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chromVAR: inferring transcription-factor-associated accessibility from single-cell epigenomic data

chromVAR: inferring transcription-factor-associated accessibility from single-cell epigenomic data

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5623146

chromVAR: inferring transcription-factor-associated accessibility from single-cell epigenomic data

About this item

Full title

chromVAR: inferring transcription-factor-associated accessibility from single-cell epigenomic data

Publisher

London: Nature Publishing Group UK

Journal title

Nature methods, 2017-10, Vol.14 (10), p.975-978

Language

English

Formats

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

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 va...

Alternative Titles

Full title

chromVAR: inferring transcription-factor-associated accessibility from single-cell epigenomic data

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5623146

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5623146

Other Identifiers

ISSN

1548-7091

E-ISSN

1548-7105

DOI

10.1038/nmeth.4401

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