<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Li D</submitter><funding>NHGRI NIH HHS</funding><funding>NIH</funding><funding>NIH HHS</funding><pagination>D1437-D1445</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12807646</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>54(D1)</volume><pubmed_abstract>Genomic variation between individuals is essential for understanding how differences in the genome sequence affect molecular and cellular processes. The Impact of Genomic Variation on Function (IGVF) Consortium aims to uncover the relationships among genomic variation, genome function, and phenotypes by combining experimental techniques, such as single-cell mapping and genomic perturbation assays, with computational approaches such as machine learning-based predictive modeling. The IGVF Data and Administrative Coordinating Centers collect, analyze, and disseminate data and results from across the consortium through an open-source platform called the IGVF Catalog. This resource includes, but is not limited to, data on the effects of coding variants on protein abundance and function, noncodi</pubmed_abstract><journal>Nucleic acids research</journal><pubmed_title>The IGVF catalog-from genetic variation to function.</pubmed_title><pmcid>PMC12807646</pmcid><funding_grant_id>UM1 HG012053</funding_grant_id><funding_grant_id>U24 HG012070</funding_grant_id><funding_grant_id>UM1HG011989</funding_grant_id><funding_grant_id>UM1 HG012010</funding_grant_id><funding_grant_id>U01 HG012009</funding_grant_id><funding_grant_id>UM1 HG011966</funding_grant_id><funding_grant_id>U01 HG012047</funding_grant_id><funding_grant_id>U01HG011967</funding_grant_id><funding_grant_id>UM1 HG011969</funding_grant_id><funding_grant_id>U01 HG011952</funding_grant_id><funding_grant_id>U01HG012059</funding_grant_id><funding_grant_id>UM1HG012003</funding_grant_id><funding_grant_id>U01 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M</pubmed_authors><pubmed_authors>Liu J</pubmed_authors><pubmed_authors>Bergquist T</pubmed_authors><pubmed_authors>Kagda M</pubmed_authors><pubmed_authors>Sverchkov Y</pubmed_authors><pubmed_authors>Zeiberg D</pubmed_authors><pubmed_authors>Liu S</pubmed_authors><pubmed_authors>Liu T</pubmed_authors><pubmed_authors>Dong S</pubmed_authors><pubmed_authors>Pejaver V</pubmed_authors><pubmed_authors>Whaling I</pubmed_authors><pubmed_authors>Hitz BC</pubmed_authors><pubmed_authors>Yue F</pubmed_authors><pubmed_authors>Wang T</pubmed_authors><pubmed_authors>Dey KK</pubmed_authors><pubmed_authors>Reddy TE</pubmed_authors><pubmed_authors>Chen Y</pubmed_authors><pubmed_authors>Love MI</pubmed_authors><pubmed_authors>Starita LM</pubmed_authors><pubmed_authors>Engreitz JM</pubmed_authors><pubmed_authors>Macias-Velasco JF</pubmed_authors><pubmed_authors>Montgomery MT</pubmed_authors><pubmed_authors>Jain S</pubmed_authors><pubmed_authors>Calderwood MA</pubmed_authors><pubmed_authors>Castro CP</pubmed_authors><pubmed_authors>Li D</pubmed_authors><pubmed_authors>Assis PR</pubmed_authors><pubmed_authors>Gersbach CA</pubmed_authors><pubmed_authors>Rozowsky J</pubmed_authors><pubmed_authors>Antonacci-Fulton L</pubmed_authors><pubmed_authors>Li M</pubmed_authors><pubmed_authors>Jolanki O</pubmed_authors><pubmed_authors>Zhang W</pubmed_authors><pubmed_authors>Boyle AP</pubmed_authors><pubmed_authors>Nzima MZ</pubmed_authors><pubmed_authors>Fowler DM</pubmed_authors><pubmed_authors>Craven M</pubmed_authors><pubmed_authors>Sinha R</pubmed_authors><pubmed_authors>Cody S</pubmed_authors><pubmed_authors>Huang Y</pubmed_authors><pubmed_authors>Cherry JM</pubmed_authors><pubmed_authors>Radivojac P</pubmed_authors><pubmed_authors>Sherpa RN</pubmed_authors><pubmed_authors>Majoros WH</pubmed_authors><pubmed_authors>Ma J</pubmed_authors><pubmed_authors>Ahituv N</pubmed_authors><pubmed_authors>Cai X</pubmed_authors></additional><is_claimable>false</is_claimable><name>The IGVF catalog-from genetic variation to function.</name><description>Genomic variation between individuals is essential for understanding how differences in the genome sequence affect molecular and cellular processes. The Impact of Genomic Variation on Function (IGVF) Consortium aims to uncover the relationships among genomic variation, genome function, and phenotypes by combining experimental techniques, such as single-cell mapping and genomic perturbation assays, with computational approaches such as machine learning-based predictive modeling. The IGVF Data and Administrative Coordinating Centers collect, analyze, and disseminate data and results from across the consortium through an open-source platform called the IGVF Catalog. This resource includes, but is not limited to, data on the effects of coding variants on protein abundance and function, noncodi</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Jan</publication><modification>2026-05-31T03:15:22.137Z</modification><creation>2026-05-31T03:10:11.574Z</creation></dates><accession>S-EPMC12807646</accession><cross_references><pubmed>41359121</pubmed><doi>10.1093/nar/gkaf1341</doi></cross_references></HashMap>