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      Massively parallel digital transcriptional profiling of single cells

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      1 , 1 , 1 , 1 , 1 , 1 , 1 , 1 , 1 , 1 , 2 , 1 , 1 , 1 , 3 , 1 , 1 , 1 , 1 , 1 , 1 , 1 , 1 , 4 , 4 , 5 , 4 , 6 , 2 , 7 , 8 , 2 , 4 , 4 , 1 , a , 1 , b , 2 , 6 , 8 , 9
      Nature Communications
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          Abstract

          Characterizing the transcriptome of individual cells is fundamental to understanding complex biological systems. We describe a droplet-based system that enables 3′ mRNA counting of tens of thousands of single cells per sample. Cell encapsulation, of up to 8 samples at a time, takes place in ∼6 min, with ∼50% cell capture efficiency. To demonstrate the system's technical performance, we collected transcriptome data from ∼250k single cells across 29 samples. We validated the sensitivity of the system and its ability to detect rare populations using cell lines and synthetic RNAs. We profiled 68k peripheral blood mononuclear cells to demonstrate the system's ability to characterize large immune populations. Finally, we used sequence variation in the transcriptome data to determine host and donor chimerism at single-cell resolution from bone marrow mononuclear cells isolated from transplant patients.

          Abstract

          Single-cell gene expression analysis is challenging. This work describes a new droplet-based single cell RNA-seq platform capable of processing tens of thousands of cells across 8 independent samples in minutes, and demonstrates cellular subtypes and host–donor chimerism in transplant patients.

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          Single-cell transcriptomics reveals bimodality in expression and splicing in immune cells

          Recent molecular studies have revealed that, even when derived from a seemingly homogenous population, individual cells can exhibit substantial differences in gene expression, protein levels, and phenotypic output 1–5 , with important functional consequences 4,5 . Existing studies of cellular heterogeneity, however, have typically measured only a few pre-selected RNAs 1,2 or proteins 5,6 simultaneously because genomic profiling methods 3 could not be applied to single cells until very recently 7–10 . Here, we use single-cell RNA-Seq to investigate heterogeneity in the response of bone marrow derived dendritic cells (BMDCs) to lipopolysaccharide (LPS). We find extensive, and previously unobserved, bimodal variation in mRNA abundance and splicing patterns, which we validate by RNA-fluorescence in situ hybridization (RNA-FISH) for select transcripts. In particular, hundreds of key immune genes are bimodally expressed across cells, surprisingly even for genes that are very highly expressed at the population average. Moreover, splicing patterns demonstrate previously unobserved levels of heterogeneity between cells. Some of the observed bimodality can be attributed to closely related, yet distinct, known maturity states of BMDCs; other portions reflect differences in the usage of key regulatory circuits. For example, we identify a module of 137 highly variable, yet co-regulated, antiviral response genes. Using cells from knockout mice, we show that variability in this module may be propagated through an interferon feedback circuit involving the transcriptional regulators Stat2 and Irf7. Our study demonstrates the power and promise of single-cell genomics in uncovering functional diversity between cells and in deciphering cell states and circuits.
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            Accounting for technical noise in single-cell RNA-seq experiments.

            Single-cell RNA-seq can yield valuable insights about the variability within a population of seemingly homogeneous cells. We developed a quantitative statistical method to distinguish true biological variability from the high levels of technical noise in single-cell experiments. Our approach quantifies the statistical significance of observed cell-to-cell variability in expression strength on a gene-by-gene basis. We validate our approach using two independent data sets from Arabidopsis thaliana and Mus musculus.
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              Dealing with label switching in mixture models

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                Author and article information

                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group
                2041-1723
                16 January 2017
                2017
                : 8
                : 14049
                Affiliations
                [1 ]10x Genomics Inc. , Pleasanton, California, 94566, USA
                [2 ]Translational Research Program, Public Health Sciences Division, Fred Hutchinson Cancer Research Center , Seattle, Washington 98109, USA
                [3 ]Department of Genome Sciences, University of Washington , Seattle, Washington 98195, USA
                [4 ]Clinical Research Division, Fred Hutchinson Cancer Research Center , Seattle, Washington 98109, USA
                [5 ]Seattle Cancer Care Alliance Clinical Immunogenetics Laboratory , Seattle, Washington 98109, USA
                [6 ]Department of Pathology, University of Washington , Seattle, Washington 98195, USA
                [7 ]Medical Scientist Training Program, University of Washington School of Medicine , Seattle, Washington 98195, USA
                [8 ]Molecular and Cellular Biology Graduate Program, University of Washington , Seattle, Washington 98195, USA
                [9 ]Human Biology Division, Fred Hutchinson Cancer Research Center , Seattle, Washington 98109, USA
                Author notes
                Author information
                http://orcid.org/0000-0003-0546-9652
                Article
                ncomms14049
                10.1038/ncomms14049
                5241818
                28091601
                dffa012c-4b24-4351-939c-382e3ab84e78
                Copyright © 2017, The Author(s)

                This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/

                History
                : 20 September 2016
                : 23 November 2016
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