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dc.contributor.authorHie, Brian
dc.contributor.authorCho, Hyunghoon
dc.contributor.authorDeMeo, Benjamin
dc.contributor.authorBryson, Bryan
dc.contributor.authorBerger, Bonnie
dc.date.accessioned2021-10-27T20:23:04Z
dc.date.available2021-10-27T20:23:04Z
dc.date.issued2019
dc.identifier.urihttps://hdl.handle.net/1721.1/135349
dc.description.abstractLarge-scale single-cell RNA sequencing (scRNA-seq) studies that profile hundreds of thousands of cells are becoming increasingly common, overwhelming existing analysis pipelines. Here, we describe how to enhance and accelerate single-cell data analysis by summarizing the transcriptomic heterogeneity within a dataset using a small subset of cells, which we refer to as a geometric sketch. Our sketches provide more comprehensive visualization of transcriptional diversity, capture rare cell types with high sensitivity, and reveal biological cell types via clustering. Our sketch of umbilical cord blood cells uncovers a rare subpopulation of inflammatory macrophages, which we experimentally validated. The construction of our sketches is extremely fast, which enabled us to accelerate other crucial resource-intensive tasks, such as scRNA-seq data integration, while maintaining accuracy. We anticipate our algorithm will become an increasingly essential step when sharing and analyzing the rapidly growing volume of scRNA-seq data and help enable the democratization of single-cell omics.
dc.language.isoen
dc.publisherElsevier BV
dc.relation.isversionof10.1016/J.CELS.2019.05.003
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivs License
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourcePMC
dc.titleGeometric Sketching Compactly Summarizes the Single-Cell Transcriptomic Landscape
dc.typeArticle
dc.contributor.departmentMassachusetts Institute of Technology. Computer Science and Artificial Intelligence Laboratory
dc.contributor.departmentMassachusetts Institute of Technology. Department of Mathematics
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineering
dc.relation.journalCell Systems
dc.eprint.versionAuthor's final manuscript
dc.type.urihttp://purl.org/eprint/type/JournalArticle
eprint.statushttp://purl.org/eprint/status/PeerReviewed
dc.date.updated2020-07-20T14:37:56Z
dspace.orderedauthorsHie, B; Cho, H; DeMeo, B; Bryson, B; Berger, B
dspace.date.submission2020-07-20T14:38:04Z
mit.journal.volume8
mit.journal.issue6
mit.licensePUBLISHER_CC
mit.metadata.statusAuthority Work and Publication Information Needed


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