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chromVAR: inferring transcription-factor-associated accessibility from single-cell epigenomic data
by
Schep, Alicia N
, Greenleaf, William J
, Wu, Beijing
, Buenrostro, Jason D
in
45
/ 45/23
/ 631/114/2114
/ 631/114/2404
/ 631/114/2785
/ 631/114/794
/ Accessibility
/ Algorithms
/ Animals
/ Annotations
/ B cells
/ Bias
/ Binding sites
/ Bioinformatics
/ Biological Microscopy
/ Biological Techniques
/ Biomedical Engineering/Biotechnology
/ brief-communication
/ Cell Line
/ Chromatin
/ Clustering
/ Data analysis
/ Data processing
/ DNA sequencing
/ Epigenomics - methods
/ Gene expression
/ Gene Expression Regulation
/ Genetic aspects
/ Leukemia
/ Life Sciences
/ Proteomics
/ Sequence Analysis, DNA - methods
/ Software
/ Stem cells
/ Transcription factors
/ Transcription Factors - metabolism
2017
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chromVAR: inferring transcription-factor-associated accessibility from single-cell epigenomic data
by
Schep, Alicia N
, Greenleaf, William J
, Wu, Beijing
, Buenrostro, Jason D
in
45
/ 45/23
/ 631/114/2114
/ 631/114/2404
/ 631/114/2785
/ 631/114/794
/ Accessibility
/ Algorithms
/ Animals
/ Annotations
/ B cells
/ Bias
/ Binding sites
/ Bioinformatics
/ Biological Microscopy
/ Biological Techniques
/ Biomedical Engineering/Biotechnology
/ brief-communication
/ Cell Line
/ Chromatin
/ Clustering
/ Data analysis
/ Data processing
/ DNA sequencing
/ Epigenomics - methods
/ Gene expression
/ Gene Expression Regulation
/ Genetic aspects
/ Leukemia
/ Life Sciences
/ Proteomics
/ Sequence Analysis, DNA - methods
/ Software
/ Stem cells
/ Transcription factors
/ Transcription Factors - metabolism
2017
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chromVAR: inferring transcription-factor-associated accessibility from single-cell epigenomic data
by
Schep, Alicia N
, Greenleaf, William J
, Wu, Beijing
, Buenrostro, Jason D
in
45
/ 45/23
/ 631/114/2114
/ 631/114/2404
/ 631/114/2785
/ 631/114/794
/ Accessibility
/ Algorithms
/ Animals
/ Annotations
/ B cells
/ Bias
/ Binding sites
/ Bioinformatics
/ Biological Microscopy
/ Biological Techniques
/ Biomedical Engineering/Biotechnology
/ brief-communication
/ Cell Line
/ Chromatin
/ Clustering
/ Data analysis
/ Data processing
/ DNA sequencing
/ Epigenomics - methods
/ Gene expression
/ Gene Expression Regulation
/ Genetic aspects
/ Leukemia
/ Life Sciences
/ Proteomics
/ Sequence Analysis, DNA - methods
/ Software
/ Stem cells
/ Transcription factors
/ Transcription Factors - metabolism
2017
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chromVAR: inferring transcription-factor-associated accessibility from single-cell epigenomic data
Journal Article
chromVAR: inferring transcription-factor-associated accessibility from single-cell epigenomic data
2017
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Overview
ChromVar infers transcription-factor-associated accessibility from low-coverage or single-cell chromatin-accessibility data, thus enabling the clustering of cells and analysis of regulatory sequence motifs from sparse data sets.
Single-cell ATAC-seq (scATAC) yields sparse data that make conventional analysis challenging. We developed chromVAR (
http://www.github.com/GreenleafLab/chromVAR
), an R package for analyzing sparse chromatin-accessibility data by estimating gain or loss of accessibility within peaks sharing the same motif or annotation while controlling for technical biases. chromVAR enables accurate clustering of scATAC-seq profiles and characterization of known and
de novo
sequence motifs associated with variation in chromatin accessibility.
Publisher
Nature Publishing Group UK,Nature Publishing Group
Subject
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