Bayesian approach to single-cell differential expression analysis

A method to model expression variability in single-cell RNA-seq measurements and thus to improve subsequent data analysis. Single-cell data provide a means to dissect the composition of complex tissues and specialized cellular environments. However, the analysis of such measurements is complicated b...

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Published inNature methods Vol. 11; no. 7; pp. 740 - 742
Main Authors Kharchenko, Peter V, Silberstein, Lev, Scadden, David T
Format Journal Article
LanguageEnglish
Published New York Nature Publishing Group US 01.07.2014
Nature Publishing Group
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Online AccessGet full text
ISSN1548-7091
1548-7105
1548-7105
DOI10.1038/nmeth.2967

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Abstract A method to model expression variability in single-cell RNA-seq measurements and thus to improve subsequent data analysis. Single-cell data provide a means to dissect the composition of complex tissues and specialized cellular environments. However, the analysis of such measurements is complicated by high levels of technical noise and intrinsic biological variability. We describe a probabilistic model of expression-magnitude distortions typical of single-cell RNA-sequencing measurements, which enables detection of differential expression signatures and identification of subpopulations of cells in a way that is more tolerant of noise.
AbstractList Single-cell data provide a means to dissect the composition of complex tissues and specialized cellular environments. However, the analysis of such measurements is complicated by high levels of technical noise and intrinsic biological variability. We describe a probabilistic model of expression-magnitude distortions typical of single-cell RNA-sequencing measurements, which enables detection of differential expression signatures and identification of subpopulations of cells in a way that is more tolerant of noise.
Single-cell data provide a means to dissect the composition of complex tissues and specialized cellular environments. However, the analysis of such measurements is complicated by high levels of technical noise and intrinsic biological variability. We describe a probabilistic model of expression-magnitude distortions typical of single-cell RNA-sequencing measurements, which enables detection of differential expression signatures and identification of subpopulations of cells in a way that is more tolerant of noise.Single-cell data provide a means to dissect the composition of complex tissues and specialized cellular environments. However, the analysis of such measurements is complicated by high levels of technical noise and intrinsic biological variability. We describe a probabilistic model of expression-magnitude distortions typical of single-cell RNA-sequencing measurements, which enables detection of differential expression signatures and identification of subpopulations of cells in a way that is more tolerant of noise.
A method to model expression variability in single-cell RNA-seq measurements and thus to improve subsequent data analysis. Single-cell data provide a means to dissect the composition of complex tissues and specialized cellular environments. However, the analysis of such measurements is complicated by high levels of technical noise and intrinsic biological variability. We describe a probabilistic model of expression-magnitude distortions typical of single-cell RNA-sequencing measurements, which enables detection of differential expression signatures and identification of subpopulations of cells in a way that is more tolerant of noise.
Single-cell data provides means to dissect the composition of complex tissues and specialized cellular environments. However, the analysis of such measurements is complicated by high levels of technical noise and intrinsic biological variability. We describe a probabilistic model of expression magnitude distortions typical of single-cell RNA sequencing measurements, which enables detection of differential expression signatures and identification of subpopulations of cells in a way that is more tolerant of noise.
Audience Academic
Author Kharchenko, Peter V
Scadden, David T
Silberstein, Lev
AuthorAffiliation 5 Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA, USA
2 Hematology/Oncology Program, Children's Hospital, Boston, MA, USA
3 Harvard Stem Cell Institute, Cambridge, MA, USA
1 Center for Biomedical Informatics, Harvard Medical School, Boston, MA, USA
4 Center for Regenerative Medicine, Massachusetts General Hospital, Boston, MA, USA
AuthorAffiliation_xml – name: 3 Harvard Stem Cell Institute, Cambridge, MA, USA
– name: 5 Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA, USA
– name: 1 Center for Biomedical Informatics, Harvard Medical School, Boston, MA, USA
– name: 4 Center for Regenerative Medicine, Massachusetts General Hospital, Boston, MA, USA
– name: 2 Hematology/Oncology Program, Children's Hospital, Boston, MA, USA
Author_xml – sequence: 1
  givenname: Peter V
  surname: Kharchenko
  fullname: Kharchenko, Peter V
  email: peter.kharchenko@post.harvard.edu
  organization: Center for Biomedical Informatics, Harvard Medical School, Hematology/Oncology Program, Children's Hospital, Harvard Stem Cell Institute
– sequence: 2
  givenname: Lev
  surname: Silberstein
  fullname: Silberstein, Lev
  organization: Harvard Stem Cell Institute, Center for Regenerative Medicine, Massachusetts General Hospital, Department of Stem Cell and Regenerative Biology, Harvard University
– sequence: 3
  givenname: David T
  surname: Scadden
  fullname: Scadden, David T
  organization: Harvard Stem Cell Institute, Center for Regenerative Medicine, Massachusetts General Hospital, Department of Stem Cell and Regenerative Biology, Harvard University
BackLink https://www.ncbi.nlm.nih.gov/pubmed/24836921$$D View this record in MEDLINE/PubMed
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– reference: McDavidABioinformatics2013294614671:CAS:528:DC%2BC3sXis1OjsLs%3D10.1093/bioinformatics/bts714
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– reference: MolinerAEnforsPIbanezCFAndangMStem Cells Dev.2008172332431:CAS:528:DC%2BD1cXltlSmsrk%3D10.1089/scd.2007.0211
– reference: DengQRamskoldDReiniusBSandbergRScience20143431931961:CAS:528:DC%2BC2cXktVykug%3D%3D10.1126/science.1245316
– reference: HashimshonyTWagnerFSherNYanaiICell Reports201226666731:CAS:528:DC%2BC38XhsFSmsL3J10.1016/j.celrep.2012.08.003
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Snippet A method to model expression variability in single-cell RNA-seq measurements and thus to improve subsequent data analysis. Single-cell data provide a means to...
Single-cell data provide a means to dissect the composition of complex tissues and specialized cellular environments. However, the analysis of such...
Single-cell data provides means to dissect the composition of complex tissues and specialized cellular environments. However, the analysis of such measurements...
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631/114/2415
631/1647/2217/2218
631/208/212/2019
Algorithms
Analysis
Bayes Theorem
Bayesian analysis
Bayesian statistical decision theory
Bioinformatics
Biological Microscopy
Biological Techniques
Biomedical Engineering/Biotechnology
brief-communication
Cell differentiation
Cellular biology
Gene expression
Gene Expression Profiling - methods
Life Sciences
Oligonucleotide Array Sequence Analysis
Physiological aspects
Protein expression
Proteomics
Ribonucleic acid
RNA
Sequence Analysis, RNA - methods
Single-Cell Analysis - methods
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