Highly Parallel Genome-wide Expression Profiling of Individual Cells Using Nanoliter Droplets

Evan Z. Macosko(Broad Institute), Anindita Basu(Broad Institute), Rahul Satija(Broad Institute), James Nemesh(Broad Institute), Karthik Shekhar(Broad Institute), Melissa Goldman(Broad Institute), Itay Tirosh(Broad Institute), Hon‐Cheong So(Boston Children's Hospital), Nolan Kamitaki(Broad Institute), Emily M. Martersteck(Harvard University), John J. Trombetta(Broad Institute), David A. Weitz(Harvard University), Joshua R. Sanes(Harvard University), Alex K. Shalek(Broad Institute), Aviv Regev(Broad Institute), Steven A. McCarroll(Broad Institute)
DSpace@MIT (Massachusetts Institute of Technology)
May 1, 2015
Cited by 0Open Access
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Abstract

Cells, the basic units of biological structure and function, vary broadly in type and state. Single-cell genomics can characterize cell identity and function, but limitations of ease and scale have prevented its broad application. Here we describe Drop-seq, a strategy for quickly profiling thousands of individual cells by separating them into nanoliter-sized aqueous droplets, associating a different barcode with each cells RNAs, and sequencing them all together. Drop-seq analyzes mRNA transcripts from thousands of individual cells simultaneously while remembering transcripts cell of origin. We analyzed transcriptomes from 44,808 mouse retinal cells and identified 39 transcriptionally distinct cell populations, creating a molecular atlas of gene expression for known retinal cell classes and novel candidate cell subtypes. Drop-seq will accelerate biological discovery by enabling routine transcriptional profiling at single-cell resolution. VIDEO ABSTRACT.


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