EpiScanpy: integrated single-cell epigenomic analysis.


Journal

Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555

Informations de publication

Date de publication:
01 09 2021
Historique:
received: 30 08 2020
accepted: 22 07 2021
entrez: 2 9 2021
pubmed: 3 9 2021
medline: 21 9 2021
Statut: epublish

Résumé

EpiScanpy is a toolkit for the analysis of single-cell epigenomic data, namely single-cell DNA methylation and single-cell ATAC-seq data. To address the modality specific challenges from epigenomics data, epiScanpy quantifies the epigenome using multiple feature space constructions and builds a nearest neighbour graph using epigenomic distance between cells. EpiScanpy makes the many existing scRNA-seq workflows from scanpy available to large-scale single-cell data from other -omics modalities, including methods for common clustering, dimension reduction, cell type identification and trajectory learning techniques, as well as an atlas integration tool for scATAC-seq datasets. The toolkit also features numerous useful downstream functions, such as differential methylation and differential openness calling, mapping epigenomic features of interest to their nearest gene, or constructing gene activity matrices using chromatin openness. We successfully benchmark epiScanpy against other scATAC-seq analysis tools and show its outperformance at discriminating cell types.

Identifiants

pubmed: 34471111
doi: 10.1038/s41467-021-25131-3
pii: 10.1038/s41467-021-25131-3
pmc: PMC8410937
doi:

Substances chimiques

Chromatin 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

5228

Informations de copyright

© 2021. The Author(s).

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Auteurs

Anna Danese (A)

Institute of Computational Biology, Helmholtz Zentrum München, German Research Center for Environmental Health, Neuherberg, Germany.

Maria L Richter (ML)

Institute of Computational Biology, Helmholtz Zentrum München, German Research Center for Environmental Health, Neuherberg, Germany.

Kridsadakorn Chaichoompu (K)

Institute of Computational Biology, Helmholtz Zentrum München, German Research Center for Environmental Health, Neuherberg, Germany.

David S Fischer (DS)

Institute of Computational Biology, Helmholtz Zentrum München, German Research Center for Environmental Health, Neuherberg, Germany.
TUM School of Life Sciences Weihenstephan, Technical University of Munich, Freising, Germany.

Fabian J Theis (FJ)

Institute of Computational Biology, Helmholtz Zentrum München, German Research Center for Environmental Health, Neuherberg, Germany. fabian.theis@helmholtz-muenchen.de.
TUM School of Life Sciences Weihenstephan, Technical University of Munich, Freising, Germany. fabian.theis@helmholtz-muenchen.de.
Department of Mathematics, Technical University of Munich, Garching, Germany. fabian.theis@helmholtz-muenchen.de.

Maria Colomé-Tatché (M)

Institute of Computational Biology, Helmholtz Zentrum München, German Research Center for Environmental Health, Neuherberg, Germany. maria.colome@bmc.med.lmu.de.
TUM School of Life Sciences Weihenstephan, Technical University of Munich, Freising, Germany. maria.colome@bmc.med.lmu.de.
Biomedical Center (BMC), Physiological Chemistry, Faculty of Medicine, LMU Munich, Planegg-Martinsried, Germany. maria.colome@bmc.med.lmu.de.

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