<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>26(17)</volume><submitter>Weng MP</submitter><funding>Intramural NIH HHS</funding><pubmed_abstract>&lt;h4>Summary&lt;/h4>MamPhEA is a web application dedicated to understanding functional properties of mammalian gene sets based on mouse-mutant phenotypes. It allows users to conduct enrichment analysis on predefined or user-defined phenotypes, gives users the option to specify phenotypes derived from null mutations, produces easily comprehensible results and supports analyses on genes of all mammalian species with a fully sequenced genome.&lt;h4>Availability&lt;/h4>http://evol.nhri.org.tw/MamPhEA/.</pubmed_abstract><journal>Bioinformatics (Oxford, England)</journal><pagination>2212-3</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2922895</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>MamPhEA: a web tool for mammalian phenotype enrichment analysis.</pubmed_title><pmcid>PMC2922895</pmcid><pubmed_authors>Weng MP</pubmed_authors><pubmed_authors>Liao BY</pubmed_authors></additional><is_claimable>false</is_claimable><name>MamPhEA: a web tool for mammalian phenotype enrichment analysis.</name><description>&lt;h4>Summary&lt;/h4>MamPhEA is a web application dedicated to understanding functional properties of mammalian gene sets based on mouse-mutant phenotypes. It allows users to conduct enrichment analysis on predefined or user-defined phenotypes, gives users the option to specify phenotypes derived from null mutations, produces easily comprehensible results and supports analyses on genes of all mammalian species with a fully sequenced genome.&lt;h4>Availability&lt;/h4>http://evol.nhri.org.tw/MamPhEA/.</description><dates><release>2010-01-01T00:00:00Z</release><publication>2010 Sep</publication><modification>2024-11-08T22:10:43.767Z</modification><creation>2019-03-27T00:33:21Z</creation></dates><accession>S-EPMC2922895</accession><cross_references><pubmed>20605928</pubmed><doi>10.1093/bioinformatics/btq359</doi></cross_references></HashMap>