count = 1
362
+ !Sample_source_name_ch1 = Peripheral Blood Mononuclear Cells
363
+ !Sample_organism_ch1 = Homo sapiens
364
+ !Sample_taxid_ch1 = 9606
365
+ !Sample_characteristics_ch1 = disease state: myalgic encephalomyelitis/chronic fatigue syndrome
366
+ !Sample_characteristics_ch1 = individual: Patient_One
367
+ !Sample_characteristics_ch1 = time point: C
368
+ !Sample_characteristics_ch1 = cell type: Peripheral Blood Mononuclear Cells
369
+ !Sample_molecule_ch1 = genomic DNA
370
+ !Sample_extract_protocol_ch1 = DNA was extracted from 200ul of PBMCs
371
+ !Sample_extract_protocol_ch1 = MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
372
+ !Sample_description = ME007C
373
+ !Sample_data_processing = reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
374
+ !Sample_data_processing = reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
375
+ !Sample_data_processing = bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: Chi squared test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
376
+ !Sample_data_processing = Genome_build: hg19
377
+ !Sample_data_processing = Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. C012_Full, ME007_Full and ME016_Full are excel files that contain, for the control, patient one, and patient two respectively, information about the per fragment methylation data including, genomic location, gene feature information, CpG relative location and fragment size.
378
+ !Sample_platform_id = GPL16791
379
+ !Sample_contact_name = Amber,,Helliwell
380
+ !Sample_contact_department = Biochemistry Department
381
+ !Sample_contact_institute = University of Otago
382
+ !Sample_contact_address = 710 Cumberland Road
383
+ !Sample_contact_city = Dunedin
384
+ !Sample_contact_zip/postal_code = 9016
385
+ !Sample_contact_country = New Zealand
386
+ !Sample_instrument_model = Illumina HiSeq 2500
387
+ !Sample_library_selection = Reduced Representation
388
+ !Sample_library_source = genomic
389
+ !Sample_library_strategy = Bisulfite-Seq
390
+ !Sample_relation = BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN17862803
391
+ !Sample_relation = SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX10073454
392
+ !Sample_supplementary_file_1 = ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM5076nnn/GSM5076047/suppl/GSM5076047_ME007C_CpG.txt.gz
393
+ !Sample_series_id = GSE166592
394
+ !Sample_data_row_count = 0
395
+ ^SAMPLE = GSM5076048
396
+ !Sample_title = Patient_One_D
397
+ !Sample_geo_accession = GSM5076048
398
+ !Sample_status = Public on Feb 11 2021
399
+ !Sample_submission_date = Feb 10 2021
400
+ !Sample_last_update_date = Feb 12 2021
401
+ !Sample_type = SRA
402
+ !Sample_channel_count = 1
403
+ !Sample_source_name_ch1 = Peripheral Blood Mononuclear Cells
404
+ !Sample_organism_ch1 = Homo sapiens
405
+ !Sample_taxid_ch1 = 9606
406
+ !Sample_characteristics_ch1 = disease state: myalgic encephalomyelitis/chronic fatigue syndrome
407
+ !Sample_characteristics_ch1 = individual: Patient_One
408
+ !Sample_characteristics_ch1 = time point: D
409
+ !Sample_characteristics_ch1 = cell type: Peripheral Blood Mononuclear Cells
410
+ !Sample_molecule_ch1 = genomic DNA
411
+ !Sample_extract_protocol_ch1 = DNA was extracted from 200ul of PBMCs
412
+ !Sample_extract_protocol_ch1 = MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
413
+ !Sample_description = ME007D
414
+ !Sample_data_processing = reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
415
+ !Sample_data_processing = reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
416
+ !Sample_data_processing = bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: Chi squared test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
417
+ !Sample_data_processing = Genome_build: hg19
418
+ !Sample_data_processing = Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. C012_Full, ME007_Full and ME016_Full are excel files that contain, for the control, patient one, and patient two respectively, information about the per fragment methylation data including, genomic location, gene feature information, CpG relative location and fragment size.
419
+ !Sample_platform_id = GPL16791
420
+ !Sample_contact_name = Amber,,Helliwell
421
+ !Sample_contact_department = Biochemistry Department
422
+ !Sample_contact_institute = University of Otago
423
+ !Sample_contact_address = 710 Cumberland Road
424
+ !Sample_contact_city = Dunedin
425
+ !Sample_contact_zip/postal_code = 9016
426
+ !Sample_contact_country = New Zealand
427
+ !Sample_instrument_model = Illumina HiSeq 2500
428
+ !Sample_library_selection = Reduced Representation
429
+ !Sample_library_source = genomic
430
+ !Sample_library_strategy = Bisulfite-Seq
431
+ !Sample_relation = BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN17862802
432
+ !Sample_relation = SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX10073455
433
+ !Sample_supplementary_file_1 = ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM5076nnn/GSM5076048/suppl/GSM5076048_ME007D_CpG.txt.gz
434
+ !Sample_series_id = GSE166592
435
+ !Sample_data_row_count = 0
436
+ ^SAMPLE = GSM5076049
437
+ !Sample_title = Patient_One_E
438
+ !Sample_geo_accession = GSM5076049
439
+ !Sample_status = Public on Feb 11 2021
440
+ !Sample_submission_date = Feb 10 2021
441
+ !Sample_last_update_date = Feb 12 2021
442
+ !Sample_type = SRA
443
+ !Sample_channel_count = 1
444
+ !Sample_source_name_ch1 = Peripheral Blood Mononuclear Cells
445
+ !Sample_organism_ch1 = Homo sapiens
446
+ !Sample_taxid_ch1 = 9606
447
+ !Sample_characteristics_ch1 = disease state: myalgic encephalomyelitis/chronic fatigue syndrome
448
+ !Sample_characteristics_ch1 = individual: Patient_One
449
+ !Sample_characteristics_ch1 = time point: E
450
+ !Sample_characteristics_ch1 = cell type: Peripheral Blood Mononuclear Cells
451
+ !Sample_molecule_ch1 = genomic DNA
452
+ !Sample_extract_protocol_ch1 = DNA was extracted from 200ul of PBMCs
453
+ !Sample_extract_protocol_ch1 = MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
454
+ !Sample_description = ME007E
455
+ !Sample_data_processing = reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
456
+ !Sample_data_processing = reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
457
+ !Sample_data_processing = bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: Chi squared test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
458
+ !Sample_data_processing = Genome_build: hg19
459
+ !Sample_data_processing = Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. C012_Full, ME007_Full and ME016_Full are excel files that contain, for the control, patient one, and patient two respectively, information about the per fragment methylation data including, genomic location, gene feature information, CpG relative location and fragment size.
460
+ !Sample_platform_id = GPL16791
461
+ !Sample_contact_name = Amber,,Helliwell
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+ !Sample_contact_department = Biochemistry Department
463
+ !Sample_contact_institute = University of Otago
464
+ !Sample_contact_address = 710 Cumberland Road
465
+ !Sample_contact_city = Dunedin
466
+ !Sample_contact_zip/postal_code = 9016
467
+ !Sample_contact_country = New Zealand
468
+ !Sample_instrument_model = Illumina HiSeq 2500
469
+ !Sample_library_selection = Reduced Representation
470
+ !Sample_library_source = genomic
471
+ !Sample_library_strategy = Bisulfite-Seq
472
+ !Sample_relation = BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN17862801
473
+ !Sample_relation = SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX10073456
474
+ !Sample_supplementary_file_1 = ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM5076nnn/GSM5076049/suppl/GSM5076049_ME007E_CpG.txt.gz
475
+ !Sample_series_id = GSE166592
476
+ !Sample_data_row_count = 0
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+ ^SAMPLE = GSM5076050
478
+ !Sample_title = Patient_Two_A
479
+ !Sample_geo_accession = GSM5076050
480
+ !Sample_status = Public on Feb 11 2021
481
+ !Sample_submission_date = Feb 10 2021
482
+ !Sample_last_update_date = Feb 12 2021
483
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484
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486
+ !Sample_organism_ch1 = Homo sapiens
487
+ !Sample_taxid_ch1 = 9606
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+ !Sample_characteristics_ch1 = disease state: myalgic encephalomyelitis/chronic fatigue syndrome
489
+ !Sample_characteristics_ch1 = individual: Patient_Two
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+ !Sample_characteristics_ch1 = time point: A
491
+ !Sample_characteristics_ch1 = cell type: Peripheral Blood Mononuclear Cells
492
+ !Sample_molecule_ch1 = genomic DNA
493
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494
+ !Sample_extract_protocol_ch1 = MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
495
+ !Sample_description = ME016A
496
+ !Sample_data_processing = reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
497
+ !Sample_data_processing = reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
498
+ !Sample_data_processing = bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: Chi squared test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
499
+ !Sample_data_processing = Genome_build: hg19
500
+ !Sample_data_processing = Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. C012_Full, ME007_Full and ME016_Full are excel files that contain, for the control, patient one, and patient two respectively, information about the per fragment methylation data including, genomic location, gene feature information, CpG relative location and fragment size.
501
+ !Sample_platform_id = GPL16791
502
+ !Sample_contact_name = Amber,,Helliwell
503
+ !Sample_contact_department = Biochemistry Department
504
+ !Sample_contact_institute = University of Otago
505
+ !Sample_contact_address = 710 Cumberland Road
506
+ !Sample_contact_city = Dunedin
507
+ !Sample_contact_zip/postal_code = 9016
508
+ !Sample_contact_country = New Zealand
509
+ !Sample_instrument_model = Illumina HiSeq 2500
510
+ !Sample_library_selection = Reduced Representation
511
+ !Sample_library_source = genomic
512
+ !Sample_library_strategy = Bisulfite-Seq
513
+ !Sample_relation = BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN17862800
514
+ !Sample_relation = SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX10073457
515
+ !Sample_supplementary_file_1 = ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM5076nnn/GSM5076050/suppl/GSM5076050_ME016A_CpG.txt.gz
516
+ !Sample_series_id = GSE166592
517
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519
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520
+ !Sample_geo_accession = GSM5076051
521
+ !Sample_status = Public on Feb 11 2021
522
+ !Sample_submission_date = Feb 10 2021
523
+ !Sample_last_update_date = Feb 12 2021
524
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525
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526
+ !Sample_source_name_ch1 = Peripheral Blood Mononuclear Cells
527
+ !Sample_organism_ch1 = Homo sapiens
528
+ !Sample_taxid_ch1 = 9606
529
+ !Sample_characteristics_ch1 = disease state: myalgic encephalomyelitis/chronic fatigue syndrome
530
+ !Sample_characteristics_ch1 = individual: Patient_Two
531
+ !Sample_characteristics_ch1 = time point: B
532
+ !Sample_characteristics_ch1 = cell type: Peripheral Blood Mononuclear Cells
533
+ !Sample_molecule_ch1 = genomic DNA
534
+ !Sample_extract_protocol_ch1 = DNA was extracted from 200ul of PBMCs
535
+ !Sample_extract_protocol_ch1 = MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
536
+ !Sample_description = ME016B
537
+ !Sample_data_processing = reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
538
+ !Sample_data_processing = reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
539
+ !Sample_data_processing = bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: Chi squared test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
540
+ !Sample_data_processing = Genome_build: hg19
541
+ !Sample_data_processing = Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. C012_Full, ME007_Full and ME016_Full are excel files that contain, for the control, patient one, and patient two respectively, information about the per fragment methylation data including, genomic location, gene feature information, CpG relative location and fragment size.
542
+ !Sample_platform_id = GPL16791
543
+ !Sample_contact_name = Amber,,Helliwell
544
+ !Sample_contact_department = Biochemistry Department
545
+ !Sample_contact_institute = University of Otago
546
+ !Sample_contact_address = 710 Cumberland Road
547
+ !Sample_contact_city = Dunedin
548
+ !Sample_contact_zip/postal_code = 9016
549
+ !Sample_contact_country = New Zealand
550
+ !Sample_instrument_model = Illumina HiSeq 2500
551
+ !Sample_library_selection = Reduced Representation
552
+ !Sample_library_source = genomic
553
+ !Sample_library_strategy = Bisulfite-Seq
554
+ !Sample_relation = BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN17862799
555
+ !Sample_relation = SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX10073458
556
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557
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558
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560
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561
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562
+ !Sample_status = Public on Feb 11 2021
563
+ !Sample_submission_date = Feb 10 2021
564
+ !Sample_last_update_date = Mar 17 2021
565
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566
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567
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568
+ !Sample_organism_ch1 = Homo sapiens
569
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570
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571
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573
+ !Sample_characteristics_ch1 = cell type: Peripheral Blood Mononuclear Cells
574
+ !Sample_molecule_ch1 = genomic DNA
575
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576
+ !Sample_extract_protocol_ch1 = MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
577
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578
+ !Sample_data_processing = reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
579
+ !Sample_data_processing = reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
580
+ !Sample_data_processing = bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: Chi squared test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
581
+ !Sample_data_processing = Genome_build: hg19
582
+ !Sample_data_processing = Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. C012_Full, ME007_Full and ME016_Full are excel files that contain, for the control, patient one, and patient two respectively, information about the per fragment methylation data including, genomic location, gene feature information, CpG relative location and fragment size.
583
+ !Sample_platform_id = GPL16791
584
+ !Sample_contact_name = Amber,,Helliwell
585
+ !Sample_contact_department = Biochemistry Department
586
+ !Sample_contact_institute = University of Otago
587
+ !Sample_contact_address = 710 Cumberland Road
588
+ !Sample_contact_city = Dunedin
589
+ !Sample_contact_zip/postal_code = 9016
590
+ !Sample_contact_country = New Zealand
591
+ !Sample_instrument_model = Illumina HiSeq 2500
592
+ !Sample_library_selection = Reduced Representation
593
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594
+ !Sample_library_strategy = Bisulfite-Seq
595
+ !Sample_relation = BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN17862798
596
+ !Sample_relation = SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX10073459
597
+ !Sample_supplementary_file_1 = ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM5076nnn/GSM5076052/suppl/GSM5076052_ME016C_CpG.txt.gz
598
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599
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600
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601
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602
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603
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604
+ !Sample_submission_date = Feb 10 2021
605
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606
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607
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608
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609
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610
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611
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612
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614
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616
+ !Sample_extract_protocol_ch1 = DNA was extracted from 200ul of PBMCs
617
+ !Sample_extract_protocol_ch1 = MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
618
+ !Sample_description = ME016D
619
+ !Sample_data_processing = reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
620
+ !Sample_data_processing = reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
621
+ !Sample_data_processing = bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: Chi squared test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
622
+ !Sample_data_processing = Genome_build: hg19
623
+ !Sample_data_processing = Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. C012_Full, ME007_Full and ME016_Full are excel files that contain, for the control, patient one, and patient two respectively, information about the per fragment methylation data including, genomic location, gene feature information, CpG relative location and fragment size.
624
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625
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626
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627
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628
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629
+ !Sample_contact_city = Dunedin
630
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632
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633
+ !Sample_library_selection = Reduced Representation
634
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635
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636
+ !Sample_relation = BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN17862797
637
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638
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639
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640
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642
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643
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644
+ !Sample_status = Public on Feb 11 2021
645
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646
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647
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655
+ !Sample_characteristics_ch1 = cell type: Peripheral Blood Mononuclear Cells
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+ !Sample_molecule_ch1 = genomic DNA
657
+ !Sample_extract_protocol_ch1 = DNA was extracted from 200ul of PBMCs
658
+ !Sample_extract_protocol_ch1 = MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
659
+ !Sample_description = ME016E
660
+ !Sample_data_processing = reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
661
+ !Sample_data_processing = reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
662
+ !Sample_data_processing = bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: Chi squared test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
663
+ !Sample_data_processing = Genome_build: hg19
664
+ !Sample_data_processing = Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. C012_Full, ME007_Full and ME016_Full are excel files that contain, for the control, patient one, and patient two respectively, information about the per fragment methylation data including, genomic location, gene feature information, CpG relative location and fragment size.
665
+ !Sample_platform_id = GPL16791
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668
+ !Sample_contact_institute = University of Otago
669
+ !Sample_contact_address = 710 Cumberland Road
670
+ !Sample_contact_city = Dunedin
671
+ !Sample_contact_zip/postal_code = 9016
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+ !Sample_contact_country = New Zealand
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+ !Sample_instrument_model = Illumina HiSeq 2500
674
+ !Sample_library_selection = Reduced Representation
675
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676
+ !Sample_library_strategy = Bisulfite-Seq
677
+ !Sample_relation = BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN17862796
678
+ !Sample_relation = SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX10073461
679
+ !Sample_supplementary_file_1 = ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM5076nnn/GSM5076054/suppl/GSM5076054_ME016E_CpG.txt.gz
680
+ !Sample_series_id = GSE166592
681
+ !Sample_data_row_count = 0
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+ <Contributor iid="contrib4">
34
+ <Person><First>Aniruddha</First><Last>Chatterjee</Last></Person>
35
+ </Contributor>
36
+
37
+ <Contributor iid="contrib5">
38
+ <Person><First>Peter</First><Last>Stockwell</Last></Person>
39
+ </Contributor>
40
+
41
+ <Contributor iid="contrib6">
42
+ <Person><First>Tina</First><Last>Edgar</Last></Person>
43
+ </Contributor>
44
+
45
+ <Database iid="GEO">
46
+ <Name>Gene Expression Omnibus (GEO)</Name>
47
+ <Public-ID>GEO</Public-ID>
48
+ <Organization>NCBI NLM NIH</Organization>
49
+ <Web-Link>http://www.ncbi.nlm.nih.gov/geo</Web-Link>
50
+ <Email>geo@ncbi.nlm.nih.gov</Email>
51
+ </Database>
52
+
53
+ <Platform iid="GPL16791">
54
+ <Status database="GEO">
55
+ <Submission-Date>2013-03-14</Submission-Date>
56
+ <Release-Date>2013-03-14</Release-Date>
57
+ <Last-Update-Date>2019-03-27</Last-Update-Date>
58
+ </Status>
59
+ <Title>Illumina HiSeq 2500 (Homo sapiens)</Title>
60
+ <Accession database="GEO">GPL16791</Accession>
61
+ <Technology>high-throughput sequencing</Technology>
62
+ <Distribution>virtual</Distribution>
63
+ <Organism taxid="9606">Homo sapiens</Organism>
64
+ <Manufacturer></Manufacturer>
65
+ <Manufacture-Protocol>
66
+ </Manufacture-Protocol>
67
+ <Contact-Ref ref="contrib2" />
68
+ </Platform>
69
+
70
+ <Sample iid="GSM5076040">
71
+ <Status database="GEO">
72
+ <Submission-Date>2021-02-10</Submission-Date>
73
+ <Release-Date>2021-02-11</Release-Date>
74
+ <Last-Update-Date>2021-02-12</Last-Update-Date>
75
+ </Status>
76
+ <Title>C012A</Title>
77
+ <Accession database="GEO">GSM5076040</Accession>
78
+ <Type>SRA</Type>
79
+ <Channel-Count>1</Channel-Count>
80
+ <Channel position="1">
81
+ <Source>Peripheral Blood Mononuclear Cells</Source>
82
+ <Organism taxid="9606">Homo sapiens</Organism>
83
+ <Characteristics tag="disease state">
84
+ Control
85
+ </Characteristics>
86
+ <Characteristics tag="individual">
87
+ C012
88
+ </Characteristics>
89
+ <Characteristics tag="time point">
90
+ A
91
+ </Characteristics>
92
+ <Characteristics tag="cell type">
93
+ Peripheral Blood Mononuclear Cells
94
+ </Characteristics>
95
+ <Molecule>genomic DNA</Molecule>
96
+ <Extract-Protocol>
97
+ DNA was extracted from 200ul of PBMCs
98
+ MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
99
+ </Extract-Protocol>
100
+ </Channel>
101
+ <Description>
102
+ C012A
103
+ </Description>
104
+ <Data-Processing>
105
+ reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
106
+ reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
107
+ bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: Chi squared test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
108
+ Genome_build: hg19
109
+ Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. C012_Full, ME007_Full and ME016_Full are excel files that contain, for the control, patient one, and patient two respectively, information about the per fragment methylation data including, genomic location, gene feature information, CpG relative location and fragment size.
110
+ </Data-Processing>
111
+ <Platform-Ref ref="GPL16791" />
112
+ <Library-Strategy>Bisulfite-Seq</Library-Strategy>
113
+ <Library-Source>genomic</Library-Source>
114
+ <Library-Selection>Reduced Representation</Library-Selection>
115
+ <Instrument-Model>
116
+ <Predefined>Illumina HiSeq 2500</Predefined>
117
+ </Instrument-Model>
118
+ <Contact-Ref ref="contrib1" />
119
+ <Supplementary-Data type="TXT">
120
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM5076nnn/GSM5076040/suppl/GSM5076040_C012A_CpG.txt.gz
121
+ </Supplementary-Data>
122
+ <Relation type="BioSample" target="https://www.ncbi.nlm.nih.gov/biosample/SAMN17862810" />
123
+ <Relation type="SRA" target="https://www.ncbi.nlm.nih.gov/sra?term=SRX10073447" />
124
+ </Sample>
125
+
126
+ <Sample iid="GSM5076041">
127
+ <Status database="GEO">
128
+ <Submission-Date>2021-02-10</Submission-Date>
129
+ <Release-Date>2021-02-11</Release-Date>
130
+ <Last-Update-Date>2021-02-12</Last-Update-Date>
131
+ </Status>
132
+ <Title>C012B</Title>
133
+ <Accession database="GEO">GSM5076041</Accession>
134
+ <Type>SRA</Type>
135
+ <Channel-Count>1</Channel-Count>
136
+ <Channel position="1">
137
+ <Source>Peripheral Blood Mononuclear Cells</Source>
138
+ <Organism taxid="9606">Homo sapiens</Organism>
139
+ <Characteristics tag="disease state">
140
+ Control
141
+ </Characteristics>
142
+ <Characteristics tag="individual">
143
+ C012
144
+ </Characteristics>
145
+ <Characteristics tag="time point">
146
+ B
147
+ </Characteristics>
148
+ <Characteristics tag="cell type">
149
+ Peripheral Blood Mononuclear Cells
150
+ </Characteristics>
151
+ <Molecule>genomic DNA</Molecule>
152
+ <Extract-Protocol>
153
+ DNA was extracted from 200ul of PBMCs
154
+ MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
155
+ </Extract-Protocol>
156
+ </Channel>
157
+ <Description>
158
+ C012B
159
+ </Description>
160
+ <Data-Processing>
161
+ reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
162
+ reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
163
+ bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: Chi squared test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
164
+ Genome_build: hg19
165
+ Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. C012_Full, ME007_Full and ME016_Full are excel files that contain, for the control, patient one, and patient two respectively, information about the per fragment methylation data including, genomic location, gene feature information, CpG relative location and fragment size.
166
+ </Data-Processing>
167
+ <Platform-Ref ref="GPL16791" />
168
+ <Library-Strategy>Bisulfite-Seq</Library-Strategy>
169
+ <Library-Source>genomic</Library-Source>
170
+ <Library-Selection>Reduced Representation</Library-Selection>
171
+ <Instrument-Model>
172
+ <Predefined>Illumina HiSeq 2500</Predefined>
173
+ </Instrument-Model>
174
+ <Contact-Ref ref="contrib1" />
175
+ <Supplementary-Data type="TXT">
176
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM5076nnn/GSM5076041/suppl/GSM5076041_C012B_CpG.txt.gz
177
+ </Supplementary-Data>
178
+ <Relation type="BioSample" target="https://www.ncbi.nlm.nih.gov/biosample/SAMN17862809" />
179
+ <Relation type="SRA" target="https://www.ncbi.nlm.nih.gov/sra?term=SRX10073448" />
180
+ </Sample>
181
+
182
+ <Sample iid="GSM5076042">
183
+ <Status database="GEO">
184
+ <Submission-Date>2021-02-10</Submission-Date>
185
+ <Release-Date>2021-02-11</Release-Date>
186
+ <Last-Update-Date>2021-02-12</Last-Update-Date>
187
+ </Status>
188
+ <Title>C012C</Title>
189
+ <Accession database="GEO">GSM5076042</Accession>
190
+ <Type>SRA</Type>
191
+ <Channel-Count>1</Channel-Count>
192
+ <Channel position="1">
193
+ <Source>Peripheral Blood Mononuclear Cells</Source>
194
+ <Organism taxid="9606">Homo sapiens</Organism>
195
+ <Characteristics tag="disease state">
196
+ Control
197
+ </Characteristics>
198
+ <Characteristics tag="individual">
199
+ C012
200
+ </Characteristics>
201
+ <Characteristics tag="time point">
202
+ C
203
+ </Characteristics>
204
+ <Characteristics tag="cell type">
205
+ Peripheral Blood Mononuclear Cells
206
+ </Characteristics>
207
+ <Molecule>genomic DNA</Molecule>
208
+ <Extract-Protocol>
209
+ DNA was extracted from 200ul of PBMCs
210
+ MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
211
+ </Extract-Protocol>
212
+ </Channel>
213
+ <Description>
214
+ C012C
215
+ </Description>
216
+ <Data-Processing>
217
+ reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
218
+ reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
219
+ bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: Chi squared test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
220
+ Genome_build: hg19
221
+ Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. C012_Full, ME007_Full and ME016_Full are excel files that contain, for the control, patient one, and patient two respectively, information about the per fragment methylation data including, genomic location, gene feature information, CpG relative location and fragment size.
222
+ </Data-Processing>
223
+ <Platform-Ref ref="GPL16791" />
224
+ <Library-Strategy>Bisulfite-Seq</Library-Strategy>
225
+ <Library-Source>genomic</Library-Source>
226
+ <Library-Selection>Reduced Representation</Library-Selection>
227
+ <Instrument-Model>
228
+ <Predefined>Illumina HiSeq 2500</Predefined>
229
+ </Instrument-Model>
230
+ <Contact-Ref ref="contrib1" />
231
+ <Supplementary-Data type="TXT">
232
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM5076nnn/GSM5076042/suppl/GSM5076042_C012C_CpG.txt.gz
233
+ </Supplementary-Data>
234
+ <Relation type="BioSample" target="https://www.ncbi.nlm.nih.gov/biosample/SAMN17862808" />
235
+ <Relation type="SRA" target="https://www.ncbi.nlm.nih.gov/sra?term=SRX10073449" />
236
+ </Sample>
237
+
238
+ <Sample iid="GSM5076043">
239
+ <Status database="GEO">
240
+ <Submission-Date>2021-02-10</Submission-Date>
241
+ <Release-Date>2021-02-11</Release-Date>
242
+ <Last-Update-Date>2021-02-12</Last-Update-Date>
243
+ </Status>
244
+ <Title>C012D</Title>
245
+ <Accession database="GEO">GSM5076043</Accession>
246
+ <Type>SRA</Type>
247
+ <Channel-Count>1</Channel-Count>
248
+ <Channel position="1">
249
+ <Source>Peripheral Blood Mononuclear Cells</Source>
250
+ <Organism taxid="9606">Homo sapiens</Organism>
251
+ <Characteristics tag="disease state">
252
+ Control
253
+ </Characteristics>
254
+ <Characteristics tag="individual">
255
+ C012
256
+ </Characteristics>
257
+ <Characteristics tag="time point">
258
+ D
259
+ </Characteristics>
260
+ <Characteristics tag="cell type">
261
+ Peripheral Blood Mononuclear Cells
262
+ </Characteristics>
263
+ <Molecule>genomic DNA</Molecule>
264
+ <Extract-Protocol>
265
+ DNA was extracted from 200ul of PBMCs
266
+ MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
267
+ </Extract-Protocol>
268
+ </Channel>
269
+ <Description>
270
+ C012D
271
+ </Description>
272
+ <Data-Processing>
273
+ reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
274
+ reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
275
+ bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: Chi squared test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
276
+ Genome_build: hg19
277
+ Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. C012_Full, ME007_Full and ME016_Full are excel files that contain, for the control, patient one, and patient two respectively, information about the per fragment methylation data including, genomic location, gene feature information, CpG relative location and fragment size.
278
+ </Data-Processing>
279
+ <Platform-Ref ref="GPL16791" />
280
+ <Library-Strategy>Bisulfite-Seq</Library-Strategy>
281
+ <Library-Source>genomic</Library-Source>
282
+ <Library-Selection>Reduced Representation</Library-Selection>
283
+ <Instrument-Model>
284
+ <Predefined>Illumina HiSeq 2500</Predefined>
285
+ </Instrument-Model>
286
+ <Contact-Ref ref="contrib1" />
287
+ <Supplementary-Data type="TXT">
288
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM5076nnn/GSM5076043/suppl/GSM5076043_C012D_CpG.txt.gz
289
+ </Supplementary-Data>
290
+ <Relation type="BioSample" target="https://www.ncbi.nlm.nih.gov/biosample/SAMN17862807" />
291
+ <Relation type="SRA" target="https://www.ncbi.nlm.nih.gov/sra?term=SRX10073450" />
292
+ </Sample>
293
+
294
+ <Sample iid="GSM5076044">
295
+ <Status database="GEO">
296
+ <Submission-Date>2021-02-10</Submission-Date>
297
+ <Release-Date>2021-02-11</Release-Date>
298
+ <Last-Update-Date>2021-02-12</Last-Update-Date>
299
+ </Status>
300
+ <Title>C012E</Title>
301
+ <Accession database="GEO">GSM5076044</Accession>
302
+ <Type>SRA</Type>
303
+ <Channel-Count>1</Channel-Count>
304
+ <Channel position="1">
305
+ <Source>Peripheral Blood Mononuclear Cells</Source>
306
+ <Organism taxid="9606">Homo sapiens</Organism>
307
+ <Characteristics tag="disease state">
308
+ Control
309
+ </Characteristics>
310
+ <Characteristics tag="individual">
311
+ C012
312
+ </Characteristics>
313
+ <Characteristics tag="time point">
314
+ E
315
+ </Characteristics>
316
+ <Characteristics tag="cell type">
317
+ Peripheral Blood Mononuclear Cells
318
+ </Characteristics>
319
+ <Molecule>genomic DNA</Molecule>
320
+ <Extract-Protocol>
321
+ DNA was extracted from 200ul of PBMCs
322
+ MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
323
+ </Extract-Protocol>
324
+ </Channel>
325
+ <Description>
326
+ C012E
327
+ </Description>
328
+ <Data-Processing>
329
+ reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
330
+ reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
331
+ bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: Chi squared test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
332
+ Genome_build: hg19
333
+ Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. C012_Full, ME007_Full and ME016_Full are excel files that contain, for the control, patient one, and patient two respectively, information about the per fragment methylation data including, genomic location, gene feature information, CpG relative location and fragment size.
334
+ </Data-Processing>
335
+ <Platform-Ref ref="GPL16791" />
336
+ <Library-Strategy>Bisulfite-Seq</Library-Strategy>
337
+ <Library-Source>genomic</Library-Source>
338
+ <Library-Selection>Reduced Representation</Library-Selection>
339
+ <Instrument-Model>
340
+ <Predefined>Illumina HiSeq 2500</Predefined>
341
+ </Instrument-Model>
342
+ <Contact-Ref ref="contrib1" />
343
+ <Supplementary-Data type="TXT">
344
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM5076nnn/GSM5076044/suppl/GSM5076044_C012E_CpG.txt.gz
345
+ </Supplementary-Data>
346
+ <Relation type="BioSample" target="https://www.ncbi.nlm.nih.gov/biosample/SAMN17862806" />
347
+ <Relation type="SRA" target="https://www.ncbi.nlm.nih.gov/sra?term=SRX10073451" />
348
+ </Sample>
349
+
350
+ <Sample iid="GSM5076045">
351
+ <Status database="GEO">
352
+ <Submission-Date>2021-02-10</Submission-Date>
353
+ <Release-Date>2021-02-11</Release-Date>
354
+ <Last-Update-Date>2021-03-17</Last-Update-Date>
355
+ </Status>
356
+ <Title>Patient_One_A</Title>
357
+ <Accession database="GEO">GSM5076045</Accession>
358
+ <Type>SRA</Type>
359
+ <Channel-Count>1</Channel-Count>
360
+ <Channel position="1">
361
+ <Source>Peripheral Blood Mononuclear Cells</Source>
362
+ <Organism taxid="9606">Homo sapiens</Organism>
363
+ <Characteristics tag="disease state">
364
+ myalgic encephalomyelitis/chronic fatigue syndrome
365
+ </Characteristics>
366
+ <Characteristics tag="individual">
367
+ Patient_One
368
+ </Characteristics>
369
+ <Characteristics tag="time point">
370
+ A
371
+ </Characteristics>
372
+ <Characteristics tag="cell type">
373
+ Peripheral Blood Mononuclear Cells
374
+ </Characteristics>
375
+ <Molecule>genomic DNA</Molecule>
376
+ <Extract-Protocol>
377
+ DNA was extracted from 200ul of PBMCs
378
+ MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
379
+ </Extract-Protocol>
380
+ </Channel>
381
+ <Description>
382
+ ME007A
383
+ </Description>
384
+ <Data-Processing>
385
+ reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
386
+ reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
387
+ bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: Chi squared test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
388
+ Genome_build: hg19
389
+ Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. C012_Full, ME007_Full and ME016_Full are excel files that contain, for the control, patient one, and patient two respectively, information about the per fragment methylation data including, genomic location, gene feature information, CpG relative location and fragment size.
390
+ </Data-Processing>
391
+ <Platform-Ref ref="GPL16791" />
392
+ <Library-Strategy>Bisulfite-Seq</Library-Strategy>
393
+ <Library-Source>genomic</Library-Source>
394
+ <Library-Selection>Reduced Representation</Library-Selection>
395
+ <Instrument-Model>
396
+ <Predefined>Illumina HiSeq 2500</Predefined>
397
+ </Instrument-Model>
398
+ <Contact-Ref ref="contrib1" />
399
+ <Supplementary-Data type="TXT">
400
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM5076nnn/GSM5076045/suppl/GSM5076045_ME007A_CpG.txt.gz
401
+ </Supplementary-Data>
402
+ <Relation type="BioSample" target="https://www.ncbi.nlm.nih.gov/biosample/SAMN17862805" />
403
+ <Relation type="SRA" target="https://www.ncbi.nlm.nih.gov/sra?term=SRX10073452" />
404
+ </Sample>
405
+
406
+ <Sample iid="GSM5076046">
407
+ <Status database="GEO">
408
+ <Submission-Date>2021-02-10</Submission-Date>
409
+ <Release-Date>2021-02-11</Release-Date>
410
+ <Last-Update-Date>2021-02-12</Last-Update-Date>
411
+ </Status>
412
+ <Title>Patient_One_B</Title>
413
+ <Accession database="GEO">GSM5076046</Accession>
414
+ <Type>SRA</Type>
415
+ <Channel-Count>1</Channel-Count>
416
+ <Channel position="1">
417
+ <Source>Peripheral Blood Mononuclear Cells</Source>
418
+ <Organism taxid="9606">Homo sapiens</Organism>
419
+ <Characteristics tag="disease state">
420
+ myalgic encephalomyelitis/chronic fatigue syndrome
421
+ </Characteristics>
422
+ <Characteristics tag="individual">
423
+ Patient_One
424
+ </Characteristics>
425
+ <Characteristics tag="time point">
426
+ B
427
+ </Characteristics>
428
+ <Characteristics tag="cell type">
429
+ Peripheral Blood Mononuclear Cells
430
+ </Characteristics>
431
+ <Molecule>genomic DNA</Molecule>
432
+ <Extract-Protocol>
433
+ DNA was extracted from 200ul of PBMCs
434
+ MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
435
+ </Extract-Protocol>
436
+ </Channel>
437
+ <Description>
438
+ ME007B
439
+ </Description>
440
+ <Data-Processing>
441
+ reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
442
+ reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
443
+ bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: Chi squared test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
444
+ Genome_build: hg19
445
+ Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. C012_Full, ME007_Full and ME016_Full are excel files that contain, for the control, patient one, and patient two respectively, information about the per fragment methylation data including, genomic location, gene feature information, CpG relative location and fragment size.
446
+ </Data-Processing>
447
+ <Platform-Ref ref="GPL16791" />
448
+ <Library-Strategy>Bisulfite-Seq</Library-Strategy>
449
+ <Library-Source>genomic</Library-Source>
450
+ <Library-Selection>Reduced Representation</Library-Selection>
451
+ <Instrument-Model>
452
+ <Predefined>Illumina HiSeq 2500</Predefined>
453
+ </Instrument-Model>
454
+ <Contact-Ref ref="contrib1" />
455
+ <Supplementary-Data type="TXT">
456
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM5076nnn/GSM5076046/suppl/GSM5076046_ME007B_CpG.txt.gz
457
+ </Supplementary-Data>
458
+ <Relation type="BioSample" target="https://www.ncbi.nlm.nih.gov/biosample/SAMN17862804" />
459
+ <Relation type="SRA" target="https://www.ncbi.nlm.nih.gov/sra?term=SRX10073453" />
460
+ </Sample>
461
+
462
+ <Sample iid="GSM5076047">
463
+ <Status database="GEO">
464
+ <Submission-Date>2021-02-10</Submission-Date>
465
+ <Release-Date>2021-02-11</Release-Date>
466
+ <Last-Update-Date>2021-02-12</Last-Update-Date>
467
+ </Status>
468
+ <Title>Patient_One_C</Title>
469
+ <Accession database="GEO">GSM5076047</Accession>
470
+ <Type>SRA</Type>
471
+ <Channel-Count>1</Channel-Count>
472
+ <Channel position="1">
473
+ <Source>Peripheral Blood Mononuclear Cells</Source>
474
+ <Organism taxid="9606">Homo sapiens</Organism>
475
+ <Characteristics tag="disease state">
476
+ myalgic encephalomyelitis/chronic fatigue syndrome
477
+ </Characteristics>
478
+ <Characteristics tag="individual">
479
+ Patient_One
480
+ </Characteristics>
481
+ <Characteristics tag="time point">
482
+ C
483
+ </Characteristics>
484
+ <Characteristics tag="cell type">
485
+ Peripheral Blood Mononuclear Cells
486
+ </Characteristics>
487
+ <Molecule>genomic DNA</Molecule>
488
+ <Extract-Protocol>
489
+ DNA was extracted from 200ul of PBMCs
490
+ MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
491
+ </Extract-Protocol>
492
+ </Channel>
493
+ <Description>
494
+ ME007C
495
+ </Description>
496
+ <Data-Processing>
497
+ reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
498
+ reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
499
+ bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: Chi squared test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
500
+ Genome_build: hg19
501
+ Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. C012_Full, ME007_Full and ME016_Full are excel files that contain, for the control, patient one, and patient two respectively, information about the per fragment methylation data including, genomic location, gene feature information, CpG relative location and fragment size.
502
+ </Data-Processing>
503
+ <Platform-Ref ref="GPL16791" />
504
+ <Library-Strategy>Bisulfite-Seq</Library-Strategy>
505
+ <Library-Source>genomic</Library-Source>
506
+ <Library-Selection>Reduced Representation</Library-Selection>
507
+ <Instrument-Model>
508
+ <Predefined>Illumina HiSeq 2500</Predefined>
509
+ </Instrument-Model>
510
+ <Contact-Ref ref="contrib1" />
511
+ <Supplementary-Data type="TXT">
512
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM5076nnn/GSM5076047/suppl/GSM5076047_ME007C_CpG.txt.gz
513
+ </Supplementary-Data>
514
+ <Relation type="BioSample" target="https://www.ncbi.nlm.nih.gov/biosample/SAMN17862803" />
515
+ <Relation type="SRA" target="https://www.ncbi.nlm.nih.gov/sra?term=SRX10073454" />
516
+ </Sample>
517
+
518
+ <Sample iid="GSM5076048">
519
+ <Status database="GEO">
520
+ <Submission-Date>2021-02-10</Submission-Date>
521
+ <Release-Date>2021-02-11</Release-Date>
522
+ <Last-Update-Date>2021-02-12</Last-Update-Date>
523
+ </Status>
524
+ <Title>Patient_One_D</Title>
525
+ <Accession database="GEO">GSM5076048</Accession>
526
+ <Type>SRA</Type>
527
+ <Channel-Count>1</Channel-Count>
528
+ <Channel position="1">
529
+ <Source>Peripheral Blood Mononuclear Cells</Source>
530
+ <Organism taxid="9606">Homo sapiens</Organism>
531
+ <Characteristics tag="disease state">
532
+ myalgic encephalomyelitis/chronic fatigue syndrome
533
+ </Characteristics>
534
+ <Characteristics tag="individual">
535
+ Patient_One
536
+ </Characteristics>
537
+ <Characteristics tag="time point">
538
+ D
539
+ </Characteristics>
540
+ <Characteristics tag="cell type">
541
+ Peripheral Blood Mononuclear Cells
542
+ </Characteristics>
543
+ <Molecule>genomic DNA</Molecule>
544
+ <Extract-Protocol>
545
+ DNA was extracted from 200ul of PBMCs
546
+ MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
547
+ </Extract-Protocol>
548
+ </Channel>
549
+ <Description>
550
+ ME007D
551
+ </Description>
552
+ <Data-Processing>
553
+ reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
554
+ reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
555
+ bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: Chi squared test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
556
+ Genome_build: hg19
557
+ Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. C012_Full, ME007_Full and ME016_Full are excel files that contain, for the control, patient one, and patient two respectively, information about the per fragment methylation data including, genomic location, gene feature information, CpG relative location and fragment size.
558
+ </Data-Processing>
559
+ <Platform-Ref ref="GPL16791" />
560
+ <Library-Strategy>Bisulfite-Seq</Library-Strategy>
561
+ <Library-Source>genomic</Library-Source>
562
+ <Library-Selection>Reduced Representation</Library-Selection>
563
+ <Instrument-Model>
564
+ <Predefined>Illumina HiSeq 2500</Predefined>
565
+ </Instrument-Model>
566
+ <Contact-Ref ref="contrib1" />
567
+ <Supplementary-Data type="TXT">
568
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM5076nnn/GSM5076048/suppl/GSM5076048_ME007D_CpG.txt.gz
569
+ </Supplementary-Data>
570
+ <Relation type="BioSample" target="https://www.ncbi.nlm.nih.gov/biosample/SAMN17862802" />
571
+ <Relation type="SRA" target="https://www.ncbi.nlm.nih.gov/sra?term=SRX10073455" />
572
+ </Sample>
573
+
574
+ <Sample iid="GSM5076049">
575
+ <Status database="GEO">
576
+ <Submission-Date>2021-02-10</Submission-Date>
577
+ <Release-Date>2021-02-11</Release-Date>
578
+ <Last-Update-Date>2021-02-12</Last-Update-Date>
579
+ </Status>
580
+ <Title>Patient_One_E</Title>
581
+ <Accession database="GEO">GSM5076049</Accession>
582
+ <Type>SRA</Type>
583
+ <Channel-Count>1</Channel-Count>
584
+ <Channel position="1">
585
+ <Source>Peripheral Blood Mononuclear Cells</Source>
586
+ <Organism taxid="9606">Homo sapiens</Organism>
587
+ <Characteristics tag="disease state">
588
+ myalgic encephalomyelitis/chronic fatigue syndrome
589
+ </Characteristics>
590
+ <Characteristics tag="individual">
591
+ Patient_One
592
+ </Characteristics>
593
+ <Characteristics tag="time point">
594
+ E
595
+ </Characteristics>
596
+ <Characteristics tag="cell type">
597
+ Peripheral Blood Mononuclear Cells
598
+ </Characteristics>
599
+ <Molecule>genomic DNA</Molecule>
600
+ <Extract-Protocol>
601
+ DNA was extracted from 200ul of PBMCs
602
+ MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
603
+ </Extract-Protocol>
604
+ </Channel>
605
+ <Description>
606
+ ME007E
607
+ </Description>
608
+ <Data-Processing>
609
+ reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
610
+ reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
611
+ bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: Chi squared test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
612
+ Genome_build: hg19
613
+ Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. C012_Full, ME007_Full and ME016_Full are excel files that contain, for the control, patient one, and patient two respectively, information about the per fragment methylation data including, genomic location, gene feature information, CpG relative location and fragment size.
614
+ </Data-Processing>
615
+ <Platform-Ref ref="GPL16791" />
616
+ <Library-Strategy>Bisulfite-Seq</Library-Strategy>
617
+ <Library-Source>genomic</Library-Source>
618
+ <Library-Selection>Reduced Representation</Library-Selection>
619
+ <Instrument-Model>
620
+ <Predefined>Illumina HiSeq 2500</Predefined>
621
+ </Instrument-Model>
622
+ <Contact-Ref ref="contrib1" />
623
+ <Supplementary-Data type="TXT">
624
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM5076nnn/GSM5076049/suppl/GSM5076049_ME007E_CpG.txt.gz
625
+ </Supplementary-Data>
626
+ <Relation type="BioSample" target="https://www.ncbi.nlm.nih.gov/biosample/SAMN17862801" />
627
+ <Relation type="SRA" target="https://www.ncbi.nlm.nih.gov/sra?term=SRX10073456" />
628
+ </Sample>
629
+
630
+ <Sample iid="GSM5076050">
631
+ <Status database="GEO">
632
+ <Submission-Date>2021-02-10</Submission-Date>
633
+ <Release-Date>2021-02-11</Release-Date>
634
+ <Last-Update-Date>2021-02-12</Last-Update-Date>
635
+ </Status>
636
+ <Title>Patient_Two_A</Title>
637
+ <Accession database="GEO">GSM5076050</Accession>
638
+ <Type>SRA</Type>
639
+ <Channel-Count>1</Channel-Count>
640
+ <Channel position="1">
641
+ <Source>Peripheral Blood Mononuclear Cells</Source>
642
+ <Organism taxid="9606">Homo sapiens</Organism>
643
+ <Characteristics tag="disease state">
644
+ myalgic encephalomyelitis/chronic fatigue syndrome
645
+ </Characteristics>
646
+ <Characteristics tag="individual">
647
+ Patient_Two
648
+ </Characteristics>
649
+ <Characteristics tag="time point">
650
+ A
651
+ </Characteristics>
652
+ <Characteristics tag="cell type">
653
+ Peripheral Blood Mononuclear Cells
654
+ </Characteristics>
655
+ <Molecule>genomic DNA</Molecule>
656
+ <Extract-Protocol>
657
+ DNA was extracted from 200ul of PBMCs
658
+ MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
659
+ </Extract-Protocol>
660
+ </Channel>
661
+ <Description>
662
+ ME016A
663
+ </Description>
664
+ <Data-Processing>
665
+ reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
666
+ reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
667
+ bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: Chi squared test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
668
+ Genome_build: hg19
669
+ Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. C012_Full, ME007_Full and ME016_Full are excel files that contain, for the control, patient one, and patient two respectively, information about the per fragment methylation data including, genomic location, gene feature information, CpG relative location and fragment size.
670
+ </Data-Processing>
671
+ <Platform-Ref ref="GPL16791" />
672
+ <Library-Strategy>Bisulfite-Seq</Library-Strategy>
673
+ <Library-Source>genomic</Library-Source>
674
+ <Library-Selection>Reduced Representation</Library-Selection>
675
+ <Instrument-Model>
676
+ <Predefined>Illumina HiSeq 2500</Predefined>
677
+ </Instrument-Model>
678
+ <Contact-Ref ref="contrib1" />
679
+ <Supplementary-Data type="TXT">
680
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM5076nnn/GSM5076050/suppl/GSM5076050_ME016A_CpG.txt.gz
681
+ </Supplementary-Data>
682
+ <Relation type="BioSample" target="https://www.ncbi.nlm.nih.gov/biosample/SAMN17862800" />
683
+ <Relation type="SRA" target="https://www.ncbi.nlm.nih.gov/sra?term=SRX10073457" />
684
+ </Sample>
685
+
686
+ <Sample iid="GSM5076051">
687
+ <Status database="GEO">
688
+ <Submission-Date>2021-02-10</Submission-Date>
689
+ <Release-Date>2021-02-11</Release-Date>
690
+ <Last-Update-Date>2021-02-12</Last-Update-Date>
691
+ </Status>
692
+ <Title>Patient_Two_B</Title>
693
+ <Accession database="GEO">GSM5076051</Accession>
694
+ <Type>SRA</Type>
695
+ <Channel-Count>1</Channel-Count>
696
+ <Channel position="1">
697
+ <Source>Peripheral Blood Mononuclear Cells</Source>
698
+ <Organism taxid="9606">Homo sapiens</Organism>
699
+ <Characteristics tag="disease state">
700
+ myalgic encephalomyelitis/chronic fatigue syndrome
701
+ </Characteristics>
702
+ <Characteristics tag="individual">
703
+ Patient_Two
704
+ </Characteristics>
705
+ <Characteristics tag="time point">
706
+ B
707
+ </Characteristics>
708
+ <Characteristics tag="cell type">
709
+ Peripheral Blood Mononuclear Cells
710
+ </Characteristics>
711
+ <Molecule>genomic DNA</Molecule>
712
+ <Extract-Protocol>
713
+ DNA was extracted from 200ul of PBMCs
714
+ MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
715
+ </Extract-Protocol>
716
+ </Channel>
717
+ <Description>
718
+ ME016B
719
+ </Description>
720
+ <Data-Processing>
721
+ reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
722
+ reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
723
+ bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: Chi squared test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
724
+ Genome_build: hg19
725
+ Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. C012_Full, ME007_Full and ME016_Full are excel files that contain, for the control, patient one, and patient two respectively, information about the per fragment methylation data including, genomic location, gene feature information, CpG relative location and fragment size.
726
+ </Data-Processing>
727
+ <Platform-Ref ref="GPL16791" />
728
+ <Library-Strategy>Bisulfite-Seq</Library-Strategy>
729
+ <Library-Source>genomic</Library-Source>
730
+ <Library-Selection>Reduced Representation</Library-Selection>
731
+ <Instrument-Model>
732
+ <Predefined>Illumina HiSeq 2500</Predefined>
733
+ </Instrument-Model>
734
+ <Contact-Ref ref="contrib1" />
735
+ <Supplementary-Data type="TXT">
736
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM5076nnn/GSM5076051/suppl/GSM5076051_ME016B_CpG.txt.gz
737
+ </Supplementary-Data>
738
+ <Relation type="BioSample" target="https://www.ncbi.nlm.nih.gov/biosample/SAMN17862799" />
739
+ <Relation type="SRA" target="https://www.ncbi.nlm.nih.gov/sra?term=SRX10073458" />
740
+ </Sample>
741
+
742
+ <Sample iid="GSM5076052">
743
+ <Status database="GEO">
744
+ <Submission-Date>2021-02-10</Submission-Date>
745
+ <Release-Date>2021-02-11</Release-Date>
746
+ <Last-Update-Date>2021-03-17</Last-Update-Date>
747
+ </Status>
748
+ <Title>Patient_Two_C</Title>
749
+ <Accession database="GEO">GSM5076052</Accession>
750
+ <Type>SRA</Type>
751
+ <Channel-Count>1</Channel-Count>
752
+ <Channel position="1">
753
+ <Source>Peripheral Blood Mononuclear Cells</Source>
754
+ <Organism taxid="9606">Homo sapiens</Organism>
755
+ <Characteristics tag="disease state">
756
+ myalgic encephalomyelitis/chronic fatigue syndrome
757
+ </Characteristics>
758
+ <Characteristics tag="individual">
759
+ Patient_Two
760
+ </Characteristics>
761
+ <Characteristics tag="time point">
762
+ C
763
+ </Characteristics>
764
+ <Characteristics tag="cell type">
765
+ Peripheral Blood Mononuclear Cells
766
+ </Characteristics>
767
+ <Molecule>genomic DNA</Molecule>
768
+ <Extract-Protocol>
769
+ DNA was extracted from 200ul of PBMCs
770
+ MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
771
+ </Extract-Protocol>
772
+ </Channel>
773
+ <Description>
774
+ ME016C
775
+ </Description>
776
+ <Data-Processing>
777
+ reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
778
+ reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
779
+ bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: Chi squared test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
780
+ Genome_build: hg19
781
+ Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. C012_Full, ME007_Full and ME016_Full are excel files that contain, for the control, patient one, and patient two respectively, information about the per fragment methylation data including, genomic location, gene feature information, CpG relative location and fragment size.
782
+ </Data-Processing>
783
+ <Platform-Ref ref="GPL16791" />
784
+ <Library-Strategy>Bisulfite-Seq</Library-Strategy>
785
+ <Library-Source>genomic</Library-Source>
786
+ <Library-Selection>Reduced Representation</Library-Selection>
787
+ <Instrument-Model>
788
+ <Predefined>Illumina HiSeq 2500</Predefined>
789
+ </Instrument-Model>
790
+ <Contact-Ref ref="contrib1" />
791
+ <Supplementary-Data type="TXT">
792
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM5076nnn/GSM5076052/suppl/GSM5076052_ME016C_CpG.txt.gz
793
+ </Supplementary-Data>
794
+ <Relation type="BioSample" target="https://www.ncbi.nlm.nih.gov/biosample/SAMN17862798" />
795
+ <Relation type="SRA" target="https://www.ncbi.nlm.nih.gov/sra?term=SRX10073459" />
796
+ </Sample>
797
+
798
+ <Sample iid="GSM5076053">
799
+ <Status database="GEO">
800
+ <Submission-Date>2021-02-10</Submission-Date>
801
+ <Release-Date>2021-02-11</Release-Date>
802
+ <Last-Update-Date>2021-02-12</Last-Update-Date>
803
+ </Status>
804
+ <Title>Patient_Two_D</Title>
805
+ <Accession database="GEO">GSM5076053</Accession>
806
+ <Type>SRA</Type>
807
+ <Channel-Count>1</Channel-Count>
808
+ <Channel position="1">
809
+ <Source>Peripheral Blood Mononuclear Cells</Source>
810
+ <Organism taxid="9606">Homo sapiens</Organism>
811
+ <Characteristics tag="disease state">
812
+ myalgic encephalomyelitis/chronic fatigue syndrome
813
+ </Characteristics>
814
+ <Characteristics tag="individual">
815
+ Patient_Two
816
+ </Characteristics>
817
+ <Characteristics tag="time point">
818
+ D
819
+ </Characteristics>
820
+ <Characteristics tag="cell type">
821
+ Peripheral Blood Mononuclear Cells
822
+ </Characteristics>
823
+ <Molecule>genomic DNA</Molecule>
824
+ <Extract-Protocol>
825
+ DNA was extracted from 200ul of PBMCs
826
+ MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
827
+ </Extract-Protocol>
828
+ </Channel>
829
+ <Description>
830
+ ME016D
831
+ </Description>
832
+ <Data-Processing>
833
+ reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
834
+ reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
835
+ bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: Chi squared test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
836
+ Genome_build: hg19
837
+ Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. C012_Full, ME007_Full and ME016_Full are excel files that contain, for the control, patient one, and patient two respectively, information about the per fragment methylation data including, genomic location, gene feature information, CpG relative location and fragment size.
838
+ </Data-Processing>
839
+ <Platform-Ref ref="GPL16791" />
840
+ <Library-Strategy>Bisulfite-Seq</Library-Strategy>
841
+ <Library-Source>genomic</Library-Source>
842
+ <Library-Selection>Reduced Representation</Library-Selection>
843
+ <Instrument-Model>
844
+ <Predefined>Illumina HiSeq 2500</Predefined>
845
+ </Instrument-Model>
846
+ <Contact-Ref ref="contrib1" />
847
+ <Supplementary-Data type="TXT">
848
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM5076nnn/GSM5076053/suppl/GSM5076053_ME016D_CpG.txt.gz
849
+ </Supplementary-Data>
850
+ <Relation type="BioSample" target="https://www.ncbi.nlm.nih.gov/biosample/SAMN17862797" />
851
+ <Relation type="SRA" target="https://www.ncbi.nlm.nih.gov/sra?term=SRX10073460" />
852
+ </Sample>
853
+
854
+ <Sample iid="GSM5076054">
855
+ <Status database="GEO">
856
+ <Submission-Date>2021-02-10</Submission-Date>
857
+ <Release-Date>2021-02-11</Release-Date>
858
+ <Last-Update-Date>2021-02-12</Last-Update-Date>
859
+ </Status>
860
+ <Title>Patient_Two_E</Title>
861
+ <Accession database="GEO">GSM5076054</Accession>
862
+ <Type>SRA</Type>
863
+ <Channel-Count>1</Channel-Count>
864
+ <Channel position="1">
865
+ <Source>Peripheral Blood Mononuclear Cells</Source>
866
+ <Organism taxid="9606">Homo sapiens</Organism>
867
+ <Characteristics tag="disease state">
868
+ myalgic encephalomyelitis/chronic fatigue syndrome
869
+ </Characteristics>
870
+ <Characteristics tag="individual">
871
+ Patient_Two
872
+ </Characteristics>
873
+ <Characteristics tag="time point">
874
+ E
875
+ </Characteristics>
876
+ <Characteristics tag="cell type">
877
+ Peripheral Blood Mononuclear Cells
878
+ </Characteristics>
879
+ <Molecule>genomic DNA</Molecule>
880
+ <Extract-Protocol>
881
+ DNA was extracted from 200ul of PBMCs
882
+ MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)
883
+ </Extract-Protocol>
884
+ </Channel>
885
+ <Description>
886
+ ME016E
887
+ </Description>
888
+ <Data-Processing>
889
+ reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp
890
+ reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible
891
+ bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: Chi squared test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data.
892
+ Genome_build: hg19
893
+ Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. C012_Full, ME007_Full and ME016_Full are excel files that contain, for the control, patient one, and patient two respectively, information about the per fragment methylation data including, genomic location, gene feature information, CpG relative location and fragment size.
894
+ </Data-Processing>
895
+ <Platform-Ref ref="GPL16791" />
896
+ <Library-Strategy>Bisulfite-Seq</Library-Strategy>
897
+ <Library-Source>genomic</Library-Source>
898
+ <Library-Selection>Reduced Representation</Library-Selection>
899
+ <Instrument-Model>
900
+ <Predefined>Illumina HiSeq 2500</Predefined>
901
+ </Instrument-Model>
902
+ <Contact-Ref ref="contrib1" />
903
+ <Supplementary-Data type="TXT">
904
+ ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM5076nnn/GSM5076054/suppl/GSM5076054_ME016E_CpG.txt.gz
905
+ </Supplementary-Data>
906
+ <Relation type="BioSample" target="https://www.ncbi.nlm.nih.gov/biosample/SAMN17862796" />
907
+ <Relation type="SRA" target="https://www.ncbi.nlm.nih.gov/sra?term=SRX10073461" />
908
+ </Sample>
909
+
910
+ <Series iid="GSE166592">
911
+ <Status database="GEO">
912
+ <Submission-Date>2021-02-10</Submission-Date>
913
+ <Release-Date>2021-02-11</Release-Date>
914
+ <Last-Update-Date>2021-03-17</Last-Update-Date>
915
+ </Status>
916
+ <Title>Dynamic Epigenetic Changes during a Relapse and Recovery Cycle in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome </Title>
917
+ <Accession database="GEO">GSE166592</Accession>
918
+ <Summary>
919
+ Purpose: ME/CFS is a debilitating and complex disease. The majority of patients exist in a chronic state of health where they are affected by relapse events. Precision medicine following patients can capture changes in the DNA methylation indicative of biological dysfunction
920
+ Methods: DNA was extracted from the PBMCs of 2 ME/CFS patients and a age/gender matched control at five different time points. After performing RRBS the sequence was aligned to hg19 genome using Bismark. The data was analyzed using a Chi squared test through DMAP in order to determine variation between the patient and control groups across 40-220bp fragments of the genome.
921
+ Results: A total of 17 and 14 statistically significant variably methylated fragements were indentified in each patient that strongly associated with a relapse event. These fragements were found on regions of regulatory importance of the genome that associated with immune (primarily inflammatory) and metabolic function.
922
+ Conclusions: Our study represents the first investigation of ME/CFS patients using reduced representation bisulfite sequencing along a longitudinal timeframe. We captured a number of major variably methylated fragments in each patient that associated with their relapse events. Our results identified a number of differentially methylated regulatory elements and gene bodies that highlight the disturbed pathophysiology in ME/CFS. DNA methylation that differentiates disease variability in ongoing ME/CFS may have practical applications for strategies to deacrease the frequency and severity of relapse events.
923
+ </Summary>
924
+ <Overall-Design>
925
+ RRBS Analysis of 2 ME/CFS patients and matched control over eleven months
926
+ </Overall-Design>
927
+ <Type>Methylation profiling by high throughput sequencing</Type>
928
+ <Contributor-Ref ref="contrib1" position="1" />
929
+ <Contributor-Ref ref="contrib3" position="2" />
930
+ <Contributor-Ref ref="contrib4" position="3" />
931
+ <Contributor-Ref ref="contrib5" position="4" />
932
+ <Contributor-Ref ref="contrib6" position="5" />
933
+ <Contact-Ref ref="contrib1" />
934
+ <Sample-Ref ref="GSM5076040" />
935
+ <Sample-Ref ref="GSM5076041" />
936
+ <Sample-Ref ref="GSM5076042" />
937
+ <Sample-Ref ref="GSM5076043" />
938
+ <Sample-Ref ref="GSM5076044" />
939
+ <Sample-Ref ref="GSM5076045" />
940
+ <Sample-Ref ref="GSM5076046" />
941
+ <Sample-Ref ref="GSM5076047" />
942
+ <Sample-Ref ref="GSM5076048" />
943
+ <Sample-Ref ref="GSM5076049" />
944
+ <Sample-Ref ref="GSM5076050" />
945
+ <Sample-Ref ref="GSM5076051" />
946
+ <Sample-Ref ref="GSM5076052" />
947
+ <Sample-Ref ref="GSM5076053" />
948
+ <Sample-Ref ref="GSM5076054" />
949
+ <Supplementary-Data type="XLSX">
950
+ ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE166nnn/GSE166592/suppl/GSE166592_C012_Full.xlsx
951
+ </Supplementary-Data>
952
+ <Supplementary-Data type="XLSX">
953
+ ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE166nnn/GSE166592/suppl/GSE166592_ME007_Full.xlsx
954
+ </Supplementary-Data>
955
+ <Supplementary-Data type="XLSX">
956
+ ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE166nnn/GSE166592/suppl/GSE166592_ME016_Full.xlsx
957
+ </Supplementary-Data>
958
+ <Supplementary-Data type="TAR">
959
+ ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE166nnn/GSE166592/suppl/GSE166592_RAW.tar
960
+ </Supplementary-Data>
961
+ <Relation type="BioProject" target="https://www.ncbi.nlm.nih.gov/bioproject/PRJNA701322" />
962
+ <Relation type="SRA" target="https://www.ncbi.nlm.nih.gov/sra?term=SRP305748" />
963
+ </Series>
964
+
965
+ </MINiML>
ME/GSE166592/meta/GSE166592_series_matrix.txt ADDED
@@ -0,0 +1,76 @@
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
1
+ !Series_title "Dynamic Epigenetic Changes during a Relapse and Recovery Cycle in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome "
2
+ !Series_geo_accession "GSE166592"
3
+ !Series_status "Public on Feb 11 2021"
4
+ !Series_submission_date "Feb 10 2021"
5
+ !Series_last_update_date "Mar 17 2021"
6
+ !Series_summary "Purpose: ME/CFS is a debilitating and complex disease. The majority of patients exist in a chronic state of health where they are affected by relapse events. Precision medicine following patients can capture changes in the DNA methylation indicative of biological dysfunction"
7
+ !Series_summary "Methods: DNA was extracted from the PBMCs of 2 ME/CFS patients and a age/gender matched control at five different time points. After performing RRBS the sequence was aligned to hg19 genome using Bismark. The data was analyzed using a Chi squared test through DMAP in order to determine variation between the patient and control groups across 40-220bp fragments of the genome."
8
+ !Series_summary "Results: A total of 17 and 14 statistically significant variably methylated fragements were indentified in each patient that strongly associated with a relapse event. These fragements were found on regions of regulatory importance of the genome that associated with immune (primarily inflammatory) and metabolic function."
9
+ !Series_summary "Conclusions: Our study represents the first investigation of ME/CFS patients using reduced representation bisulfite sequencing along a longitudinal timeframe. We captured a number of major variably methylated fragments in each patient that associated with their relapse events. Our results identified a number of differentially methylated regulatory elements and gene bodies that highlight the disturbed pathophysiology in ME/CFS. DNA methylation that differentiates disease variability in ongoing ME/CFS may have practical applications for strategies to deacrease the frequency and severity of relapse events."
10
+ !Series_overall_design "RRBS Analysis of 2 ME/CFS patients and matched control over eleven months"
11
+ !Series_type "Methylation profiling by high throughput sequencing"
12
+ !Series_contributor "Amber,,Helliwell"
13
+ !Series_contributor "Warren,,Tate"
14
+ !Series_contributor "Aniruddha,,Chatterjee"
15
+ !Series_contributor "Peter,,Stockwell"
16
+ !Series_contributor "Tina,,Edgar"
17
+ !Series_sample_id "GSM5076040 GSM5076041 GSM5076042 GSM5076043 GSM5076044 GSM5076045 GSM5076046 GSM5076047 GSM5076048 GSM5076049 GSM5076050 GSM5076051 GSM5076052 GSM5076053 GSM5076054 "
18
+ !Series_contact_name "Amber,,Helliwell"
19
+ !Series_contact_department "Biochemistry Department"
20
+ !Series_contact_institute "University of Otago"
21
+ !Series_contact_address "710 Cumberland Road"
22
+ !Series_contact_city "Dunedin"
23
+ !Series_contact_zip/postal_code "9016"
24
+ !Series_contact_country "New Zealand"
25
+ !Series_supplementary_file "ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE166nnn/GSE166592/suppl/GSE166592_C012_Full.xlsx"
26
+ !Series_supplementary_file "ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE166nnn/GSE166592/suppl/GSE166592_ME007_Full.xlsx"
27
+ !Series_supplementary_file "ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE166nnn/GSE166592/suppl/GSE166592_ME016_Full.xlsx"
28
+ !Series_supplementary_file "ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE166nnn/GSE166592/suppl/GSE166592_RAW.tar"
29
+ !Series_platform_id "GPL16791"
30
+ !Series_platform_taxid "9606"
31
+ !Series_sample_taxid "9606"
32
+ !Series_relation "BioProject: https://www.ncbi.nlm.nih.gov/bioproject/PRJNA701322"
33
+ !Series_relation "SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRP305748"
34
+
35
+ !Sample_title "C012A" "C012B" "C012C" "C012D" "C012E" "Patient_One_A" "Patient_One_B" "Patient_One_C" "Patient_One_D" "Patient_One_E" "Patient_Two_A" "Patient_Two_B" "Patient_Two_C" "Patient_Two_D" "Patient_Two_E"
36
+ !Sample_geo_accession "GSM5076040" "GSM5076041" "GSM5076042" "GSM5076043" "GSM5076044" "GSM5076045" "GSM5076046" "GSM5076047" "GSM5076048" "GSM5076049" "GSM5076050" "GSM5076051" "GSM5076052" "GSM5076053" "GSM5076054"
37
+ !Sample_status "Public on Feb 11 2021" "Public on Feb 11 2021" "Public on Feb 11 2021" "Public on Feb 11 2021" "Public on Feb 11 2021" "Public on Feb 11 2021" "Public on Feb 11 2021" "Public on Feb 11 2021" "Public on Feb 11 2021" "Public on Feb 11 2021" "Public on Feb 11 2021" "Public on Feb 11 2021" "Public on Feb 11 2021" "Public on Feb 11 2021" "Public on Feb 11 2021"
38
+ !Sample_submission_date "Feb 10 2021" "Feb 10 2021" "Feb 10 2021" "Feb 10 2021" "Feb 10 2021" "Feb 10 2021" "Feb 10 2021" "Feb 10 2021" "Feb 10 2021" "Feb 10 2021" "Feb 10 2021" "Feb 10 2021" "Feb 10 2021" "Feb 10 2021" "Feb 10 2021"
39
+ !Sample_last_update_date "Feb 12 2021" "Feb 12 2021" "Feb 12 2021" "Feb 12 2021" "Feb 12 2021" "Mar 17 2021" "Feb 12 2021" "Feb 12 2021" "Feb 12 2021" "Feb 12 2021" "Feb 12 2021" "Feb 12 2021" "Mar 17 2021" "Feb 12 2021" "Feb 12 2021"
40
+ !Sample_type "SRA" "SRA" "SRA" "SRA" "SRA" "SRA" "SRA" "SRA" "SRA" "SRA" "SRA" "SRA" "SRA" "SRA" "SRA"
41
+ !Sample_channel_count "1" "1" "1" "1" "1" "1" "1" "1" "1" "1" "1" "1" "1" "1" "1"
42
+ !Sample_source_name_ch1 "Peripheral Blood Mononuclear Cells" "Peripheral Blood Mononuclear Cells" "Peripheral Blood Mononuclear Cells" "Peripheral Blood Mononuclear Cells" "Peripheral Blood Mononuclear Cells" "Peripheral Blood Mononuclear Cells" "Peripheral Blood Mononuclear Cells" "Peripheral Blood Mononuclear Cells" "Peripheral Blood Mononuclear Cells" "Peripheral Blood Mononuclear Cells" "Peripheral Blood Mononuclear Cells" "Peripheral Blood Mononuclear Cells" "Peripheral Blood Mononuclear Cells" "Peripheral Blood Mononuclear Cells" "Peripheral Blood Mononuclear Cells"
43
+ !Sample_organism_ch1 "Homo sapiens" "Homo sapiens" "Homo sapiens" "Homo sapiens" "Homo sapiens" "Homo sapiens" "Homo sapiens" "Homo sapiens" "Homo sapiens" "Homo sapiens" "Homo sapiens" "Homo sapiens" "Homo sapiens" "Homo sapiens" "Homo sapiens"
44
+ !Sample_characteristics_ch1 "disease state: Control" "disease state: Control" "disease state: Control" "disease state: Control" "disease state: Control" "disease state: myalgic encephalomyelitis/chronic fatigue syndrome" "disease state: myalgic encephalomyelitis/chronic fatigue syndrome" "disease state: myalgic encephalomyelitis/chronic fatigue syndrome" "disease state: myalgic encephalomyelitis/chronic fatigue syndrome" "disease state: myalgic encephalomyelitis/chronic fatigue syndrome" "disease state: myalgic encephalomyelitis/chronic fatigue syndrome" "disease state: myalgic encephalomyelitis/chronic fatigue syndrome" "disease state: myalgic encephalomyelitis/chronic fatigue syndrome" "disease state: myalgic encephalomyelitis/chronic fatigue syndrome" "disease state: myalgic encephalomyelitis/chronic fatigue syndrome"
45
+ !Sample_characteristics_ch1 "individual: C012" "individual: C012" "individual: C012" "individual: C012" "individual: C012" "individual: Patient_One" "individual: Patient_One" "individual: Patient_One" "individual: Patient_One" "individual: Patient_One" "individual: Patient_Two" "individual: Patient_Two" "individual: Patient_Two" "individual: Patient_Two" "individual: Patient_Two"
46
+ !Sample_characteristics_ch1 "time point: A" "time point: B" "time point: C" "time point: D" "time point: E" "time point: A" "time point: B" "time point: C" "time point: D" "time point: E" "time point: A" "time point: B" "time point: C" "time point: D" "time point: E"
47
+ !Sample_characteristics_ch1 "cell type: Peripheral Blood Mononuclear Cells" "cell type: Peripheral Blood Mononuclear Cells" "cell type: Peripheral Blood Mononuclear Cells" "cell type: Peripheral Blood Mononuclear Cells" "cell type: Peripheral Blood Mononuclear Cells" "cell type: Peripheral Blood Mononuclear Cells" "cell type: Peripheral Blood Mononuclear Cells" "cell type: Peripheral Blood Mononuclear Cells" "cell type: Peripheral Blood Mononuclear Cells" "cell type: Peripheral Blood Mononuclear Cells" "cell type: Peripheral Blood Mononuclear Cells" "cell type: Peripheral Blood Mononuclear Cells" "cell type: Peripheral Blood Mononuclear Cells" "cell type: Peripheral Blood Mononuclear Cells" "cell type: Peripheral Blood Mononuclear Cells"
48
+ !Sample_molecule_ch1 "genomic DNA" "genomic DNA" "genomic DNA" "genomic DNA" "genomic DNA" "genomic DNA" "genomic DNA" "genomic DNA" "genomic DNA" "genomic DNA" "genomic DNA" "genomic DNA" "genomic DNA" "genomic DNA" "genomic DNA"
49
+ !Sample_extract_protocol_ch1 "DNA was extracted from 200ul of PBMCs" "DNA was extracted from 200ul of PBMCs" "DNA was extracted from 200ul of PBMCs" "DNA was extracted from 200ul of PBMCs" "DNA was extracted from 200ul of PBMCs" "DNA was extracted from 200ul of PBMCs" "DNA was extracted from 200ul of PBMCs" "DNA was extracted from 200ul of PBMCs" "DNA was extracted from 200ul of PBMCs" "DNA was extracted from 200ul of PBMCs" "DNA was extracted from 200ul of PBMCs" "DNA was extracted from 200ul of PBMCs" "DNA was extracted from 200ul of PBMCs" "DNA was extracted from 200ul of PBMCs" "DNA was extracted from 200ul of PBMCs"
50
+ !Sample_extract_protocol_ch1 "MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)" "MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)" "MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)" "MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)" "MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)" "MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)" "MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)" "MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)" "MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)" "MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)" "MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)" "MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)" "MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)" "MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)" "MSPI digestion (purify), end repair (purify), A-tialing and adaptor ligation (purify), PCR amplification (purify), Gel size selection and gel extraction (purify)"
51
+ !Sample_taxid_ch1 "9606" "9606" "9606" "9606" "9606" "9606" "9606" "9606" "9606" "9606" "9606" "9606" "9606" "9606" "9606"
52
+ !Sample_description "C012A" "C012B" "C012C" "C012D" "C012E" "ME007A" "ME007B" "ME007C" "ME007D" "ME007E" "ME016A" "ME016B" "ME016C" "ME016D" "ME016E"
53
+ !Sample_data_processing "reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp" "reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp" "reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp" "reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp" "reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp" "reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp" "reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp" "reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp" "reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp" "reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp" "reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp" "reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp" "reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp" "reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp" "reads were adaptor trimmed using bismark that used a file of adaptor sequences and trimmed three bases back from any detected adaptor to delete the C invorporated and rejecting any reads that were trimmed to less than 10bp"
54
+ !Sample_data_processing "reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible" "reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible" "reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible" "reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible" "reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible" "reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible" "reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible" "reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible" "reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible" "reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible" "reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible" "reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible" "reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible" "reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible" "reads were aligned to the hg19 genome using bismark with the following specifications: a tolerance for one non-bisulfite mismatch per read, the default minimum alignment score (L,O, -02), and with ignore - quals in order to calculate the mismatch penalty by considering the quality value at the mismatched position to be the highest possible"
55
+ !Sample_data_processing "bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: Chi squared test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data." "bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: Chi squared test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data." "bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: Chi squared test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data." "bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: Chi squared test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data." "bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: Chi squared test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data." "bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: Chi squared test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data." "bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: Chi squared test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data." "bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: Chi squared test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data." "bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: Chi squared test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data." "bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: Chi squared test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data." "bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: Chi squared test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data." "bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: Chi squared test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data." "bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: Chi squared test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data." "bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: Chi squared test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data." "bam files generated by Bismark alignment were then processed using DMAP to compare control vs. patients with the following specifications: Chi squared test on fragments 40-220bp in length, with the fragment requireing at lest 2 CpGs to have 10 or more sequence reads. The differential methylation file was then annotated with protein coding gene information using the DMAP command identgeneloc. DMAPmatrix.csv file contains this data."
56
+ !Sample_data_processing "Genome_build: hg19" "Genome_build: hg19" "Genome_build: hg19" "Genome_build: hg19" "Genome_build: hg19" "Genome_build: hg19" "Genome_build: hg19" "Genome_build: hg19" "Genome_build: hg19" "Genome_build: hg19" "Genome_build: hg19" "Genome_build: hg19" "Genome_build: hg19" "Genome_build: hg19" "Genome_build: hg19"
57
+ !Sample_data_processing "Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. C012_Full, ME007_Full and ME016_Full are excel files that contain, for the control, patient one, and patient two respectively, information about the per fragment methylation data including, genomic location, gene feature information, CpG relative location and fragment size." "Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. C012_Full, ME007_Full and ME016_Full are excel files that contain, for the control, patient one, and patient two respectively, information about the per fragment methylation data including, genomic location, gene feature information, CpG relative location and fragment size." "Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. C012_Full, ME007_Full and ME016_Full are excel files that contain, for the control, patient one, and patient two respectively, information about the per fragment methylation data including, genomic location, gene feature information, CpG relative location and fragment size." "Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. C012_Full, ME007_Full and ME016_Full are excel files that contain, for the control, patient one, and patient two respectively, information about the per fragment methylation data including, genomic location, gene feature information, CpG relative location and fragment size." "Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. C012_Full, ME007_Full and ME016_Full are excel files that contain, for the control, patient one, and patient two respectively, information about the per fragment methylation data including, genomic location, gene feature information, CpG relative location and fragment size." "Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. C012_Full, ME007_Full and ME016_Full are excel files that contain, for the control, patient one, and patient two respectively, information about the per fragment methylation data including, genomic location, gene feature information, CpG relative location and fragment size." "Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. C012_Full, ME007_Full and ME016_Full are excel files that contain, for the control, patient one, and patient two respectively, information about the per fragment methylation data including, genomic location, gene feature information, CpG relative location and fragment size." "Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. C012_Full, ME007_Full and ME016_Full are excel files that contain, for the control, patient one, and patient two respectively, information about the per fragment methylation data including, genomic location, gene feature information, CpG relative location and fragment size." "Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. C012_Full, ME007_Full and ME016_Full are excel files that contain, for the control, patient one, and patient two respectively, information about the per fragment methylation data including, genomic location, gene feature information, CpG relative location and fragment size." "Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. C012_Full, ME007_Full and ME016_Full are excel files that contain, for the control, patient one, and patient two respectively, information about the per fragment methylation data including, genomic location, gene feature information, CpG relative location and fragment size." "Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. C012_Full, ME007_Full and ME016_Full are excel files that contain, for the control, patient one, and patient two respectively, information about the per fragment methylation data including, genomic location, gene feature information, CpG relative location and fragment size." "Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. C012_Full, ME007_Full and ME016_Full are excel files that contain, for the control, patient one, and patient two respectively, information about the per fragment methylation data including, genomic location, gene feature information, CpG relative location and fragment size." "Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. C012_Full, ME007_Full and ME016_Full are excel files that contain, for the control, patient one, and patient two respectively, information about the per fragment methylation data including, genomic location, gene feature information, CpG relative location and fragment size." "Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. C012_Full, ME007_Full and ME016_Full are excel files that contain, for the control, patient one, and patient two respectively, information about the per fragment methylation data including, genomic location, gene feature information, CpG relative location and fragment size." "Supplementary_files_format_and_content: Individual .txt files for each sample containing C and T frequency per base and coverage. C012_Full, ME007_Full and ME016_Full are excel files that contain, for the control, patient one, and patient two respectively, information about the per fragment methylation data including, genomic location, gene feature information, CpG relative location and fragment size."
58
+ !Sample_platform_id "GPL16791" "GPL16791" "GPL16791" "GPL16791" "GPL16791" "GPL16791" "GPL16791" "GPL16791" "GPL16791" "GPL16791" "GPL16791" "GPL16791" "GPL16791" "GPL16791" "GPL16791"
59
+ !Sample_contact_name "Amber,,Helliwell" "Amber,,Helliwell" "Amber,,Helliwell" "Amber,,Helliwell" "Amber,,Helliwell" "Amber,,Helliwell" "Amber,,Helliwell" "Amber,,Helliwell" "Amber,,Helliwell" "Amber,,Helliwell" "Amber,,Helliwell" "Amber,,Helliwell" "Amber,,Helliwell" "Amber,,Helliwell" "Amber,,Helliwell"
60
+ !Sample_contact_department "Biochemistry Department" "Biochemistry Department" "Biochemistry Department" "Biochemistry Department" "Biochemistry Department" "Biochemistry Department" "Biochemistry Department" "Biochemistry Department" "Biochemistry Department" "Biochemistry Department" "Biochemistry Department" "Biochemistry Department" "Biochemistry Department" "Biochemistry Department" "Biochemistry Department"
61
+ !Sample_contact_institute "University of Otago" "University of Otago" "University of Otago" "University of Otago" "University of Otago" "University of Otago" "University of Otago" "University of Otago" "University of Otago" "University of Otago" "University of Otago" "University of Otago" "University of Otago" "University of Otago" "University of Otago"
62
+ !Sample_contact_address "710 Cumberland Road" "710 Cumberland Road" "710 Cumberland Road" "710 Cumberland Road" "710 Cumberland Road" "710 Cumberland Road" "710 Cumberland Road" "710 Cumberland Road" "710 Cumberland Road" "710 Cumberland Road" "710 Cumberland Road" "710 Cumberland Road" "710 Cumberland Road" "710 Cumberland Road" "710 Cumberland Road"
63
+ !Sample_contact_city "Dunedin" "Dunedin" "Dunedin" "Dunedin" "Dunedin" "Dunedin" "Dunedin" "Dunedin" "Dunedin" "Dunedin" "Dunedin" "Dunedin" "Dunedin" "Dunedin" "Dunedin"
64
+ !Sample_contact_zip/postal_code "9016" "9016" "9016" "9016" "9016" "9016" "9016" "9016" "9016" "9016" "9016" "9016" "9016" "9016" "9016"
65
+ !Sample_contact_country "New Zealand" "New Zealand" "New Zealand" "New Zealand" "New Zealand" "New Zealand" "New Zealand" "New Zealand" "New Zealand" "New Zealand" "New Zealand" "New Zealand" "New Zealand" "New Zealand" "New Zealand"
66
+ !Sample_data_row_count "0" "0" "0" "0" "0" "0" "0" "0" "0" "0" "0" "0" "0" "0" "0"
67
+ !Sample_instrument_model "Illumina HiSeq 2500" "Illumina HiSeq 2500" "Illumina HiSeq 2500" "Illumina HiSeq 2500" "Illumina HiSeq 2500" "Illumina HiSeq 2500" "Illumina HiSeq 2500" "Illumina HiSeq 2500" "Illumina HiSeq 2500" "Illumina HiSeq 2500" "Illumina HiSeq 2500" "Illumina HiSeq 2500" "Illumina HiSeq 2500" "Illumina HiSeq 2500" "Illumina HiSeq 2500"
68
+ !Sample_library_selection "Reduced Representation" "Reduced Representation" "Reduced Representation" "Reduced Representation" "Reduced Representation" "Reduced Representation" "Reduced Representation" "Reduced Representation" "Reduced Representation" "Reduced Representation" "Reduced Representation" "Reduced Representation" "Reduced Representation" "Reduced Representation" "Reduced Representation"
69
+ !Sample_library_source "genomic" "genomic" "genomic" "genomic" "genomic" "genomic" "genomic" "genomic" "genomic" "genomic" "genomic" "genomic" "genomic" "genomic" "genomic"
70
+ !Sample_library_strategy "Bisulfite-Seq" "Bisulfite-Seq" "Bisulfite-Seq" "Bisulfite-Seq" "Bisulfite-Seq" "Bisulfite-Seq" "Bisulfite-Seq" "Bisulfite-Seq" "Bisulfite-Seq" "Bisulfite-Seq" "Bisulfite-Seq" "Bisulfite-Seq" "Bisulfite-Seq" "Bisulfite-Seq" "Bisulfite-Seq"
71
+ !Sample_relation "BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN17862810" "BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN17862809" "BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN17862808" "BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN17862807" "BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN17862806" "BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN17862805" "BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN17862804" "BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN17862803" "BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN17862802" "BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN17862801" "BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN17862800" "BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN17862799" "BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN17862798" "BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN17862797" "BioSample: https://www.ncbi.nlm.nih.gov/biosample/SAMN17862796"
72
+ !Sample_relation "SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX10073447" "SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX10073448" "SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX10073449" "SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX10073450" "SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX10073451" "SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX10073452" "SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX10073453" "SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX10073454" "SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX10073455" "SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX10073456" "SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX10073457" "SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX10073458" "SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX10073459" "SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX10073460" "SRA: https://www.ncbi.nlm.nih.gov/sra?term=SRX10073461"
73
+ !Sample_supplementary_file_1 "ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM5076nnn/GSM5076040/suppl/GSM5076040_C012A_CpG.txt.gz" "ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM5076nnn/GSM5076041/suppl/GSM5076041_C012B_CpG.txt.gz" "ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM5076nnn/GSM5076042/suppl/GSM5076042_C012C_CpG.txt.gz" "ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM5076nnn/GSM5076043/suppl/GSM5076043_C012D_CpG.txt.gz" "ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM5076nnn/GSM5076044/suppl/GSM5076044_C012E_CpG.txt.gz" "ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM5076nnn/GSM5076045/suppl/GSM5076045_ME007A_CpG.txt.gz" "ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM5076nnn/GSM5076046/suppl/GSM5076046_ME007B_CpG.txt.gz" "ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM5076nnn/GSM5076047/suppl/GSM5076047_ME007C_CpG.txt.gz" "ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM5076nnn/GSM5076048/suppl/GSM5076048_ME007D_CpG.txt.gz" "ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM5076nnn/GSM5076049/suppl/GSM5076049_ME007E_CpG.txt.gz" "ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM5076nnn/GSM5076050/suppl/GSM5076050_ME016A_CpG.txt.gz" "ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM5076nnn/GSM5076051/suppl/GSM5076051_ME016B_CpG.txt.gz" "ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM5076nnn/GSM5076052/suppl/GSM5076052_ME016C_CpG.txt.gz" "ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM5076nnn/GSM5076053/suppl/GSM5076053_ME016D_CpG.txt.gz" "ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM5076nnn/GSM5076054/suppl/GSM5076054_ME016E_CpG.txt.gz"
74
+ !series_matrix_table_begin
75
+ "ID_REF" "GSM5076040" "GSM5076041" "GSM5076042" "GSM5076043" "GSM5076044" "GSM5076045" "GSM5076046" "GSM5076047" "GSM5076048" "GSM5076049" "GSM5076050" "GSM5076051" "GSM5076052" "GSM5076053" "GSM5076054"
76
+ !series_matrix_table_end
ME/GSE59489/GSE59489_RAW/GPL13534_450K_Manifest_header_Descriptions.xlsx ADDED
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+ <Channel-Count>1</Channel-Count>
434
+ <Channel position="1">
435
+ <Source>CFS PBMC</Source>
436
+ <Organism taxid="9606">Homo sapiens</Organism>
437
+ <Characteristics tag="gender">
438
+ female
439
+ </Characteristics>
440
+ <Characteristics tag="subject id">
441
+ CFS subject 4
442
+ </Characteristics>
443
+ <Characteristics tag="disease state">
444
+ Chronic Fatigue Syndrome (CFS)
445
+ </Characteristics>
446
+ <Characteristics tag="cell type">
447
+ peripheral blood mononuclear cells (PBMC)
448
+ </Characteristics>
449
+ <Molecule>genomic DNA</Molecule>
450
+ <Extract-Protocol>
451
+ Omega EZNA Tissue DNA Kit; Qiagen MinElute Reaction Cleanup Kit; Genome Quebec sample processing protocols
452
+ </Extract-Protocol>
453
+ <Label>Cy3,Cy5</Label>
454
+ <Label-Protocol>
455
+ Standard Illumina Protocol
456
+ </Label-Protocol>
457
+ </Channel>
458
+ <Hybridization-Protocol>
459
+ Standard Illumina Protocol
460
+ </Hybridization-Protocol>
461
+ <Scan-Protocol>
462
+ Standard Illumina Protocol
463
+ </Scan-Protocol>
464
+ <Description>
465
+ PBMC genomic DNA from CFS subject 4
466
+ 7985#WG0153568-DNA#A04#G00042
467
+ </Description>
468
+ <Data-Processing>
469
+ Illumina Genome Studio; the non_normalized.txt contains unmethylated (A) and methylated (B) signal intensities.
470
+ </Data-Processing>
471
+ <Platform-Ref ref="GPL13534" />
472
+ <Contact-Ref ref="contrib1" />
473
+ <Supplementary-Data type="unknown">
474
+ NONE
475
+ </Supplementary-Data>
476
+ <Data-Table>
477
+ <Column position="1">
478
+ <Name>ID_REF</Name>
479
+ </Column>
480
+ <Column position="2">
481
+ <Name>VALUE</Name>
482
+ <Description>Average Beta</Description>
483
+ </Column>
484
+ <Column position="3">
485
+ <Name>Detection Pval</Name>
486
+ </Column>
487
+ <External-Data rows="485577">
488
+ GSM1437762-tbl-1.txt
489
+ </External-Data>
490
+ </Data-Table>
491
+ </Sample>
492
+
493
+ <Sample iid="GSM1437763">
494
+ <Status database="GEO">
495
+ <Submission-Date>2014-07-16</Submission-Date>
496
+ <Release-Date>2014-08-12</Release-Date>
497
+ <Last-Update-Date>2014-08-12</Last-Update-Date>
498
+ </Status>
499
+ <Title>PBMC genomic DNA_CFS5</Title>
500
+ <Accession database="GEO">GSM1437763</Accession>
501
+ <Type>genomic</Type>
502
+ <Channel-Count>1</Channel-Count>
503
+ <Channel position="1">
504
+ <Source>CFS PBMC</Source>
505
+ <Organism taxid="9606">Homo sapiens</Organism>
506
+ <Characteristics tag="gender">
507
+ female
508
+ </Characteristics>
509
+ <Characteristics tag="subject id">
510
+ CFS subject 5
511
+ </Characteristics>
512
+ <Characteristics tag="disease state">
513
+ Chronic Fatigue Syndrome (CFS)
514
+ </Characteristics>
515
+ <Characteristics tag="cell type">
516
+ peripheral blood mononuclear cells (PBMC)
517
+ </Characteristics>
518
+ <Molecule>genomic DNA</Molecule>
519
+ <Extract-Protocol>
520
+ Omega EZNA Tissue DNA Kit; Qiagen MinElute Reaction Cleanup Kit; Genome Quebec sample processing protocols
521
+ </Extract-Protocol>
522
+ <Label>Cy3,Cy5</Label>
523
+ <Label-Protocol>
524
+ Standard Illumina Protocol
525
+ </Label-Protocol>
526
+ </Channel>
527
+ <Hybridization-Protocol>
528
+ Standard Illumina Protocol
529
+ </Hybridization-Protocol>
530
+ <Scan-Protocol>
531
+ Standard Illumina Protocol
532
+ </Scan-Protocol>
533
+ <Description>
534
+ PBMC genomic DNA from CFS subject 5
535
+ 7985#WG0153568-DNA#A05#G00080
536
+ </Description>
537
+ <Data-Processing>
538
+ Illumina Genome Studio; the non_normalized.txt contains unmethylated (A) and methylated (B) signal intensities.
539
+ </Data-Processing>
540
+ <Platform-Ref ref="GPL13534" />
541
+ <Contact-Ref ref="contrib1" />
542
+ <Supplementary-Data type="unknown">
543
+ NONE
544
+ </Supplementary-Data>
545
+ <Data-Table>
546
+ <Column position="1">
547
+ <Name>ID_REF</Name>
548
+ </Column>
549
+ <Column position="2">
550
+ <Name>VALUE</Name>
551
+ <Description>Average Beta</Description>
552
+ </Column>
553
+ <Column position="3">
554
+ <Name>Detection Pval</Name>
555
+ </Column>
556
+ <External-Data rows="485577">
557
+ GSM1437763-tbl-1.txt
558
+ </External-Data>
559
+ </Data-Table>
560
+ </Sample>
561
+
562
+ <Sample iid="GSM1437764">
563
+ <Status database="GEO">
564
+ <Submission-Date>2014-07-16</Submission-Date>
565
+ <Release-Date>2014-08-12</Release-Date>
566
+ <Last-Update-Date>2014-08-12</Last-Update-Date>
567
+ </Status>
568
+ <Title>PBMC genomic DNA_CFS6</Title>
569
+ <Accession database="GEO">GSM1437764</Accession>
570
+ <Type>genomic</Type>
571
+ <Channel-Count>1</Channel-Count>
572
+ <Channel position="1">
573
+ <Source>CFS PBMC</Source>
574
+ <Organism taxid="9606">Homo sapiens</Organism>
575
+ <Characteristics tag="gender">
576
+ female
577
+ </Characteristics>
578
+ <Characteristics tag="subject id">
579
+ CFS subject 6
580
+ </Characteristics>
581
+ <Characteristics tag="disease state">
582
+ Chronic Fatigue Syndrome (CFS)
583
+ </Characteristics>
584
+ <Characteristics tag="cell type">
585
+ peripheral blood mononuclear cells (PBMC)
586
+ </Characteristics>
587
+ <Molecule>genomic DNA</Molecule>
588
+ <Extract-Protocol>
589
+ Omega EZNA Tissue DNA Kit; Qiagen MinElute Reaction Cleanup Kit; Genome Quebec sample processing protocols
590
+ </Extract-Protocol>
591
+ <Label>Cy3,Cy5</Label>
592
+ <Label-Protocol>
593
+ Standard Illumina Protocol
594
+ </Label-Protocol>
595
+ </Channel>
596
+ <Hybridization-Protocol>
597
+ Standard Illumina Protocol
598
+ </Hybridization-Protocol>
599
+ <Scan-Protocol>
600
+ Standard Illumina Protocol
601
+ </Scan-Protocol>
602
+ <Description>
603
+ PBMC genomic DNA from CFS subject 6
604
+ 7985#WG0153568-DNA#A06#G00200
605
+ </Description>
606
+ <Data-Processing>
607
+ Illumina Genome Studio; the non_normalized.txt contains unmethylated (A) and methylated (B) signal intensities.
608
+ </Data-Processing>
609
+ <Platform-Ref ref="GPL13534" />
610
+ <Contact-Ref ref="contrib1" />
611
+ <Supplementary-Data type="unknown">
612
+ NONE
613
+ </Supplementary-Data>
614
+ <Data-Table>
615
+ <Column position="1">
616
+ <Name>ID_REF</Name>
617
+ </Column>
618
+ <Column position="2">
619
+ <Name>VALUE</Name>
620
+ <Description>Average Beta</Description>
621
+ </Column>
622
+ <Column position="3">
623
+ <Name>Detection Pval</Name>
624
+ </Column>
625
+ <External-Data rows="485577">
626
+ GSM1437764-tbl-1.txt
627
+ </External-Data>
628
+ </Data-Table>
629
+ </Sample>
630
+
631
+ <Sample iid="GSM1437765">
632
+ <Status database="GEO">
633
+ <Submission-Date>2014-07-16</Submission-Date>
634
+ <Release-Date>2014-08-12</Release-Date>
635
+ <Last-Update-Date>2014-08-12</Last-Update-Date>
636
+ </Status>
637
+ <Title>PBMC genomic DNA_Control1</Title>
638
+ <Accession database="GEO">GSM1437765</Accession>
639
+ <Type>genomic</Type>
640
+ <Channel-Count>1</Channel-Count>
641
+ <Channel position="1">
642
+ <Source>Control PBMC</Source>
643
+ <Organism taxid="9606">Homo sapiens</Organism>
644
+ <Characteristics tag="gender">
645
+ female
646
+ </Characteristics>
647
+ <Characteristics tag="subject id">
648
+ Control subject 1
649
+ </Characteristics>
650
+ <Characteristics tag="disease state">
651
+ Control
652
+ </Characteristics>
653
+ <Characteristics tag="cell type">
654
+ peripheral blood mononuclear cells (PBMC)
655
+ </Characteristics>
656
+ <Molecule>genomic DNA</Molecule>
657
+ <Extract-Protocol>
658
+ Omega EZNA Tissue DNA Kit; Qiagen MinElute Reaction Cleanup Kit; Genome Quebec sample processing protocols
659
+ </Extract-Protocol>
660
+ <Label>Cy3,Cy5</Label>
661
+ <Label-Protocol>
662
+ Standard Illumina Protocol
663
+ </Label-Protocol>
664
+ </Channel>
665
+ <Hybridization-Protocol>
666
+ Standard Illumina Protocol
667
+ </Hybridization-Protocol>
668
+ <Scan-Protocol>
669
+ Standard Illumina Protocol
670
+ </Scan-Protocol>
671
+ <Description>
672
+ PBMC genomic DNA from Control subject 1
673
+ 7985#WG0153568-DNA#A07#G00211
674
+ </Description>
675
+ <Data-Processing>
676
+ Illumina Genome Studio; the non_normalized.txt contains unmethylated (A) and methylated (B) signal intensities.
677
+ </Data-Processing>
678
+ <Platform-Ref ref="GPL13534" />
679
+ <Contact-Ref ref="contrib1" />
680
+ <Supplementary-Data type="unknown">
681
+ NONE
682
+ </Supplementary-Data>
683
+ <Data-Table>
684
+ <Column position="1">
685
+ <Name>ID_REF</Name>
686
+ </Column>
687
+ <Column position="2">
688
+ <Name>VALUE</Name>
689
+ <Description>Average Beta</Description>
690
+ </Column>
691
+ <Column position="3">
692
+ <Name>Detection Pval</Name>
693
+ </Column>
694
+ <External-Data rows="485577">
695
+ GSM1437765-tbl-1.txt
696
+ </External-Data>
697
+ </Data-Table>
698
+ </Sample>
699
+
700
+ <Sample iid="GSM1437766">
701
+ <Status database="GEO">
702
+ <Submission-Date>2014-07-16</Submission-Date>
703
+ <Release-Date>2014-08-12</Release-Date>
704
+ <Last-Update-Date>2014-08-12</Last-Update-Date>
705
+ </Status>
706
+ <Title>PBMC genomic DNA_Control2</Title>
707
+ <Accession database="GEO">GSM1437766</Accession>
708
+ <Type>genomic</Type>
709
+ <Channel-Count>1</Channel-Count>
710
+ <Channel position="1">
711
+ <Source>Control PBMC</Source>
712
+ <Organism taxid="9606">Homo sapiens</Organism>
713
+ <Characteristics tag="gender">
714
+ female
715
+ </Characteristics>
716
+ <Characteristics tag="subject id">
717
+ Control subject 2
718
+ </Characteristics>
719
+ <Characteristics tag="disease state">
720
+ Control
721
+ </Characteristics>
722
+ <Characteristics tag="cell type">
723
+ peripheral blood mononuclear cells (PBMC)
724
+ </Characteristics>
725
+ <Molecule>genomic DNA</Molecule>
726
+ <Extract-Protocol>
727
+ Omega EZNA Tissue DNA Kit; Qiagen MinElute Reaction Cleanup Kit; Genome Quebec sample processing protocols
728
+ </Extract-Protocol>
729
+ <Label>Cy3,Cy5</Label>
730
+ <Label-Protocol>
731
+ Standard Illumina Protocol
732
+ </Label-Protocol>
733
+ </Channel>
734
+ <Hybridization-Protocol>
735
+ Standard Illumina Protocol
736
+ </Hybridization-Protocol>
737
+ <Scan-Protocol>
738
+ Standard Illumina Protocol
739
+ </Scan-Protocol>
740
+ <Description>
741
+ PBMC genomic DNA from Control subject 2
742
+ 7985#WG0153568-DNA#A08#G00140
743
+ </Description>
744
+ <Data-Processing>
745
+ Illumina Genome Studio; the non_normalized.txt contains unmethylated (A) and methylated (B) signal intensities.
746
+ </Data-Processing>
747
+ <Platform-Ref ref="GPL13534" />
748
+ <Contact-Ref ref="contrib1" />
749
+ <Supplementary-Data type="unknown">
750
+ NONE
751
+ </Supplementary-Data>
752
+ <Data-Table>
753
+ <Column position="1">
754
+ <Name>ID_REF</Name>
755
+ </Column>
756
+ <Column position="2">
757
+ <Name>VALUE</Name>
758
+ <Description>Average Beta</Description>
759
+ </Column>
760
+ <Column position="3">
761
+ <Name>Detection Pval</Name>
762
+ </Column>
763
+ <External-Data rows="485577">
764
+ GSM1437766-tbl-1.txt
765
+ </External-Data>
766
+ </Data-Table>
767
+ </Sample>
768
+
769
+ <Sample iid="GSM1437767">
770
+ <Status database="GEO">
771
+ <Submission-Date>2014-07-16</Submission-Date>
772
+ <Release-Date>2014-08-12</Release-Date>
773
+ <Last-Update-Date>2014-08-12</Last-Update-Date>
774
+ </Status>
775
+ <Title>PBMC genomic DNA_Control3</Title>
776
+ <Accession database="GEO">GSM1437767</Accession>
777
+ <Type>genomic</Type>
778
+ <Channel-Count>1</Channel-Count>
779
+ <Channel position="1">
780
+ <Source>Control PBMC</Source>
781
+ <Organism taxid="9606">Homo sapiens</Organism>
782
+ <Characteristics tag="gender">
783
+ female
784
+ </Characteristics>
785
+ <Characteristics tag="subject id">
786
+ Control subject 3
787
+ </Characteristics>
788
+ <Characteristics tag="disease state">
789
+ Control
790
+ </Characteristics>
791
+ <Characteristics tag="cell type">
792
+ peripheral blood mononuclear cells (PBMC)
793
+ </Characteristics>
794
+ <Molecule>genomic DNA</Molecule>
795
+ <Extract-Protocol>
796
+ Omega EZNA Tissue DNA Kit; Qiagen MinElute Reaction Cleanup Kit; Genome Quebec sample processing protocols
797
+ </Extract-Protocol>
798
+ <Label>Cy3,Cy5</Label>
799
+ <Label-Protocol>
800
+ Standard Illumina Protocol
801
+ </Label-Protocol>
802
+ </Channel>
803
+ <Hybridization-Protocol>
804
+ Standard Illumina Protocol
805
+ </Hybridization-Protocol>
806
+ <Scan-Protocol>
807
+ Standard Illumina Protocol
808
+ </Scan-Protocol>
809
+ <Description>
810
+ PBMC genomic DNA from Control subject 3
811
+ 7985#WG0153568-DNA#A09#G00158
812
+ </Description>
813
+ <Data-Processing>
814
+ Illumina Genome Studio; the non_normalized.txt contains unmethylated (A) and methylated (B) signal intensities.
815
+ </Data-Processing>
816
+ <Platform-Ref ref="GPL13534" />
817
+ <Contact-Ref ref="contrib1" />
818
+ <Supplementary-Data type="unknown">
819
+ NONE
820
+ </Supplementary-Data>
821
+ <Data-Table>
822
+ <Column position="1">
823
+ <Name>ID_REF</Name>
824
+ </Column>
825
+ <Column position="2">
826
+ <Name>VALUE</Name>
827
+ <Description>Average Beta</Description>
828
+ </Column>
829
+ <Column position="3">
830
+ <Name>Detection Pval</Name>
831
+ </Column>
832
+ <External-Data rows="485577">
833
+ GSM1437767-tbl-1.txt
834
+ </External-Data>
835
+ </Data-Table>
836
+ </Sample>
837
+
838
+ <Sample iid="GSM1437768">
839
+ <Status database="GEO">
840
+ <Submission-Date>2014-07-16</Submission-Date>
841
+ <Release-Date>2014-08-12</Release-Date>
842
+ <Last-Update-Date>2014-08-12</Last-Update-Date>
843
+ </Status>
844
+ <Title>PBMC genomic DNA_Control4</Title>
845
+ <Accession database="GEO">GSM1437768</Accession>
846
+ <Type>genomic</Type>
847
+ <Channel-Count>1</Channel-Count>
848
+ <Channel position="1">
849
+ <Source>Control PBMC</Source>
850
+ <Organism taxid="9606">Homo sapiens</Organism>
851
+ <Characteristics tag="gender">
852
+ female
853
+ </Characteristics>
854
+ <Characteristics tag="subject id">
855
+ Control subject 4
856
+ </Characteristics>
857
+ <Characteristics tag="disease state">
858
+ Control
859
+ </Characteristics>
860
+ <Characteristics tag="cell type">
861
+ peripheral blood mononuclear cells (PBMC)
862
+ </Characteristics>
863
+ <Molecule>genomic DNA</Molecule>
864
+ <Extract-Protocol>
865
+ Omega EZNA Tissue DNA Kit; Qiagen MinElute Reaction Cleanup Kit; Genome Quebec sample processing protocols
866
+ </Extract-Protocol>
867
+ <Label>Cy3,Cy5</Label>
868
+ <Label-Protocol>
869
+ Standard Illumina Protocol
870
+ </Label-Protocol>
871
+ </Channel>
872
+ <Hybridization-Protocol>
873
+ Standard Illumina Protocol
874
+ </Hybridization-Protocol>
875
+ <Scan-Protocol>
876
+ Standard Illumina Protocol
877
+ </Scan-Protocol>
878
+ <Description>
879
+ PBMC genomic DNA from Control subject 4
880
+ 7985#WG0153568-DNA#A10#G00212
881
+ </Description>
882
+ <Data-Processing>
883
+ Illumina Genome Studio; the non_normalized.txt contains unmethylated (A) and methylated (B) signal intensities.
884
+ </Data-Processing>
885
+ <Platform-Ref ref="GPL13534" />
886
+ <Contact-Ref ref="contrib1" />
887
+ <Supplementary-Data type="unknown">
888
+ NONE
889
+ </Supplementary-Data>
890
+ <Data-Table>
891
+ <Column position="1">
892
+ <Name>ID_REF</Name>
893
+ </Column>
894
+ <Column position="2">
895
+ <Name>VALUE</Name>
896
+ <Description>Average Beta</Description>
897
+ </Column>
898
+ <Column position="3">
899
+ <Name>Detection Pval</Name>
900
+ </Column>
901
+ <External-Data rows="485577">
902
+ GSM1437768-tbl-1.txt
903
+ </External-Data>
904
+ </Data-Table>
905
+ </Sample>
906
+
907
+ <Sample iid="GSM1437769">
908
+ <Status database="GEO">
909
+ <Submission-Date>2014-07-16</Submission-Date>
910
+ <Release-Date>2014-08-12</Release-Date>
911
+ <Last-Update-Date>2014-08-12</Last-Update-Date>
912
+ </Status>
913
+ <Title>PBMC genomic DNA_Control5</Title>
914
+ <Accession database="GEO">GSM1437769</Accession>
915
+ <Type>genomic</Type>
916
+ <Channel-Count>1</Channel-Count>
917
+ <Channel position="1">
918
+ <Source>Control PBMC</Source>
919
+ <Organism taxid="9606">Homo sapiens</Organism>
920
+ <Characteristics tag="gender">
921
+ female
922
+ </Characteristics>
923
+ <Characteristics tag="subject id">
924
+ Control subject 5
925
+ </Characteristics>
926
+ <Characteristics tag="disease state">
927
+ Control
928
+ </Characteristics>
929
+ <Characteristics tag="cell type">
930
+ peripheral blood mononuclear cells (PBMC)
931
+ </Characteristics>
932
+ <Molecule>genomic DNA</Molecule>
933
+ <Extract-Protocol>
934
+ Omega EZNA Tissue DNA Kit; Qiagen MinElute Reaction Cleanup Kit; Genome Quebec sample processing protocols
935
+ </Extract-Protocol>
936
+ <Label>Cy3,Cy5</Label>
937
+ <Label-Protocol>
938
+ Standard Illumina Protocol
939
+ </Label-Protocol>
940
+ </Channel>
941
+ <Hybridization-Protocol>
942
+ Standard Illumina Protocol
943
+ </Hybridization-Protocol>
944
+ <Scan-Protocol>
945
+ Standard Illumina Protocol
946
+ </Scan-Protocol>
947
+ <Description>
948
+ PBMC genomic DNA from Control subject 5
949
+ 7985#WG0153568-DNA#A11#G00135
950
+ </Description>
951
+ <Data-Processing>
952
+ Illumina Genome Studio; the non_normalized.txt contains unmethylated (A) and methylated (B) signal intensities.
953
+ </Data-Processing>
954
+ <Platform-Ref ref="GPL13534" />
955
+ <Contact-Ref ref="contrib1" />
956
+ <Supplementary-Data type="unknown">
957
+ NONE
958
+ </Supplementary-Data>
959
+ <Data-Table>
960
+ <Column position="1">
961
+ <Name>ID_REF</Name>
962
+ </Column>
963
+ <Column position="2">
964
+ <Name>VALUE</Name>
965
+ <Description>Average Beta</Description>
966
+ </Column>
967
+ <Column position="3">
968
+ <Name>Detection Pval</Name>
969
+ </Column>
970
+ <External-Data rows="485577">
971
+ GSM1437769-tbl-1.txt
972
+ </External-Data>
973
+ </Data-Table>
974
+ </Sample>
975
+
976
+ <Sample iid="GSM1437770">
977
+ <Status database="GEO">
978
+ <Submission-Date>2014-07-16</Submission-Date>
979
+ <Release-Date>2014-08-12</Release-Date>
980
+ <Last-Update-Date>2014-08-12</Last-Update-Date>
981
+ </Status>
982
+ <Title>PBMC genomic DNA_Control6</Title>
983
+ <Accession database="GEO">GSM1437770</Accession>
984
+ <Type>genomic</Type>
985
+ <Channel-Count>1</Channel-Count>
986
+ <Channel position="1">
987
+ <Source>Control PBMC</Source>
988
+ <Organism taxid="9606">Homo sapiens</Organism>
989
+ <Characteristics tag="gender">
990
+ female
991
+ </Characteristics>
992
+ <Characteristics tag="subject id">
993
+ Control subject 6
994
+ </Characteristics>
995
+ <Characteristics tag="disease state">
996
+ Control
997
+ </Characteristics>
998
+ <Characteristics tag="cell type">
999
+ peripheral blood mononuclear cells (PBMC)
1000
+ </Characteristics>
1001
+ <Molecule>genomic DNA</Molecule>
1002
+ <Extract-Protocol>
1003
+ Omega EZNA Tissue DNA Kit; Qiagen MinElute Reaction Cleanup Kit; Genome Quebec sample processing protocols
1004
+ </Extract-Protocol>
1005
+ <Label>Cy3,Cy5</Label>
1006
+ <Label-Protocol>
1007
+ Standard Illumina Protocol
1008
+ </Label-Protocol>
1009
+ </Channel>
1010
+ <Hybridization-Protocol>
1011
+ Standard Illumina Protocol
1012
+ </Hybridization-Protocol>
1013
+ <Scan-Protocol>
1014
+ Standard Illumina Protocol
1015
+ </Scan-Protocol>
1016
+ <Description>
1017
+ PBMC genomic DNA from Control subject 6
1018
+ 7985#WG0153568-DNA#A12#G00213
1019
+ </Description>
1020
+ <Data-Processing>
1021
+ Illumina Genome Studio; the non_normalized.txt contains unmethylated (A) and methylated (B) signal intensities.
1022
+ </Data-Processing>
1023
+ <Platform-Ref ref="GPL13534" />
1024
+ <Contact-Ref ref="contrib1" />
1025
+ <Supplementary-Data type="unknown">
1026
+ NONE
1027
+ </Supplementary-Data>
1028
+ <Data-Table>
1029
+ <Column position="1">
1030
+ <Name>ID_REF</Name>
1031
+ </Column>
1032
+ <Column position="2">
1033
+ <Name>VALUE</Name>
1034
+ <Description>Average Beta</Description>
1035
+ </Column>
1036
+ <Column position="3">
1037
+ <Name>Detection Pval</Name>
1038
+ </Column>
1039
+ <External-Data rows="485577">
1040
+ GSM1437770-tbl-1.txt
1041
+ </External-Data>
1042
+ </Data-Table>
1043
+ </Sample>
1044
+
1045
+ <Sample iid="GSM1437771">
1046
+ <Status database="GEO">
1047
+ <Submission-Date>2014-07-16</Submission-Date>
1048
+ <Release-Date>2014-08-12</Release-Date>
1049
+ <Last-Update-Date>2014-08-12</Last-Update-Date>
1050
+ </Status>
1051
+ <Title>PBMC genomic DNA_CFS7</Title>
1052
+ <Accession database="GEO">GSM1437771</Accession>
1053
+ <Type>genomic</Type>
1054
+ <Channel-Count>1</Channel-Count>
1055
+ <Channel position="1">
1056
+ <Source>CFS PBMC</Source>
1057
+ <Organism taxid="9606">Homo sapiens</Organism>
1058
+ <Characteristics tag="gender">
1059
+ female
1060
+ </Characteristics>
1061
+ <Characteristics tag="subject id">
1062
+ CFS subject 7
1063
+ </Characteristics>
1064
+ <Characteristics tag="disease state">
1065
+ Chronic Fatigue Syndrome (CFS)
1066
+ </Characteristics>
1067
+ <Characteristics tag="cell type">
1068
+ peripheral blood mononuclear cells (PBMC)
1069
+ </Characteristics>
1070
+ <Molecule>genomic DNA</Molecule>
1071
+ <Extract-Protocol>
1072
+ Omega EZNA Tissue DNA Kit; Qiagen MinElute Reaction Cleanup Kit; Genome Quebec sample processing protocols
1073
+ </Extract-Protocol>
1074
+ <Label>Cy3,Cy5</Label>
1075
+ <Label-Protocol>
1076
+ Standard Illumina Protocol
1077
+ </Label-Protocol>
1078
+ </Channel>
1079
+ <Hybridization-Protocol>
1080
+ Standard Illumina Protocol
1081
+ </Hybridization-Protocol>
1082
+ <Scan-Protocol>
1083
+ Standard Illumina Protocol
1084
+ </Scan-Protocol>
1085
+ <Description>
1086
+ PBMC genomic DNA from CFS subject 7
1087
+ 7985#WG0153568-DNA#B01#G00021
1088
+ </Description>
1089
+ <Data-Processing>
1090
+ Illumina Genome Studio; the non_normalized.txt contains unmethylated (A) and methylated (B) signal intensities.
1091
+ </Data-Processing>
1092
+ <Platform-Ref ref="GPL13534" />
1093
+ <Contact-Ref ref="contrib1" />
1094
+ <Supplementary-Data type="unknown">
1095
+ NONE
1096
+ </Supplementary-Data>
1097
+ <Data-Table>
1098
+ <Column position="1">
1099
+ <Name>ID_REF</Name>
1100
+ </Column>
1101
+ <Column position="2">
1102
+ <Name>VALUE</Name>
1103
+ <Description>Average Beta</Description>
1104
+ </Column>
1105
+ <Column position="3">
1106
+ <Name>Detection Pval</Name>
1107
+ </Column>
1108
+ <External-Data rows="485577">
1109
+ GSM1437771-tbl-1.txt
1110
+ </External-Data>
1111
+ </Data-Table>
1112
+ </Sample>
1113
+
1114
+ <Sample iid="GSM1437772">
1115
+ <Status database="GEO">
1116
+ <Submission-Date>2014-07-16</Submission-Date>
1117
+ <Release-Date>2014-08-12</Release-Date>
1118
+ <Last-Update-Date>2014-08-12</Last-Update-Date>
1119
+ </Status>
1120
+ <Title>PBMC genomic DNA_CFS8</Title>
1121
+ <Accession database="GEO">GSM1437772</Accession>
1122
+ <Type>genomic</Type>
1123
+ <Channel-Count>1</Channel-Count>
1124
+ <Channel position="1">
1125
+ <Source>CFS PBMC</Source>
1126
+ <Organism taxid="9606">Homo sapiens</Organism>
1127
+ <Characteristics tag="gender">
1128
+ female
1129
+ </Characteristics>
1130
+ <Characteristics tag="subject id">
1131
+ CFS subject 8
1132
+ </Characteristics>
1133
+ <Characteristics tag="disease state">
1134
+ Chronic Fatigue Syndrome (CFS)
1135
+ </Characteristics>
1136
+ <Characteristics tag="cell type">
1137
+ peripheral blood mononuclear cells (PBMC)
1138
+ </Characteristics>
1139
+ <Molecule>genomic DNA</Molecule>
1140
+ <Extract-Protocol>
1141
+ Omega EZNA Tissue DNA Kit; Qiagen MinElute Reaction Cleanup Kit; Genome Quebec sample processing protocols
1142
+ </Extract-Protocol>
1143
+ <Label>Cy3,Cy5</Label>
1144
+ <Label-Protocol>
1145
+ Standard Illumina Protocol
1146
+ </Label-Protocol>
1147
+ </Channel>
1148
+ <Hybridization-Protocol>
1149
+ Standard Illumina Protocol
1150
+ </Hybridization-Protocol>
1151
+ <Scan-Protocol>
1152
+ Standard Illumina Protocol
1153
+ </Scan-Protocol>
1154
+ <Description>
1155
+ PBMC genomic DNA from CFS subject 8
1156
+ 7985#WG0153568-DNA#B02#G00059
1157
+ </Description>
1158
+ <Data-Processing>
1159
+ Illumina Genome Studio; the non_normalized.txt contains unmethylated (A) and methylated (B) signal intensities.
1160
+ </Data-Processing>
1161
+ <Platform-Ref ref="GPL13534" />
1162
+ <Contact-Ref ref="contrib1" />
1163
+ <Supplementary-Data type="unknown">
1164
+ NONE
1165
+ </Supplementary-Data>
1166
+ <Data-Table>
1167
+ <Column position="1">
1168
+ <Name>ID_REF</Name>
1169
+ </Column>
1170
+ <Column position="2">
1171
+ <Name>VALUE</Name>
1172
+ <Description>Average Beta</Description>
1173
+ </Column>
1174
+ <Column position="3">
1175
+ <Name>Detection Pval</Name>
1176
+ </Column>
1177
+ <External-Data rows="485577">
1178
+ GSM1437772-tbl-1.txt
1179
+ </External-Data>
1180
+ </Data-Table>
1181
+ </Sample>
1182
+
1183
+ <Sample iid="GSM1437773">
1184
+ <Status database="GEO">
1185
+ <Submission-Date>2014-07-16</Submission-Date>
1186
+ <Release-Date>2014-08-12</Release-Date>
1187
+ <Last-Update-Date>2014-08-12</Last-Update-Date>
1188
+ </Status>
1189
+ <Title>PBMC genomic DNA_CFS9</Title>
1190
+ <Accession database="GEO">GSM1437773</Accession>
1191
+ <Type>genomic</Type>
1192
+ <Channel-Count>1</Channel-Count>
1193
+ <Channel position="1">
1194
+ <Source>CFS PBMC</Source>
1195
+ <Organism taxid="9606">Homo sapiens</Organism>
1196
+ <Characteristics tag="gender">
1197
+ female
1198
+ </Characteristics>
1199
+ <Characteristics tag="subject id">
1200
+ CFS subject 9
1201
+ </Characteristics>
1202
+ <Characteristics tag="disease state">
1203
+ Chronic Fatigue Syndrome (CFS)
1204
+ </Characteristics>
1205
+ <Characteristics tag="cell type">
1206
+ peripheral blood mononuclear cells (PBMC)
1207
+ </Characteristics>
1208
+ <Molecule>genomic DNA</Molecule>
1209
+ <Extract-Protocol>
1210
+ Omega EZNA Tissue DNA Kit; Qiagen MinElute Reaction Cleanup Kit; Genome Quebec sample processing protocols
1211
+ </Extract-Protocol>
1212
+ <Label>Cy3,Cy5</Label>
1213
+ <Label-Protocol>
1214
+ Standard Illumina Protocol
1215
+ </Label-Protocol>
1216
+ </Channel>
1217
+ <Hybridization-Protocol>
1218
+ Standard Illumina Protocol
1219
+ </Hybridization-Protocol>
1220
+ <Scan-Protocol>
1221
+ Standard Illumina Protocol
1222
+ </Scan-Protocol>
1223
+ <Description>
1224
+ PBMC genomic DNA from CFS subject 9
1225
+ 7985#WG0153568-DNA#B03#G00054
1226
+ </Description>
1227
+ <Data-Processing>
1228
+ Illumina Genome Studio; the non_normalized.txt contains unmethylated (A) and methylated (B) signal intensities.
1229
+ </Data-Processing>
1230
+ <Platform-Ref ref="GPL13534" />
1231
+ <Contact-Ref ref="contrib1" />
1232
+ <Supplementary-Data type="unknown">
1233
+ NONE
1234
+ </Supplementary-Data>
1235
+ <Data-Table>
1236
+ <Column position="1">
1237
+ <Name>ID_REF</Name>
1238
+ </Column>
1239
+ <Column position="2">
1240
+ <Name>VALUE</Name>
1241
+ <Description>Average Beta</Description>
1242
+ </Column>
1243
+ <Column position="3">
1244
+ <Name>Detection Pval</Name>
1245
+ </Column>
1246
+ <External-Data rows="485577">
1247
+ GSM1437773-tbl-1.txt
1248
+ </External-Data>
1249
+ </Data-Table>
1250
+ </Sample>
1251
+
1252
+ <Sample iid="GSM1437774">
1253
+ <Status database="GEO">
1254
+ <Submission-Date>2014-07-16</Submission-Date>
1255
+ <Release-Date>2014-08-12</Release-Date>
1256
+ <Last-Update-Date>2014-08-12</Last-Update-Date>
1257
+ </Status>
1258
+ <Title>PBMC genomic DNA_CFS10</Title>
1259
+ <Accession database="GEO">GSM1437774</Accession>
1260
+ <Type>genomic</Type>
1261
+ <Channel-Count>1</Channel-Count>
1262
+ <Channel position="1">
1263
+ <Source>CFS PBMC</Source>
1264
+ <Organism taxid="9606">Homo sapiens</Organism>
1265
+ <Characteristics tag="gender">
1266
+ female
1267
+ </Characteristics>
1268
+ <Characteristics tag="subject id">
1269
+ CFS subject 10
1270
+ </Characteristics>
1271
+ <Characteristics tag="disease state">
1272
+ Chronic Fatigue Syndrome (CFS)
1273
+ </Characteristics>
1274
+ <Characteristics tag="cell type">
1275
+ peripheral blood mononuclear cells (PBMC)
1276
+ </Characteristics>
1277
+ <Molecule>genomic DNA</Molecule>
1278
+ <Extract-Protocol>
1279
+ Omega EZNA Tissue DNA Kit; Qiagen MinElute Reaction Cleanup Kit; Genome Quebec sample processing protocols
1280
+ </Extract-Protocol>
1281
+ <Label>Cy3,Cy5</Label>
1282
+ <Label-Protocol>
1283
+ Standard Illumina Protocol
1284
+ </Label-Protocol>
1285
+ </Channel>
1286
+ <Hybridization-Protocol>
1287
+ Standard Illumina Protocol
1288
+ </Hybridization-Protocol>
1289
+ <Scan-Protocol>
1290
+ Standard Illumina Protocol
1291
+ </Scan-Protocol>
1292
+ <Description>
1293
+ PBMC genomic DNA from CFS subject 10
1294
+ 7985#WG0153568-DNA#B04#G00030
1295
+ </Description>
1296
+ <Data-Processing>
1297
+ Illumina Genome Studio; the non_normalized.txt contains unmethylated (A) and methylated (B) signal intensities.
1298
+ </Data-Processing>
1299
+ <Platform-Ref ref="GPL13534" />
1300
+ <Contact-Ref ref="contrib1" />
1301
+ <Supplementary-Data type="unknown">
1302
+ NONE
1303
+ </Supplementary-Data>
1304
+ <Data-Table>
1305
+ <Column position="1">
1306
+ <Name>ID_REF</Name>
1307
+ </Column>
1308
+ <Column position="2">
1309
+ <Name>VALUE</Name>
1310
+ <Description>Average Beta</Description>
1311
+ </Column>
1312
+ <Column position="3">
1313
+ <Name>Detection Pval</Name>
1314
+ </Column>
1315
+ <External-Data rows="485577">
1316
+ GSM1437774-tbl-1.txt
1317
+ </External-Data>
1318
+ </Data-Table>
1319
+ </Sample>
1320
+
1321
+ <Sample iid="GSM1437775">
1322
+ <Status database="GEO">
1323
+ <Submission-Date>2014-07-16</Submission-Date>
1324
+ <Release-Date>2014-08-12</Release-Date>
1325
+ <Last-Update-Date>2014-08-12</Last-Update-Date>
1326
+ </Status>
1327
+ <Title>PBMC genomic DNA_CFS11</Title>
1328
+ <Accession database="GEO">GSM1437775</Accession>
1329
+ <Type>genomic</Type>
1330
+ <Channel-Count>1</Channel-Count>
1331
+ <Channel position="1">
1332
+ <Source>CFS PBMC</Source>
1333
+ <Organism taxid="9606">Homo sapiens</Organism>
1334
+ <Characteristics tag="gender">
1335
+ female
1336
+ </Characteristics>
1337
+ <Characteristics tag="subject id">
1338
+ CFS subject 11
1339
+ </Characteristics>
1340
+ <Characteristics tag="disease state">
1341
+ Chronic Fatigue Syndrome (CFS)
1342
+ </Characteristics>
1343
+ <Characteristics tag="cell type">
1344
+ peripheral blood mononuclear cells (PBMC)
1345
+ </Characteristics>
1346
+ <Molecule>genomic DNA</Molecule>
1347
+ <Extract-Protocol>
1348
+ Omega EZNA Tissue DNA Kit; Qiagen MinElute Reaction Cleanup Kit; Genome Quebec sample processing protocols
1349
+ </Extract-Protocol>
1350
+ <Label>Cy3,Cy5</Label>
1351
+ <Label-Protocol>
1352
+ Standard Illumina Protocol
1353
+ </Label-Protocol>
1354
+ </Channel>
1355
+ <Hybridization-Protocol>
1356
+ Standard Illumina Protocol
1357
+ </Hybridization-Protocol>
1358
+ <Scan-Protocol>
1359
+ Standard Illumina Protocol
1360
+ </Scan-Protocol>
1361
+ <Description>
1362
+ PBMC genomic DNA from CFS subject 11
1363
+ 7985#WG0153568-DNA#B05#G00121
1364
+ </Description>
1365
+ <Data-Processing>
1366
+ Illumina Genome Studio; the non_normalized.txt contains unmethylated (A) and methylated (B) signal intensities.
1367
+ </Data-Processing>
1368
+ <Platform-Ref ref="GPL13534" />
1369
+ <Contact-Ref ref="contrib1" />
1370
+ <Supplementary-Data type="unknown">
1371
+ NONE
1372
+ </Supplementary-Data>
1373
+ <Data-Table>
1374
+ <Column position="1">
1375
+ <Name>ID_REF</Name>
1376
+ </Column>
1377
+ <Column position="2">
1378
+ <Name>VALUE</Name>
1379
+ <Description>Average Beta</Description>
1380
+ </Column>
1381
+ <Column position="3">
1382
+ <Name>Detection Pval</Name>
1383
+ </Column>
1384
+ <External-Data rows="485577">
1385
+ GSM1437775-tbl-1.txt
1386
+ </External-Data>
1387
+ </Data-Table>
1388
+ </Sample>
1389
+
1390
+ <Sample iid="GSM1437776">
1391
+ <Status database="GEO">
1392
+ <Submission-Date>2014-07-16</Submission-Date>
1393
+ <Release-Date>2014-08-12</Release-Date>
1394
+ <Last-Update-Date>2014-08-12</Last-Update-Date>
1395
+ </Status>
1396
+ <Title>PBMC genomic DNA_CFS12</Title>
1397
+ <Accession database="GEO">GSM1437776</Accession>
1398
+ <Type>genomic</Type>
1399
+ <Channel-Count>1</Channel-Count>
1400
+ <Channel position="1">
1401
+ <Source>CFS PBMC</Source>
1402
+ <Organism taxid="9606">Homo sapiens</Organism>
1403
+ <Characteristics tag="gender">
1404
+ female
1405
+ </Characteristics>
1406
+ <Characteristics tag="subject id">
1407
+ CFS subject 12
1408
+ </Characteristics>
1409
+ <Characteristics tag="disease state">
1410
+ Chronic Fatigue Syndrome (CFS)
1411
+ </Characteristics>
1412
+ <Characteristics tag="cell type">
1413
+ peripheral blood mononuclear cells (PBMC)
1414
+ </Characteristics>
1415
+ <Molecule>genomic DNA</Molecule>
1416
+ <Extract-Protocol>
1417
+ Omega EZNA Tissue DNA Kit; Qiagen MinElute Reaction Cleanup Kit; Genome Quebec sample processing protocols
1418
+ </Extract-Protocol>
1419
+ <Label>Cy3,Cy5</Label>
1420
+ <Label-Protocol>
1421
+ Standard Illumina Protocol
1422
+ </Label-Protocol>
1423
+ </Channel>
1424
+ <Hybridization-Protocol>
1425
+ Standard Illumina Protocol
1426
+ </Hybridization-Protocol>
1427
+ <Scan-Protocol>
1428
+ Standard Illumina Protocol
1429
+ </Scan-Protocol>
1430
+ <Description>
1431
+ PBMC genomic DNA from CFS subject 12
1432
+ 7985#WG0153568-DNA#B06#G00113
1433
+ </Description>
1434
+ <Data-Processing>
1435
+ Illumina Genome Studio; the non_normalized.txt contains unmethylated (A) and methylated (B) signal intensities.
1436
+ </Data-Processing>
1437
+ <Platform-Ref ref="GPL13534" />
1438
+ <Contact-Ref ref="contrib1" />
1439
+ <Supplementary-Data type="unknown">
1440
+ NONE
1441
+ </Supplementary-Data>
1442
+ <Data-Table>
1443
+ <Column position="1">
1444
+ <Name>ID_REF</Name>
1445
+ </Column>
1446
+ <Column position="2">
1447
+ <Name>VALUE</Name>
1448
+ <Description>Average Beta</Description>
1449
+ </Column>
1450
+ <Column position="3">
1451
+ <Name>Detection Pval</Name>
1452
+ </Column>
1453
+ <External-Data rows="485577">
1454
+ GSM1437776-tbl-1.txt
1455
+ </External-Data>
1456
+ </Data-Table>
1457
+ </Sample>
1458
+
1459
+ <Sample iid="GSM1437777">
1460
+ <Status database="GEO">
1461
+ <Submission-Date>2014-07-16</Submission-Date>
1462
+ <Release-Date>2014-08-12</Release-Date>
1463
+ <Last-Update-Date>2014-08-12</Last-Update-Date>
1464
+ </Status>
1465
+ <Title>PBMC genomic DNA_Control7</Title>
1466
+ <Accession database="GEO">GSM1437777</Accession>
1467
+ <Type>genomic</Type>
1468
+ <Channel-Count>1</Channel-Count>
1469
+ <Channel position="1">
1470
+ <Source>Control PBMC</Source>
1471
+ <Organism taxid="9606">Homo sapiens</Organism>
1472
+ <Characteristics tag="gender">
1473
+ female
1474
+ </Characteristics>
1475
+ <Characteristics tag="subject id">
1476
+ Control subject 7
1477
+ </Characteristics>
1478
+ <Characteristics tag="disease state">
1479
+ Control
1480
+ </Characteristics>
1481
+ <Characteristics tag="cell type">
1482
+ peripheral blood mononuclear cells (PBMC)
1483
+ </Characteristics>
1484
+ <Molecule>genomic DNA</Molecule>
1485
+ <Extract-Protocol>
1486
+ Omega EZNA Tissue DNA Kit; Qiagen MinElute Reaction Cleanup Kit; Genome Quebec sample processing protocols
1487
+ </Extract-Protocol>
1488
+ <Label>Cy3,Cy5</Label>
1489
+ <Label-Protocol>
1490
+ Standard Illumina Protocol
1491
+ </Label-Protocol>
1492
+ </Channel>
1493
+ <Hybridization-Protocol>
1494
+ Standard Illumina Protocol
1495
+ </Hybridization-Protocol>
1496
+ <Scan-Protocol>
1497
+ Standard Illumina Protocol
1498
+ </Scan-Protocol>
1499
+ <Description>
1500
+ PBMC genomic DNA from Control subject 7
1501
+ 7985#WG0153568-DNA#B07#G00162
1502
+ </Description>
1503
+ <Data-Processing>
1504
+ Illumina Genome Studio; the non_normalized.txt contains unmethylated (A) and methylated (B) signal intensities.
1505
+ </Data-Processing>
1506
+ <Platform-Ref ref="GPL13534" />
1507
+ <Contact-Ref ref="contrib1" />
1508
+ <Supplementary-Data type="unknown">
1509
+ NONE
1510
+ </Supplementary-Data>
1511
+ <Data-Table>
1512
+ <Column position="1">
1513
+ <Name>ID_REF</Name>
1514
+ </Column>
1515
+ <Column position="2">
1516
+ <Name>VALUE</Name>
1517
+ <Description>Average Beta</Description>
1518
+ </Column>
1519
+ <Column position="3">
1520
+ <Name>Detection Pval</Name>
1521
+ </Column>
1522
+ <External-Data rows="485577">
1523
+ GSM1437777-tbl-1.txt
1524
+ </External-Data>
1525
+ </Data-Table>
1526
+ </Sample>
1527
+
1528
+ <Sample iid="GSM1437778">
1529
+ <Status database="GEO">
1530
+ <Submission-Date>2014-07-16</Submission-Date>
1531
+ <Release-Date>2014-08-12</Release-Date>
1532
+ <Last-Update-Date>2014-08-12</Last-Update-Date>
1533
+ </Status>
1534
+ <Title>PBMC genomic DNA_Control8</Title>
1535
+ <Accession database="GEO">GSM1437778</Accession>
1536
+ <Type>genomic</Type>
1537
+ <Channel-Count>1</Channel-Count>
1538
+ <Channel position="1">
1539
+ <Source>Control PBMC</Source>
1540
+ <Organism taxid="9606">Homo sapiens</Organism>
1541
+ <Characteristics tag="gender">
1542
+ female
1543
+ </Characteristics>
1544
+ <Characteristics tag="subject id">
1545
+ Control subject 8
1546
+ </Characteristics>
1547
+ <Characteristics tag="disease state">
1548
+ Control
1549
+ </Characteristics>
1550
+ <Characteristics tag="cell type">
1551
+ peripheral blood mononuclear cells (PBMC)
1552
+ </Characteristics>
1553
+ <Molecule>genomic DNA</Molecule>
1554
+ <Extract-Protocol>
1555
+ Omega EZNA Tissue DNA Kit; Qiagen MinElute Reaction Cleanup Kit; Genome Quebec sample processing protocols
1556
+ </Extract-Protocol>
1557
+ <Label>Cy3,Cy5</Label>
1558
+ <Label-Protocol>
1559
+ Standard Illumina Protocol
1560
+ </Label-Protocol>
1561
+ </Channel>
1562
+ <Hybridization-Protocol>
1563
+ Standard Illumina Protocol
1564
+ </Hybridization-Protocol>
1565
+ <Scan-Protocol>
1566
+ Standard Illumina Protocol
1567
+ </Scan-Protocol>
1568
+ <Description>
1569
+ PBMC genomic DNA from Control subject 8
1570
+ 7985#WG0153568-DNA#B08#G00208
1571
+ </Description>
1572
+ <Data-Processing>
1573
+ Illumina Genome Studio; the non_normalized.txt contains unmethylated (A) and methylated (B) signal intensities.
1574
+ </Data-Processing>
1575
+ <Platform-Ref ref="GPL13534" />
1576
+ <Contact-Ref ref="contrib1" />
1577
+ <Supplementary-Data type="unknown">
1578
+ NONE
1579
+ </Supplementary-Data>
1580
+ <Data-Table>
1581
+ <Column position="1">
1582
+ <Name>ID_REF</Name>
1583
+ </Column>
1584
+ <Column position="2">
1585
+ <Name>VALUE</Name>
1586
+ <Description>Average Beta</Description>
1587
+ </Column>
1588
+ <Column position="3">
1589
+ <Name>Detection Pval</Name>
1590
+ </Column>
1591
+ <External-Data rows="485577">
1592
+ GSM1437778-tbl-1.txt
1593
+ </External-Data>
1594
+ </Data-Table>
1595
+ </Sample>
1596
+
1597
+ <Sample iid="GSM1437779">
1598
+ <Status database="GEO">
1599
+ <Submission-Date>2014-07-16</Submission-Date>
1600
+ <Release-Date>2014-08-12</Release-Date>
1601
+ <Last-Update-Date>2014-08-12</Last-Update-Date>
1602
+ </Status>
1603
+ <Title>PBMC genomic DNA_Control9</Title>
1604
+ <Accession database="GEO">GSM1437779</Accession>
1605
+ <Type>genomic</Type>
1606
+ <Channel-Count>1</Channel-Count>
1607
+ <Channel position="1">
1608
+ <Source>Control PBMC</Source>
1609
+ <Organism taxid="9606">Homo sapiens</Organism>
1610
+ <Characteristics tag="gender">
1611
+ female
1612
+ </Characteristics>
1613
+ <Characteristics tag="subject id">
1614
+ Control subject 9
1615
+ </Characteristics>
1616
+ <Characteristics tag="disease state">
1617
+ Control
1618
+ </Characteristics>
1619
+ <Characteristics tag="cell type">
1620
+ peripheral blood mononuclear cells (PBMC)
1621
+ </Characteristics>
1622
+ <Molecule>genomic DNA</Molecule>
1623
+ <Extract-Protocol>
1624
+ Omega EZNA Tissue DNA Kit; Qiagen MinElute Reaction Cleanup Kit; Genome Quebec sample processing protocols
1625
+ </Extract-Protocol>
1626
+ <Label>Cy3,Cy5</Label>
1627
+ <Label-Protocol>
1628
+ Standard Illumina Protocol
1629
+ </Label-Protocol>
1630
+ </Channel>
1631
+ <Hybridization-Protocol>
1632
+ Standard Illumina Protocol
1633
+ </Hybridization-Protocol>
1634
+ <Scan-Protocol>
1635
+ Standard Illumina Protocol
1636
+ </Scan-Protocol>
1637
+ <Description>
1638
+ PBMC genomic DNA from Control subject 9
1639
+ 7985#WG0153568-DNA#B09#G00150
1640
+ </Description>
1641
+ <Data-Processing>
1642
+ Illumina Genome Studio; the non_normalized.txt contains unmethylated (A) and methylated (B) signal intensities.
1643
+ </Data-Processing>
1644
+ <Platform-Ref ref="GPL13534" />
1645
+ <Contact-Ref ref="contrib1" />
1646
+ <Supplementary-Data type="unknown">
1647
+ NONE
1648
+ </Supplementary-Data>
1649
+ <Data-Table>
1650
+ <Column position="1">
1651
+ <Name>ID_REF</Name>
1652
+ </Column>
1653
+ <Column position="2">
1654
+ <Name>VALUE</Name>
1655
+ <Description>Average Beta</Description>
1656
+ </Column>
1657
+ <Column position="3">
1658
+ <Name>Detection Pval</Name>
1659
+ </Column>
1660
+ <External-Data rows="485577">
1661
+ GSM1437779-tbl-1.txt
1662
+ </External-Data>
1663
+ </Data-Table>
1664
+ </Sample>
1665
+
1666
+ <Sample iid="GSM1437780">
1667
+ <Status database="GEO">
1668
+ <Submission-Date>2014-07-16</Submission-Date>
1669
+ <Release-Date>2014-08-12</Release-Date>
1670
+ <Last-Update-Date>2014-08-12</Last-Update-Date>
1671
+ </Status>
1672
+ <Title>PBMC genomic DNA_Control10</Title>
1673
+ <Accession database="GEO">GSM1437780</Accession>
1674
+ <Type>genomic</Type>
1675
+ <Channel-Count>1</Channel-Count>
1676
+ <Channel position="1">
1677
+ <Source>Control PBMC</Source>
1678
+ <Organism taxid="9606">Homo sapiens</Organism>
1679
+ <Characteristics tag="gender">
1680
+ female
1681
+ </Characteristics>
1682
+ <Characteristics tag="subject id">
1683
+ Control subject 10
1684
+ </Characteristics>
1685
+ <Characteristics tag="disease state">
1686
+ Control
1687
+ </Characteristics>
1688
+ <Characteristics tag="cell type">
1689
+ peripheral blood mononuclear cells (PBMC)
1690
+ </Characteristics>
1691
+ <Molecule>genomic DNA</Molecule>
1692
+ <Extract-Protocol>
1693
+ Omega EZNA Tissue DNA Kit; Qiagen MinElute Reaction Cleanup Kit; Genome Quebec sample processing protocols
1694
+ </Extract-Protocol>
1695
+ <Label>Cy3,Cy5</Label>
1696
+ <Label-Protocol>
1697
+ Standard Illumina Protocol
1698
+ </Label-Protocol>
1699
+ </Channel>
1700
+ <Hybridization-Protocol>
1701
+ Standard Illumina Protocol
1702
+ </Hybridization-Protocol>
1703
+ <Scan-Protocol>
1704
+ Standard Illumina Protocol
1705
+ </Scan-Protocol>
1706
+ <Description>
1707
+ PBMC genomic DNA from Control subject 10
1708
+ 7985#WG0153568-DNA#B10#G00199
1709
+ </Description>
1710
+ <Data-Processing>
1711
+ Illumina Genome Studio; the non_normalized.txt contains unmethylated (A) and methylated (B) signal intensities.
1712
+ </Data-Processing>
1713
+ <Platform-Ref ref="GPL13534" />
1714
+ <Contact-Ref ref="contrib1" />
1715
+ <Supplementary-Data type="unknown">
1716
+ NONE
1717
+ </Supplementary-Data>
1718
+ <Data-Table>
1719
+ <Column position="1">
1720
+ <Name>ID_REF</Name>
1721
+ </Column>
1722
+ <Column position="2">
1723
+ <Name>VALUE</Name>
1724
+ <Description>Average Beta</Description>
1725
+ </Column>
1726
+ <Column position="3">
1727
+ <Name>Detection Pval</Name>
1728
+ </Column>
1729
+ <External-Data rows="485577">
1730
+ GSM1437780-tbl-1.txt
1731
+ </External-Data>
1732
+ </Data-Table>
1733
+ </Sample>
1734
+
1735
+ <Sample iid="GSM1437781">
1736
+ <Status database="GEO">
1737
+ <Submission-Date>2014-07-16</Submission-Date>
1738
+ <Release-Date>2014-08-12</Release-Date>
1739
+ <Last-Update-Date>2014-08-12</Last-Update-Date>
1740
+ </Status>
1741
+ <Title>PBMC genomic DNA_Control11</Title>
1742
+ <Accession database="GEO">GSM1437781</Accession>
1743
+ <Type>genomic</Type>
1744
+ <Channel-Count>1</Channel-Count>
1745
+ <Channel position="1">
1746
+ <Source>Control PBMC</Source>
1747
+ <Organism taxid="9606">Homo sapiens</Organism>
1748
+ <Characteristics tag="gender">
1749
+ female
1750
+ </Characteristics>
1751
+ <Characteristics tag="subject id">
1752
+ Control subject 11
1753
+ </Characteristics>
1754
+ <Characteristics tag="disease state">
1755
+ Control
1756
+ </Characteristics>
1757
+ <Characteristics tag="cell type">
1758
+ peripheral blood mononuclear cells (PBMC)
1759
+ </Characteristics>
1760
+ <Molecule>genomic DNA</Molecule>
1761
+ <Extract-Protocol>
1762
+ Omega EZNA Tissue DNA Kit; Qiagen MinElute Reaction Cleanup Kit; Genome Quebec sample processing protocols
1763
+ </Extract-Protocol>
1764
+ <Label>Cy3,Cy5</Label>
1765
+ <Label-Protocol>
1766
+ Standard Illumina Protocol
1767
+ </Label-Protocol>
1768
+ </Channel>
1769
+ <Hybridization-Protocol>
1770
+ Standard Illumina Protocol
1771
+ </Hybridization-Protocol>
1772
+ <Scan-Protocol>
1773
+ Standard Illumina Protocol
1774
+ </Scan-Protocol>
1775
+ <Description>
1776
+ PBMC genomic DNA from Control subject 11
1777
+ 7985#WG0153568-DNA#B11#G00216
1778
+ </Description>
1779
+ <Data-Processing>
1780
+ Illumina Genome Studio; the non_normalized.txt contains unmethylated (A) and methylated (B) signal intensities.
1781
+ </Data-Processing>
1782
+ <Platform-Ref ref="GPL13534" />
1783
+ <Contact-Ref ref="contrib1" />
1784
+ <Supplementary-Data type="unknown">
1785
+ NONE
1786
+ </Supplementary-Data>
1787
+ <Data-Table>
1788
+ <Column position="1">
1789
+ <Name>ID_REF</Name>
1790
+ </Column>
1791
+ <Column position="2">
1792
+ <Name>VALUE</Name>
1793
+ <Description>Average Beta</Description>
1794
+ </Column>
1795
+ <Column position="3">
1796
+ <Name>Detection Pval</Name>
1797
+ </Column>
1798
+ <External-Data rows="485577">
1799
+ GSM1437781-tbl-1.txt
1800
+ </External-Data>
1801
+ </Data-Table>
1802
+ </Sample>
1803
+
1804
+ <Sample iid="GSM1437782">
1805
+ <Status database="GEO">
1806
+ <Submission-Date>2014-07-16</Submission-Date>
1807
+ <Release-Date>2014-08-12</Release-Date>
1808
+ <Last-Update-Date>2014-08-12</Last-Update-Date>
1809
+ </Status>
1810
+ <Title>PBMC genomic DNA_Control12</Title>
1811
+ <Accession database="GEO">GSM1437782</Accession>
1812
+ <Type>genomic</Type>
1813
+ <Channel-Count>1</Channel-Count>
1814
+ <Channel position="1">
1815
+ <Source>Control PBMC</Source>
1816
+ <Organism taxid="9606">Homo sapiens</Organism>
1817
+ <Characteristics tag="gender">
1818
+ female
1819
+ </Characteristics>
1820
+ <Characteristics tag="subject id">
1821
+ Control subject 12
1822
+ </Characteristics>
1823
+ <Characteristics tag="disease state">
1824
+ Control
1825
+ </Characteristics>
1826
+ <Characteristics tag="cell type">
1827
+ peripheral blood mononuclear cells (PBMC)
1828
+ </Characteristics>
1829
+ <Molecule>genomic DNA</Molecule>
1830
+ <Extract-Protocol>
1831
+ Omega EZNA Tissue DNA Kit; Qiagen MinElute Reaction Cleanup Kit; Genome Quebec sample processing protocols
1832
+ </Extract-Protocol>
1833
+ <Label>Cy3,Cy5</Label>
1834
+ <Label-Protocol>
1835
+ Standard Illumina Protocol
1836
+ </Label-Protocol>
1837
+ </Channel>
1838
+ <Hybridization-Protocol>
1839
+ Standard Illumina Protocol
1840
+ </Hybridization-Protocol>
1841
+ <Scan-Protocol>
1842
+ Standard Illumina Protocol
1843
+ </Scan-Protocol>
1844
+ <Description>
1845
+ PBMC genomic DNA from Control subject 12
1846
+ 7985#WG0153568-DNA#B12#G00143
1847
+ </Description>
1848
+ <Data-Processing>
1849
+ Illumina Genome Studio; the non_normalized.txt contains unmethylated (A) and methylated (B) signal intensities.
1850
+ </Data-Processing>
1851
+ <Platform-Ref ref="GPL13534" />
1852
+ <Contact-Ref ref="contrib1" />
1853
+ <Supplementary-Data type="unknown">
1854
+ NONE
1855
+ </Supplementary-Data>
1856
+ <Data-Table>
1857
+ <Column position="1">
1858
+ <Name>ID_REF</Name>
1859
+ </Column>
1860
+ <Column position="2">
1861
+ <Name>VALUE</Name>
1862
+ <Description>Average Beta</Description>
1863
+ </Column>
1864
+ <Column position="3">
1865
+ <Name>Detection Pval</Name>
1866
+ </Column>
1867
+ <External-Data rows="485577">
1868
+ GSM1437782-tbl-1.txt
1869
+ </External-Data>
1870
+ </Data-Table>
1871
+ </Sample>
1872
+
1873
+ <Series iid="GSE59489">
1874
+ <Status database="GEO">
1875
+ <Submission-Date>2014-07-16</Submission-Date>
1876
+ <Release-Date>2014-08-12</Release-Date>
1877
+ <Last-Update-Date>2019-03-22</Last-Update-Date>
1878
+ </Status>
1879
+ <Title>DNA methylation modifications associated with Chronic Fatigue Syndrome</Title>
1880
+ <Accession database="GEO">GSE59489</Accession>
1881
+ <Pubmed-ID>25111603</Pubmed-ID>
1882
+ <Summary>
1883
+ Chronic Fatigue Syndrome (CFS), also known as myalgic encephalomyelitis, is a complex multifactorial disease that is characterized by the persistent presence of fatigue and other particular symptoms for a minimum of 6 months. Symptoms fail to dissipate after sufficient rest and have major effects on the daily functioning of CFS sufferers. CFS is a multi-system disease with a heterogeneous patient population showing a wide variety of functional disabilities and its biological basis remains poorly understood. Stable alterations in gene function in the immune system have been reported in several studies of CFS. Epigenetic modifications have been implicated in long-term effects on gene function, however, to our knowledge, genome-wide epigenetic modifications associated with CFS have not been explored. We examined the DNA methylome in peripheral blood mononuclear cells isolated from CFS patients and healthy controls using the Illumina HumanMethylation450 BeadChip array, controlling for invariant probes and probes overlapping polymorphic sequences.
1884
+ </Summary>
1885
+ <Overall-Design>
1886
+ Genomic DNA from 24 peripheral blood mononuclear cells (PBMC) samples (12 CFS, 12 controls) were bisulfite-converted and hybridised to the Illumina Infinium HumanMethylation450 BeadChip. GenomeStudio files were generated and the data was analyzed using the Illumina Methylation Analyzer R package.
1887
+ </Overall-Design>
1888
+ <Type>Methylation profiling by genome tiling array</Type>
1889
+ <Contributor-Ref ref="contrib3" position="1" />
1890
+ <Contributor-Ref ref="contrib4" position="2" />
1891
+ <Contributor-Ref ref="contrib5" position="3" />
1892
+ <Contact-Ref ref="contrib1" />
1893
+ <Sample-Ref ref="GSM1437759" />
1894
+ <Sample-Ref ref="GSM1437760" />
1895
+ <Sample-Ref ref="GSM1437761" />
1896
+ <Sample-Ref ref="GSM1437762" />
1897
+ <Sample-Ref ref="GSM1437763" />
1898
+ <Sample-Ref ref="GSM1437764" />
1899
+ <Sample-Ref ref="GSM1437765" />
1900
+ <Sample-Ref ref="GSM1437766" />
1901
+ <Sample-Ref ref="GSM1437767" />
1902
+ <Sample-Ref ref="GSM1437768" />
1903
+ <Sample-Ref ref="GSM1437769" />
1904
+ <Sample-Ref ref="GSM1437770" />
1905
+ <Sample-Ref ref="GSM1437771" />
1906
+ <Sample-Ref ref="GSM1437772" />
1907
+ <Sample-Ref ref="GSM1437773" />
1908
+ <Sample-Ref ref="GSM1437774" />
1909
+ <Sample-Ref ref="GSM1437775" />
1910
+ <Sample-Ref ref="GSM1437776" />
1911
+ <Sample-Ref ref="GSM1437777" />
1912
+ <Sample-Ref ref="GSM1437778" />
1913
+ <Sample-Ref ref="GSM1437779" />
1914
+ <Sample-Ref ref="GSM1437780" />
1915
+ <Sample-Ref ref="GSM1437781" />
1916
+ <Sample-Ref ref="GSM1437782" />
1917
+ <Supplementary-Data type="TAR">
1918
+ ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE59nnn/GSE59489/suppl/GSE59489_RAW.tar
1919
+ </Supplementary-Data>
1920
+ <Supplementary-Data type="TXT">
1921
+ ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE59nnn/GSE59489/suppl/GSE59489_non_normalized.txt.gz
1922
+ </Supplementary-Data>
1923
+ <Relation type="BioProject" target="https://www.ncbi.nlm.nih.gov/bioproject/PRJNA255437" />
1924
+ </Series>
1925
+
1926
+ </MINiML>