<HashMap><database>biostudies-literature</database><scores/><additional><submitter>All of Us Research Program Genomics Investigators</submitter><funding>NICHD NIH HHS</funding><funding>NHGRI NIH HHS</funding><funding>NIH HHS</funding><pagination>340-346</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10937371</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>627(8003)</volume><pubmed_abstract>Comprehensively mapping the genetic basis of human disease across diverse individuals is a long-standing goal for the field of human genetics&lt;sup>1-4&lt;/sup>. The All of Us Research Program is a longitudinal cohort study aiming to enrol a diverse group of at least one million individuals across the USA to accelerate biomedical research and improve human health&lt;sup>5,6&lt;/sup>. Here we describe the programme's genomics data release of 245,388 clinical-grade genome sequences. This resource is unique in its diversity as 77% of participants are from communities that are historically under-represented in biomedical research and 46% are individuals from under-represented racial and ethnic minorities. All of Us identified more than 1 billion genetic variants, including more than 275 million previousl</pubmed_abstract><journal>Nature</journal><pubmed_title>Genomic data in the All of Us Research Program.</pubmed_title><pmcid>PMC10937371</pmcid><funding_grant_id>OT2 OD002751</funding_grant_id><funding_grant_id>RM1 HG012334</funding_grant_id><funding_grant_id>OT2 OD002750</funding_grant_id><funding_grant_id>OT2 OD026548</funding_grant_id><funding_grant_id>OT2 OD025337</funding_grant_id><funding_grant_id>OT2 OD025315</funding_grant_id><funding_grant_id>OT2 OD026549</funding_grant_id><funding_grant_id>OT2 OD025277</funding_grant_id><funding_grant_id>OT2 OD025276</funding_grant_id><funding_grant_id>U24 OD023121</funding_grant_id><funding_grant_id>U24 OD023163</funding_grant_id><funding_grant_id>U2C OD023196</funding_grant_id><funding_grant_id>OT2 OD026555</funding_grant_id><funding_grant_id>OT2 OD026554</funding_grant_id><funding_grant_id>OT2 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SD</pubmed_authors><pubmed_authors>Blegen AL</pubmed_authors><pubmed_authors>Griffith SML</pubmed_authors><pubmed_authors>Wirkus SJ</pubmed_authors><pubmed_authors>Haessly A</pubmed_authors><pubmed_authors>Hatcher A</pubmed_authors><pubmed_authors>Ling H</pubmed_authors><pubmed_authors>Rura S</pubmed_authors><pubmed_authors>Lockwood CM</pubmed_authors><pubmed_authors>Mawhinney MZ</pubmed_authors><pubmed_authors>Gatzen M</pubmed_authors><pubmed_authors>Doheny KF</pubmed_authors><pubmed_authors>Walker K</pubmed_authors><pubmed_authors>Kachulis C</pubmed_authors><pubmed_authors>Aster MMT</pubmed_authors><pubmed_authors>Meller R</pubmed_authors><pubmed_authors>Lebo MS</pubmed_authors><pubmed_authors>Davis CP</pubmed_authors><pubmed_authors>Kovar CL</pubmed_authors><pubmed_authors>Hu J</pubmed_authors><pubmed_authors>Gauthier LD</pubmed_authors><pubmed_authors>Ramirez AH</pubmed_authors><pubmed_authors>Lennon NJ</pubmed_authors><pubmed_authors>Degatano 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D</pubmed_authors><pubmed_authors>Steeves M</pubmed_authors><pubmed_authors>Condon HR</pubmed_authors><pubmed_authors>Rehm HL</pubmed_authors><pubmed_authors>Larsson K</pubmed_authors><pubmed_authors>Boerwinkle E</pubmed_authors><pubmed_authors>Venner E</pubmed_authors><pubmed_authors>Glazer D</pubmed_authors><pubmed_authors>Green AE</pubmed_authors><pubmed_authors>Gabriel S</pubmed_authors><pubmed_authors>Ehmen BW</pubmed_authors><pubmed_authors>Able A</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Gupta N</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Zhou AY</pubmed_authors><pubmed_authors>Meyer JG</pubmed_authors><pubmed_authors>Sharma S</pubmed_authors><pubmed_authors>Ozenberger B</pubmed_authors><pubmed_authors>Metcalf GA</pubmed_authors><pubmed_authors>Radhakrishnan A</pubmed_authors><pubmed_authors>Cibulskis K</pubmed_authors><pubmed_authors>Pritchard CC</pubmed_authors><pubmed_authors>Harris PA</pubmed_authors><pubmed_authors>Richardson MA</pubmed_authors><pubmed_authors>Thibodeau SN</pubmed_authors><pubmed_authors>Patterson KE</pubmed_authors><pubmed_authors>Grant GB</pubmed_authors><pubmed_authors>Lim S</pubmed_authors><pubmed_authors>Khan Z</pubmed_authors><pubmed_authors>Lunt C</pubmed_authors><pubmed_authors>Harrison SM</pubmed_authors><pubmed_authors>Asch R</pubmed_authors><pubmed_authors>Shirts BH</pubmed_authors><pubmed_authors>Topper S</pubmed_authors><pubmed_authors>Neben CL</pubmed_authors><pubmed_authors>Mayo KR</pubmed_authors><pubmed_authors>Albach CH</pubmed_authors><pubmed_authors>Rosenthal EA</pubmed_authors><pubmed_authors>Banks E</pubmed_authors><pubmed_authors>Basford M</pubmed_authors><pubmed_authors>Austin-Tse C</pubmed_authors><pubmed_authors>Jordan IK</pubmed_authors><pubmed_authors>Schwartz S</pubmed_authors><pubmed_authors>Doddapaneni H</pubmed_authors><pubmed_authors>Lichtenstein L</pubmed_authors><pubmed_authors>Wagner VA</pubmed_authors><pubmed_authors>McGee S</pubmed_authors><pubmed_authors>Muzny DM</pubmed_authors><pubmed_authors>Wheeler MM</pubmed_authors><pubmed_authors>Wise AL</pubmed_authors><pubmed_authors>Baalawi W</pubmed_authors><pubmed_authors>Cicek MS</pubmed_authors><pubmed_authors>Choi SH</pubmed_authors><pubmed_authors>Eichler EE</pubmed_authors><pubmed_authors>Dillon MK</pubmed_authors><pubmed_authors>Bick AG</pubmed_authors></additional><is_claimable>false</is_claimable><name>Genomic data in the All of Us Research Program.</name><description>Comprehensively mapping the genetic basis of human disease across diverse individuals is a long-standing goal for the field of human genetics&lt;sup>1-4&lt;/sup>. The All of Us Research Program is a longitudinal cohort study aiming to enrol a diverse group of at least one million individuals across the USA to accelerate biomedical research and improve human health&lt;sup>5,6&lt;/sup>. Here we describe the programme's genomics data release of 245,388 clinical-grade genome sequences. This resource is unique in its diversity as 77% of participants are from communities that are historically under-represented in biomedical research and 46% are individuals from under-represented racial and ethnic minorities. All of Us identified more than 1 billion genetic variants, including more than 275 million previousl</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2026-06-02T22:53:41.59Z</modification><creation>2024-10-17T16:50:30.472Z</creation></dates><accession>S-EPMC10937371</accession><cross_references><pubmed>38374255</pubmed><doi>10.1038/s41586-023-06957-x</doi></cross_references></HashMap>