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EpiScanpy: integrated single-cell epigenomic analysis

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 near...

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Autores principales: Danese, Anna, Richter, Maria L., Chaichoompu, Kridsadakorn, Fischer, David S., Theis, Fabian J., Colomé-Tatché, Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8410937/
https://www.ncbi.nlm.nih.gov/pubmed/34471111
http://dx.doi.org/10.1038/s41467-021-25131-3
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author Danese, Anna
Richter, Maria L.
Chaichoompu, Kridsadakorn
Fischer, David S.
Theis, Fabian J.
Colomé-Tatché, Maria
author_facet Danese, Anna
Richter, Maria L.
Chaichoompu, Kridsadakorn
Fischer, David S.
Theis, Fabian J.
Colomé-Tatché, Maria
author_sort Danese, Anna
collection PubMed
description 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.
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spelling pubmed-84109372021-09-22 EpiScanpy: integrated single-cell epigenomic analysis Danese, Anna Richter, Maria L. Chaichoompu, Kridsadakorn Fischer, David S. Theis, Fabian J. Colomé-Tatché, Maria Nat Commun Article 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. Nature Publishing Group UK 2021-09-01 /pmc/articles/PMC8410937/ /pubmed/34471111 http://dx.doi.org/10.1038/s41467-021-25131-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Danese, Anna
Richter, Maria L.
Chaichoompu, Kridsadakorn
Fischer, David S.
Theis, Fabian J.
Colomé-Tatché, Maria
EpiScanpy: integrated single-cell epigenomic analysis
title EpiScanpy: integrated single-cell epigenomic analysis
title_full EpiScanpy: integrated single-cell epigenomic analysis
title_fullStr EpiScanpy: integrated single-cell epigenomic analysis
title_full_unstemmed EpiScanpy: integrated single-cell epigenomic analysis
title_short EpiScanpy: integrated single-cell epigenomic analysis
title_sort episcanpy: integrated single-cell epigenomic analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8410937/
https://www.ncbi.nlm.nih.gov/pubmed/34471111
http://dx.doi.org/10.1038/s41467-021-25131-3
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