<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Rosenbloom KR</submitter><funding>Howard Hughes Medical Institute</funding><funding>NHGRI NIH HHS</funding><pagination>D912-7</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3245183</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>40(Database issue)</volume><pubmed_abstract>The Encyclopedia of DNA Elements (ENCODE) Consortium is entering its 5th year of production-level effort generating high-quality whole-genome functional annotations of the human genome. The past year has brought the ENCODE compendium of functional elements to critical mass, with a diverse set of 27 biochemical assays now covering 200 distinct human cell types. Within the mouse genome, which has been under study by ENCODE groups for the past 2 years, 37 cell types have been assayed. Over 2000 individual experiments have been completed and submitted to the Data Coordination Center for public use. UCSC makes this data available on the quality-reviewed public Genome Browser (http://genome.ucsc.edu) and on an early-access Preview Browser (http://genome-preview.ucsc.edu). Visual browsing, data mining and download of raw and processed data files are all supported. An ENCODE portal (http://encodeproject.org) provides specialized tools and information about the ENCODE data sets.</pubmed_abstract><journal>Nucleic acids research</journal><pubmed_title>ENCODE whole-genome data in the UCSC Genome Browser: update 2012.</pubmed_title><pmcid>PMC3245183</pmcid><funding_grant_id>3P41HG002371-10S1</funding_grant_id><funding_grant_id>5U41HG004568-04</funding_grant_id><funding_grant_id>3U41HG004568-03S1</funding_grant_id><funding_grant_id>5P41HG002371-10</funding_grant_id><pubmed_authors>Wong MC</pubmed_authors><pubmed_authors>Dreszer TR</pubmed_authors><pubmed_authors>Learned K</pubmed_authors><pubmed_authors>Gravell RC</pubmed_authors><pubmed_authors>Raney BJ</pubmed_authors><pubmed_authors>Kuhn RM</pubmed_authors><pubmed_authors>Sloan CA</pubmed_authors><pubmed_authors>Harte RA</pubmed_authors><pubmed_authors>Diekhans M</pubmed_authors><pubmed_authors>Pohl A</pubmed_authors><pubmed_authors>Cline MS</pubmed_authors><pubmed_authors>Goldman M</pubmed_authors><pubmed_authors>Hinrichs AS</pubmed_authors><pubmed_authors>Kent WJ</pubmed_authors><pubmed_authors>Maddren M</pubmed_authors><pubmed_authors>Clawson H</pubmed_authors><pubmed_authors>Fujita PA</pubmed_authors><pubmed_authors>Rhead B</pubmed_authors><pubmed_authors>Rosenbloom KR</pubmed_authors><pubmed_authors>Haussler D</pubmed_authors><pubmed_authors>Kirkup VM</pubmed_authors><pubmed_authors>Karolchik D</pubmed_authors><pubmed_authors>Zweig AS</pubmed_authors><pubmed_authors>Meyer LR</pubmed_authors><pubmed_authors>Barber GP</pubmed_authors><pubmed_authors>Malladi VS</pubmed_authors><pubmed_authors>Long JC</pubmed_authors></additional><is_claimable>false</is_claimable><name>ENCODE whole-genome data in the UCSC Genome Browser: update 2012.</name><description>The Encyclopedia of DNA Elements (ENCODE) Consortium is entering its 5th year of production-level effort generating high-quality whole-genome functional annotations of the human genome. The past year has brought the ENCODE compendium of functional elements to critical mass, with a diverse set of 27 biochemical assays now covering 200 distinct human cell types. Within the mouse genome, which has been under study by ENCODE groups for the past 2 years, 37 cell types have been assayed. Over 2000 individual experiments have been completed and submitted to the Data Coordination Center for public use. UCSC makes this data available on the quality-reviewed public Genome Browser (http://genome.ucsc.edu) and on an early-access Preview Browser (http://genome-preview.ucsc.edu). Visual browsing, data mining and download of raw and processed data files are all supported. An ENCODE portal (http://encodeproject.org) provides specialized tools and information about the ENCODE data sets.</description><dates><release>2012-01-01T00:00:00Z</release><publication>2012 Jan</publication><modification>2024-10-18T00:48:16.536Z</modification><creation>2019-03-27T00:47:18Z</creation></dates><accession>S-EPMC3245183</accession><cross_references><pubmed>22075998</pubmed><doi>10.1093/nar/gkr1012</doi></cross_references></HashMap>