<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>31(3)</volume><submitter>Lim TY</submitter><funding>NIDDK NIH HHS</funding><journal>European journal of human genetics : EJHG</journal><pagination>275-277</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9995335</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>ParseCNV2: a versatile and integrated tool for copy number variation association studies.</pubmed_title><pmcid>PMC9995335</pmcid><funding_grant_id>R01 DK115574</funding_grant_id><funding_grant_id>P20 DK116191</funding_grant_id><funding_grant_id>R01 DK103184</funding_grant_id><pubmed_authors>Verbitsky M</pubmed_authors><pubmed_authors>Lim TY</pubmed_authors><pubmed_authors>Sanna-Cherchi S</pubmed_authors></additional><is_claimable>false</is_claimable><name>ParseCNV2: a versatile and integrated tool for copy number variation association studies.</name><description/><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Mar</publication><modification>2026-07-14T22:11:18.462Z</modification><creation>2025-04-06T11:03:40.822Z</creation></dates><accession>S-EPMC9995335</accession><cross_references><pubmed>36631543</pubmed><doi>10.1038/s41431-022-01280-x</doi></cross_references></HashMap>