<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Tabula Sapiens Consortium*</submitter><funding>NIDDK NIH HHS</funding><funding>NHLBI NIH HHS</funding><funding>NIDCD NIH HHS</funding><pagination>eabl4896</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9812260</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>376(6594)</volume><pubmed_abstract>Molecular characterization of cell types using single-cell transcriptome sequencing is revolutionizing cell biology and enabling new insights into the physiology of human organs. We created a human reference atlas comprising nearly 500,000 cells from 24 different tissues and organs, many from the same donor. This atlas enabled molecular characterization of more than 400 cell types, their distribution across tissues, and tissue-specific variation in gene expression. Using multiple tissues from a single donor enabled identification of the clonal distribution of T cells between tissues, identification of the tissue-specific mutation rate in B cells, and analysis of the cell cycle state and proliferative potential of shared cell types across tissues. Cell type-specific RNA splicing was discove</pubmed_abstract><journal>Science (New York, N.Y.)</journal><pubmed_title>The Tabula Sapiens: A multiple-organ, single-cell transcriptomic atlas of humans.</pubmed_title><pmcid>PMC9812260</pmcid><funding_grant_id>P30 DK026743</funding_grant_id><funding_grant_id>R01 DK126482</funding_grant_id><funding_grant_id>R01 DC016892</funding_grant_id><funding_grant_id>R01 DK128932</funding_grant_id><funding_grant_id>T32 HL120824</funding_grant_id><pubmed_authors>Travaglini KJ</pubmed_authors><pubmed_authors>Houshdaran S</pubmed_authors><pubmed_authors>Loeb GB</pubmed_authors><pubmed_authors>Aaron KA</pubmed_authors><pubmed_authors>Kershner AM</pubmed_authors><pubmed_authors>Bean GR</pubmed_authors><pubmed_authors>Hemenez M</pubmed_authors><pubmed_authors>Wyss-Coray T</pubmed_authors><pubmed_authors>Vo KC</pubmed_authors><pubmed_authors>Chang CA</pubmed_authors><pubmed_authors>Xing G</pubmed_authors><pubmed_authors>Huang 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W</pubmed_authors><pubmed_authors>Irwin JC</pubmed_authors><pubmed_authors>Wu SM</pubmed_authors><pubmed_authors>Tabula Sapiens Consortium*</pubmed_authors><pubmed_authors>Rando TA</pubmed_authors><pubmed_authors>Harper W</pubmed_authors><pubmed_authors>Botvinnik OB</pubmed_authors><pubmed_authors>D'Amato G</pubmed_authors><pubmed_authors>Vanheusden R</pubmed_authors><pubmed_authors>Kelly B</pubmed_authors><pubmed_authors>Wu TTH</pubmed_authors><pubmed_authors>Jang S</pubmed_authors><pubmed_authors>Qi Z</pubmed_authors><pubmed_authors>Van Treuren W</pubmed_authors><pubmed_authors>Tarashansky AJ</pubmed_authors><pubmed_authors>Olivieri JE</pubmed_authors><pubmed_authors>Weinstein HNW</pubmed_authors><pubmed_authors>Clarke MF</pubmed_authors><pubmed_authors>Li B</pubmed_authors><pubmed_authors>Subramaniam VR</pubmed_authors><pubmed_authors>Phansalkar R</pubmed_authors><pubmed_authors>Culver RN</pubmed_authors><pubmed_authors>Mantri S</pubmed_authors><pubmed_authors>Crasta 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S</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Salzman J</pubmed_authors><pubmed_authors>Beyersdorf B</pubmed_authors><pubmed_authors>Kiss B</pubmed_authors><pubmed_authors>Sasagawa K</pubmed_authors><pubmed_authors>Hayashi A</pubmed_authors><pubmed_authors>Karkanias J</pubmed_authors><pubmed_authors>Puluca N</pubmed_authors><pubmed_authors>Bulthaup B</pubmed_authors></additional><is_claimable>false</is_claimable><name>The Tabula Sapiens: A multiple-organ, single-cell transcriptomic atlas of humans.</name><description>Molecular characterization of cell types using single-cell transcriptome sequencing is revolutionizing cell biology and enabling new insights into the physiology of human organs. We created a human reference atlas comprising nearly 500,000 cells from 24 different tissues and organs, many from the same donor. This atlas enabled molecular characterization of more than 400 cell types, their distribution across tissues, and tissue-specific variation in gene expression. Using multiple tissues from a single donor enabled identification of the clonal distribution of T cells between tissues, identification of the tissue-specific mutation rate in B cells, and analysis of the cell cycle state and proliferative potential of shared cell types across tissues. Cell type-specific RNA splicing was discove</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 May</publication><modification>2026-03-17T15:48:52.91Z</modification><creation>2025-04-07T05:06:31.339Z</creation></dates><accession>S-EPMC9812260</accession><cross_references><pubmed>35549404</pubmed><doi>10.1126/science.abl4896</doi></cross_references></HashMap>