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SINCERA: A Pipeline for Single-Cell RNA-Seq Profiling Analysis
A major challenge in developmental biology is to understand the genetic and cellular processes/programs driving organ formation and differentiation of the diverse cell types that comprise the embryo. While recent studies using single cell transcriptome analysis illustrate the power to measure and un...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4658017/ https://www.ncbi.nlm.nih.gov/pubmed/26600239 http://dx.doi.org/10.1371/journal.pcbi.1004575 |
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author | Guo, Minzhe Wang, Hui Potter, S. Steven Whitsett, Jeffrey A. Xu, Yan |
author_facet | Guo, Minzhe Wang, Hui Potter, S. Steven Whitsett, Jeffrey A. Xu, Yan |
author_sort | Guo, Minzhe |
collection | PubMed |
description | A major challenge in developmental biology is to understand the genetic and cellular processes/programs driving organ formation and differentiation of the diverse cell types that comprise the embryo. While recent studies using single cell transcriptome analysis illustrate the power to measure and understand cellular heterogeneity in complex biological systems, processing large amounts of RNA-seq data from heterogeneous cell populations creates the need for readily accessible tools for the analysis of single-cell RNA-seq (scRNA-seq) profiles. The present study presents a generally applicable analytic pipeline (SINCERA: a computational pipeline for SINgle CEll RNA-seq profiling Analysis) for processing scRNA-seq data from a whole organ or sorted cells. The pipeline supports the analysis for: 1) the distinction and identification of major cell types; 2) the identification of cell type specific gene signatures; and 3) the determination of driving forces of given cell types. We applied this pipeline to the RNA-seq analysis of single cells isolated from embryonic mouse lung at E16.5. Through the pipeline analysis, we distinguished major cell types of fetal mouse lung, including epithelial, endothelial, smooth muscle, pericyte, and fibroblast-like cell types, and identified cell type specific gene signatures, bioprocesses, and key regulators. SINCERA is implemented in R, licensed under the GNU General Public License v3, and freely available from CCHMC PBGE website, https://research.cchmc.org/pbge/sincera.html. |
format | Online Article Text |
id | pubmed-4658017 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-46580172015-12-02 SINCERA: A Pipeline for Single-Cell RNA-Seq Profiling Analysis Guo, Minzhe Wang, Hui Potter, S. Steven Whitsett, Jeffrey A. Xu, Yan PLoS Comput Biol Research Article A major challenge in developmental biology is to understand the genetic and cellular processes/programs driving organ formation and differentiation of the diverse cell types that comprise the embryo. While recent studies using single cell transcriptome analysis illustrate the power to measure and understand cellular heterogeneity in complex biological systems, processing large amounts of RNA-seq data from heterogeneous cell populations creates the need for readily accessible tools for the analysis of single-cell RNA-seq (scRNA-seq) profiles. The present study presents a generally applicable analytic pipeline (SINCERA: a computational pipeline for SINgle CEll RNA-seq profiling Analysis) for processing scRNA-seq data from a whole organ or sorted cells. The pipeline supports the analysis for: 1) the distinction and identification of major cell types; 2) the identification of cell type specific gene signatures; and 3) the determination of driving forces of given cell types. We applied this pipeline to the RNA-seq analysis of single cells isolated from embryonic mouse lung at E16.5. Through the pipeline analysis, we distinguished major cell types of fetal mouse lung, including epithelial, endothelial, smooth muscle, pericyte, and fibroblast-like cell types, and identified cell type specific gene signatures, bioprocesses, and key regulators. SINCERA is implemented in R, licensed under the GNU General Public License v3, and freely available from CCHMC PBGE website, https://research.cchmc.org/pbge/sincera.html. Public Library of Science 2015-11-24 /pmc/articles/PMC4658017/ /pubmed/26600239 http://dx.doi.org/10.1371/journal.pcbi.1004575 Text en © 2015 Guo et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Guo, Minzhe Wang, Hui Potter, S. Steven Whitsett, Jeffrey A. Xu, Yan SINCERA: A Pipeline for Single-Cell RNA-Seq Profiling Analysis |
title | SINCERA: A Pipeline for Single-Cell RNA-Seq Profiling Analysis |
title_full | SINCERA: A Pipeline for Single-Cell RNA-Seq Profiling Analysis |
title_fullStr | SINCERA: A Pipeline for Single-Cell RNA-Seq Profiling Analysis |
title_full_unstemmed | SINCERA: A Pipeline for Single-Cell RNA-Seq Profiling Analysis |
title_short | SINCERA: A Pipeline for Single-Cell RNA-Seq Profiling Analysis |
title_sort | sincera: a pipeline for single-cell rna-seq profiling analysis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4658017/ https://www.ncbi.nlm.nih.gov/pubmed/26600239 http://dx.doi.org/10.1371/journal.pcbi.1004575 |
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