A human cell atlas of fetal gene expression

Junyue Cao(University of Washington), Diana R. O’Day(University of Washington), Hannah A. Pliner(Brotman Baty Institute), Paul D. Kingsley(University of Rochester Medical Center), Mei Deng(University of Washington), Riza M. Daza(University of Washington), Michael Zager(Fred Hutch Cancer Center), Kimberly A. Aldinger(University of Washington), Ronnie Blecher‐Gonen(University of Washington), Fan Zhang(Illumina (United States)), Malte Spielmann(Max Planck Institute for Molecular Genetics), James Palis(University of Rochester Medical Center), Dan Doherty(University of Washington), Frank J. Steemers(Illumina (United States)), Ian A. Glass(University of Washington), Cole Trapnell(University of Washington), Jay Shendure(Howard Hughes Medical Institute)
Science
November 13, 2020
Cited by 825Open Access
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Abstract

The gene expression program underlying the specification of human cell types is of fundamental interest. We generated human cell atlases of gene expression and chromatin accessibility in fetal tissues. For gene expression, we applied three-level combinatorial indexing to >110 samples representing 15 organs, ultimately profiling ~4 million single cells. We leveraged the literature and other atlases to identify and annotate hundreds of cell types and subtypes, both within and across tissues. Our analyses focused on organ-specific specializations of broadly distributed cell types (such as blood, endothelial, and epithelial), sites of fetal erythropoiesis (which notably included the adrenal gland), and integration with mouse developmental atlases (such as conserved specification of blood cells). These data represent a rich resource for the exploration of in vivo human gene expression in diverse tissues and cell types.


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