Cobolt: integrative analysis of multimodal single-cell sequencing data.


Journal

Genome biology
ISSN: 1474-760X
Titre abrégé: Genome Biol
Pays: England
ID NLM: 100960660

Informations de publication

Date de publication:
28 12 2021
Historique:
received: 15 07 2021
accepted: 22 11 2021
entrez: 29 12 2021
pubmed: 30 12 2021
medline: 15 3 2022
Statut: epublish

Résumé

A growing number of single-cell sequencing platforms enable joint profiling of multiple omics from the same cells. We present Cobolt, a novel method that not only allows for analyzing the data from joint-modality platforms, but provides a coherent framework for the integration of multiple datasets measured on different modalities. We demonstrate its performance on multi-modality data of gene expression and chromatin accessibility and illustrate the integration abilities of Cobolt by jointly analyzing this multi-modality data with single-cell RNA-seq and ATAC-seq datasets.

Identifiants

pubmed: 34963480
doi: 10.1186/s13059-021-02556-z
pii: 10.1186/s13059-021-02556-z
pmc: PMC8715620
doi:

Substances chimiques

Chromatin 0

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

351

Subventions

Organisme : NIMH NIH HHS
ID : U19 MH114830
Pays : United States

Informations de copyright

© 2021. The Author(s).

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Auteurs

Boying Gong (B)

Division of Biostatistics, University of California, Berkeley, Berkeley, CA, USA.

Yun Zhou (Y)

Division of Biostatistics, University of California, Berkeley, Berkeley, CA, USA.

Elizabeth Purdom (E)

Department of Statistics, University of California, Berkeley, Berkeley, CA, USA. epurdom@stat.berkeley.edu.

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