Add longevitymap module (ported from Generation-I dna-seq/just_longevitymap)
Browse files- data/longevitymap/annotations.parquet +2 -2
- data/longevitymap/clin_sig_authority_calls.parquet +3 -0
- data/longevitymap/clin_sig_concordance.parquet +3 -0
- data/longevitymap/literature.parquet +2 -2
- data/longevitymap/manifest.json +242 -67
- data/longevitymap/sources.parquet +2 -2
- data/longevitymap/studies.parquet +2 -2
- data/longevitymap/weights.parquet +2 -2
data/longevitymap/annotations.parquet
CHANGED
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version https://git-lfs.github.com/spec/v1
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version https://git-lfs.github.com/spec/v1
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oid sha256:509aaa93046a23fbc9e9812d901bc98bfdd2144ed55635e946ebe35a034497fc
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size 22051
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data/longevitymap/clin_sig_authority_calls.parquet
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version https://git-lfs.github.com/spec/v1
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oid sha256:233b40fd79c7da73a9989ef4f7442886fd11d4495fbab9fe3a8d630855c9a1d4
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size 1138
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data/longevitymap/clin_sig_concordance.parquet
ADDED
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version https://git-lfs.github.com/spec/v1
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oid sha256:0611079ba1ae139bf1b1c3038d0f784a798747436c88275b47e6e986d10fe9a6
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size 919
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data/longevitymap/literature.parquet
CHANGED
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@@ -1,3 +1,3 @@
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version https://git-lfs.github.com/spec/v1
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oid sha256:
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size
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version https://git-lfs.github.com/spec/v1
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+
oid sha256:ae43c8821d72ca1ee34431fe13933bcbbba9fbdee85c7a8104f577cbdf2f7d94
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+
size 10565
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data/longevitymap/manifest.json
CHANGED
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@@ -2,10 +2,11 @@
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"manifest_version": "1.0",
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"schema_version": "1.0",
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"identity": {
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-
"namespace":
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"name": "longevitymap",
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-
"version":
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"
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},
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"display": {
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"title": "Longevity Map",
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@@ -19,14 +20,16 @@
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"curator": "just-dna-seq",
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"method": "expert-curated",
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"license": null,
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-
"
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"authors": [],
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"authorship": [],
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"created_at": null,
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-
"published_at":
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"stats": {
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"variant_count": 528,
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-
"weights_rows":
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"study_count": 671,
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"gene_count": 272,
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"genes": [
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},
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"compilation": {
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"compile_success": true,
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"compiled_by":
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"compiler_version": "just-dna-compiler 0.
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"ensembl_reference":
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"compiled_at": "2026-
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"warnings": [
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"
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"
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"rs479744: not found in resolution table, position remains unset",
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"rs4880: not found in resolution table, position remains unset",
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"rs4880: not found in resolution table, position remains unset",
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"rs660339: not found in resolution table, position remains unset",
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"rs660339: not found in resolution table, position remains unset",
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"rs660339: not found in resolution table, position remains unset",
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"rs660339: not found in resolution table, position remains unset",
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"rs28940577: not found in resolution table, position remains unset",
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"rs28940577: not found in resolution table, position remains unset",
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"rs1050450: not found in resolution table, position remains unset",
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"rs1050450: not found in resolution table, position remains unset",
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"rs13181: not found in resolution table, position remains unset",
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"rs11783247: not found in resolution table, position remains unset",
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"rs11783247: not found in resolution table, position remains unset",
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"rs3800358: not found in resolution table, position remains unset",
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"rs3800358: not found in resolution table, position remains unset",
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"rs1327533: not found in resolution table, position remains unset",
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"rs1327533: not found in resolution table, position remains unset",
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-
"literature.csv describes 36 citation(s) no study in this module cites: ['10583447', '11568114', '11602206', '11773214', '12152254', '12547486', '12954489', '14528043', '15569453', '16518704', '16611701', '16971231', '17182125', '18511746', '18761080', '19038839', '19249341', '20003469', '20304771', '20407924', '20800603', '21407828', '21782286', '21798861', '22008263', '22136229', '22456784', '22459618', '22912757', '22985084', '23128285', '23162014', '23186209', '24589862', '9170397', '9761238']",
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"sources.csv has no row for 1 source(s) the module's fact tables cite: ['pubmed'] — their terms are unrecorded."
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],
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"resolution_sources": [
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"cache"
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"ensembl"
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],
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"vrs_alleles":
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-
"vrs_alleles_identified":
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},
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"frequency": null,
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"gene_metrics": null,
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"literature": {
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-
"signature": "sha256:
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"sources": [
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"pubmed"
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],
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-
"row_count":
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-
"resolved_count":
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"missing_count": 0,
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-
"open_access_count":
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"abstract_only_count": 0,
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"quotes_authored": 0,
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-
"quotes_found": 0
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},
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"sources": {
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"signature": "sha256:b1c5043ccc97b5c15683fcdc1c63de32c6da8e270295619f2c4954817ed8332f",
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"sources": [
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@@ -405,59 +407,231 @@
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"redistribution": true,
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"row_count": 1
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},
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"inputs": [
|
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{
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"name": "module_spec.yaml",
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-
"sha256": "sha256:
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-
"size":
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},
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{
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"name": "variants.csv",
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-
"sha256": "sha256:
|
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-
"size":
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},
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{
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"name": "studies.csv",
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-
"sha256": "sha256:
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"size":
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}
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],
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"content_signature": "sha256:
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"artifact": {
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-
"digest": "sha256:
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"files": [
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{
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"name": "weights.parquet",
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-
"sha256": "sha256:
|
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-
"size":
|
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},
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{
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"name": "annotations.parquet",
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-
"sha256": "sha256:
|
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"size":
|
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},
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{
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"name": "studies.parquet",
|
| 441 |
-
"sha256": "sha256:
|
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-
"size":
|
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},
|
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{
|
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"name": "literature.parquet",
|
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"sha256": "sha256:
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"size":
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},
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{
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"name": "sources.parquet",
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-
"sha256": "sha256:
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"size":
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}
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]
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},
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"logs": [
|
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{
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"name": "v1_port.log",
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-
"sha256": "sha256:
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"size":
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}
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],
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"provenance": null,
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@@ -467,5 +641,6 @@
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| 467 |
"sha256": "sha256:ada3ef554ebc37eab2d5f63bf97a1ab68f49191cd13b2d4b1f69ab2ff399f570",
|
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"size": 85767
|
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"signature": null
|
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}
|
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|
| 2 |
"manifest_version": "1.0",
|
| 3 |
"schema_version": "1.0",
|
| 4 |
"identity": {
|
| 5 |
+
"namespace": "just-dna-seq",
|
| 6 |
"name": "longevitymap",
|
| 7 |
+
"version": "1.2.0",
|
| 8 |
+
"version_coerced_from": null,
|
| 9 |
+
"canonical_id": "just-dna-seq/longevitymap@1.2.0"
|
| 10 |
},
|
| 11 |
"display": {
|
| 12 |
"title": "Longevity Map",
|
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|
| 20 |
"curator": "just-dna-seq",
|
| 21 |
"method": "expert-curated",
|
| 22 |
"license": null,
|
| 23 |
+
"authority_precedence": [],
|
| 24 |
+
"weighting": null,
|
| 25 |
+
"owner": "just-dna-seq",
|
| 26 |
"authors": [],
|
| 27 |
"authorship": [],
|
| 28 |
"created_at": null,
|
| 29 |
+
"published_at": "2026-09-26T23:44:53Z",
|
| 30 |
"stats": {
|
| 31 |
"variant_count": 528,
|
| 32 |
+
"weights_rows": 1022,
|
| 33 |
"study_count": 671,
|
| 34 |
"gene_count": 272,
|
| 35 |
"genes": [
|
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| 326 |
},
|
| 327 |
"compilation": {
|
| 328 |
"compile_success": true,
|
| 329 |
+
"compiled_by": "marketplace-server",
|
| 330 |
+
"compiler_version": "just-dna-compiler 0.7.0",
|
| 331 |
+
"ensembl_reference": "just-dna-seq/ensembl_variations",
|
| 332 |
+
"compiled_at": "2026-09-26T23:44:53Z",
|
| 333 |
"warnings": [
|
| 334 |
+
"This module records no closure: nothing in it states that authoring is finished, so a consumer cannot tell a spec still being edited from one its author considers done. Run `just-dna-compiler close <spec-dir>` when the module is complete — closing is a deliberate act, it is never stamped by a passing check, and editing any authored file afterwards drops the closure again. Compiling without one is a warning today; requiring it is filed for 1.0 (RM73).",
|
| 335 |
+
"verification.json records 1 finding(s) across 1 check(s): citation_existence (1 of 126). A finding is a disagreement between this module and a source, not a defect — the archive is the stale side often enough that this never fails a build. Read the record's `detail` for which rows, and record why the module is right in `provenance.json`'s `outranks` where it is.",
|
| 336 |
+
"12 genotype(s) at 6 site(s) have no row: a heterozygous genotype has no row, so a carrier matches nothing in this module. The module states two or more genotypes at each of those sites, so this is a gap in a set the author started rather than a rule that fires once — e.g. rs2755209 A/C; rs2755209 A/T; rs2277509 A/C (+9 more)",
|
| 337 |
+
"192 genotype(s) at 186 site(s) have no row: a homozygous alternate genotype has no row, so a subject carrying two copies matches nothing in this module — the row that would describe them is the one missing. The module states two or more genotypes at each of those sites, so this is a gap in a set the author started rather than a rule that fires once — e.g. rs2802292 T/T; rs9536314 A/A; rs9536314 G/G (+189 more)",
|
| 338 |
+
"307 genotype(s) at 307 site(s) have no row: the reference homozygote has no row, so a subject carrying neither alternate matches nothing in this module. The module states two or more genotypes at each of those sites, so this is a gap in a set the author started rather than a rule that fires once — e.g. rs7412 C/C; rs429358 T/T; rs9536314 T/T (+304 more)"
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],
|
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+
"carried": [
|
| 341 |
+
"verification.json records 1 finding(s) across 1 check(s): citation_existence (1 of 126). A finding is a disagreement between this module and a source, not a defect — the archive is the stale side often enough that this never fails a build. Read the record's `detail` for which rows, and record why the module is right in `provenance.json`'s `outranks` where it is."
|
| 342 |
+
],
|
| 343 |
+
"warnings_summary": {
|
| 344 |
+
"genotype_coverage_gap": 3,
|
| 345 |
+
"module_not_closed": 1,
|
| 346 |
+
"verification_findings_recorded": 1
|
| 347 |
+
},
|
| 348 |
+
"dropped_rows": {},
|
| 349 |
+
"resolution_mode": "strict",
|
| 350 |
+
"fully_resolved": true,
|
| 351 |
+
"resolution_subjects": 1022,
|
| 352 |
+
"expanded_keys": 0,
|
| 353 |
+
"expanded_rows": 0,
|
| 354 |
+
"resolution_signature": "sha256:8d49dae7a51680776c2c3b0f6ec4e8edb1e5d6a3611e33e5c5accd2e1c9938b2",
|
| 355 |
"resolution_sources": [
|
| 356 |
+
"cache"
|
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|
| 357 |
],
|
| 358 |
+
"vrs_alleles": 900,
|
| 359 |
+
"vrs_alleles_identified": 900,
|
| 360 |
+
"positional_rows": 0,
|
| 361 |
+
"positional_rows_placed": 0
|
| 362 |
},
|
| 363 |
"frequency": null,
|
| 364 |
"gene_metrics": null,
|
| 365 |
+
"gene_validity": null,
|
| 366 |
+
"clinical_assertions": null,
|
| 367 |
+
"gwas_effects": null,
|
| 368 |
+
"expression_effects": null,
|
| 369 |
"literature": {
|
| 370 |
+
"signature": "sha256:8a18462371b9e8bb07255f5d7f48b7ae602fa325e1a784700411e685376c90d6",
|
| 371 |
"sources": [
|
| 372 |
"pubmed"
|
| 373 |
],
|
| 374 |
+
"row_count": 126,
|
| 375 |
+
"resolved_count": 126,
|
| 376 |
"missing_count": 0,
|
| 377 |
+
"open_access_count": 12,
|
| 378 |
"abstract_only_count": 0,
|
| 379 |
"quotes_authored": 0,
|
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