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+  "accno" : "S-EPMC2913390",
+  "attributes" : [ {
+    "name" : "DataSource",
+    "value" : "Europe PMC"
+  }, {
+    "name" : "Title",
+    "value" : "Clustering phenotype populations by genome-wide RNAi and multiparametric imaging."
+  }, {
+    "name" : "ReleaseDate",
+    "value" : "2010-01-01"
+  }, {
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+    "value" : "EuropePMC"
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+  "section" : {
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+    "attributes" : [ {
+      "name" : "Title",
+      "value" : "Clustering phenotype populations by genome-wide RNAi and multiparametric imaging."
+    }, {
+      "name" : "Abstract",
+      "value" : "Genetic screens for phenotypic similarity have made key contributions to associating genes with biological processes. With RNA interference (RNAi), highly parallel phenotyping of loss-of-function effects in cells has become feasible. One of the current challenges however is the computational categorization of visual phenotypes and the prediction of biological function and processes. In this study, we describe a combined computational and experimental approach to discover novel gene functions and explore functional relationships. We performed a genome-wide RNAi screen in human cells and used quantitative descriptors derived from high-throughput imaging to generate multiparametric phenotypic profiles. We show that profiles predicted functions of genes by phenotypic similarity. Specifically, we examined several candidates including the largely uncharacterized gene DONSON, which shared phenotype similarity with known factors of DNA damage response (DDR) and genomic integrity. Experimental evidence supports that DONSON is a novel centrosomal protein required for DDR signalling and genomic integrity. Multiparametric phenotyping by automated imaging and computational annotation is a powerful method for functional discovery and mapping the landscape of phenotypic responses to cellular perturbations."
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+      "url" : "HPA023535",
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+      "type" : "Publication",
+      "attributes" : [ {
+        "name" : "Journal",
+        "value" : "Molecular systems biology"
+      }, {
+        "name" : "Volume",
+        "value" : "6"
+      }, {
+        "name" : "Pages",
+        "value" : "370"
+      }, {
+        "name" : "Publication date",
+        "value" : "2010 Jun"
+      } ],
+      "links" : [ [ {
+        "url" : "10.1038/msb.2010.25",
+        "attributes" : [ {
+          "name" : "Type",
+          "value" : "DOI"
+        } ]
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+        "url" : "PMC2913390",
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+          "value" : "PMC"
+        } ]
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+        "url" : "20531400",
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+          "name" : "Type",
+          "value" : "PMID"
+        } ]
+      } ] ]
+    }, {
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+        "name" : "Name",
+        "value" : "Fuchs F"
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+        "reference" : true
+      } ]
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+        "name" : "Name",
+        "value" : "Pau G"
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+        "value" : "Kranz D"
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+        "value" : "0000-0003-3604-7647"
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+        "name" : "Name",
+        "value" : "Sklyar O"
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+        "name" : "Name",
+        "value" : "Budjan C"
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+        "value" : "0000-0002-1563-9750"
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+      "attributes" : [ {
+        "name" : "Name",
+        "value" : "Steinbrink S"
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+        "value" : "Huber W"
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+      "type" : "Author",
+      "attributes" : [ {
+        "name" : "Name",
+        "value" : "Boutros M"
+      }, {
+        "name" : "ORCID",
+        "value" : "0000-0002-9458-817X"
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+      "type" : "Organization",
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+        "name" : "Name",
+        "value" : "EMBL, European Bioinformatics Institute, Wellcome Trust Genome Campus , Hinxton, Cambridge,"
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+        "value" : "EMBL, Genome Biology Unit , Heidelberg,"
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+        "value" : "German Cancer Research Center (DKFZ), Division of Signaling and Functional Genomics and Heidelberg University, Department of Cell and Molecular Biology, Medical Faculty Mannheim , Heidelberg,"
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+        "name" : "Name",
+        "value" : "German Cancer Research Center (DKFZ), Im Neuenheimer Feld 580, D-69120 Heidelberg, Germany"
+      } ]
+    } ]
+  },
+  "type" : "submission"
+}