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epiAneufinder identifies copy number alterations from single-cell ATAC-seq data

Single-cell open chromatin profiling via scATAC-seq has become a mainstream measurement of open chromatin in single-cells. Here we present epiAneufinder, an algorithm that exploits the read count information from scATAC-seq data to extract genome-wide copy number alterations (CNAs) for individual ce...

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Autores principales: Ramakrishnan, Akshaya, Symeonidi, Aikaterini, Hanel, Patrick, Schmid, Katharina T., Richter, Maria L., Schubert, Michael, Colomé-Tatché, Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10511508/
https://www.ncbi.nlm.nih.gov/pubmed/37730813
http://dx.doi.org/10.1038/s41467-023-41076-1
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author Ramakrishnan, Akshaya
Symeonidi, Aikaterini
Hanel, Patrick
Schmid, Katharina T.
Richter, Maria L.
Schubert, Michael
Colomé-Tatché, Maria
author_facet Ramakrishnan, Akshaya
Symeonidi, Aikaterini
Hanel, Patrick
Schmid, Katharina T.
Richter, Maria L.
Schubert, Michael
Colomé-Tatché, Maria
author_sort Ramakrishnan, Akshaya
collection PubMed
description Single-cell open chromatin profiling via scATAC-seq has become a mainstream measurement of open chromatin in single-cells. Here we present epiAneufinder, an algorithm that exploits the read count information from scATAC-seq data to extract genome-wide copy number alterations (CNAs) for individual cells, allowing the study of CNA heterogeneity present in a sample at the single-cell level. Using different cancer scATAC-seq datasets, we show that epiAneufinder can identify intratumor clonal heterogeneity in populations of single cells based on their CNA profiles. We demonstrate that these profiles are concordant with the ones inferred from single-cell whole genome sequencing data for the same samples. EpiAneufinder allows the inference of single-cell CNA information from scATAC-seq data, without the need of additional experiments, unlocking a layer of genomic variation which is otherwise unexplored.
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spelling pubmed-105115082023-09-22 epiAneufinder identifies copy number alterations from single-cell ATAC-seq data Ramakrishnan, Akshaya Symeonidi, Aikaterini Hanel, Patrick Schmid, Katharina T. Richter, Maria L. Schubert, Michael Colomé-Tatché, Maria Nat Commun Article Single-cell open chromatin profiling via scATAC-seq has become a mainstream measurement of open chromatin in single-cells. Here we present epiAneufinder, an algorithm that exploits the read count information from scATAC-seq data to extract genome-wide copy number alterations (CNAs) for individual cells, allowing the study of CNA heterogeneity present in a sample at the single-cell level. Using different cancer scATAC-seq datasets, we show that epiAneufinder can identify intratumor clonal heterogeneity in populations of single cells based on their CNA profiles. We demonstrate that these profiles are concordant with the ones inferred from single-cell whole genome sequencing data for the same samples. EpiAneufinder allows the inference of single-cell CNA information from scATAC-seq data, without the need of additional experiments, unlocking a layer of genomic variation which is otherwise unexplored. Nature Publishing Group UK 2023-09-20 /pmc/articles/PMC10511508/ /pubmed/37730813 http://dx.doi.org/10.1038/s41467-023-41076-1 Text en © The Author(s) 2023 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Ramakrishnan, Akshaya
Symeonidi, Aikaterini
Hanel, Patrick
Schmid, Katharina T.
Richter, Maria L.
Schubert, Michael
Colomé-Tatché, Maria
epiAneufinder identifies copy number alterations from single-cell ATAC-seq data
title epiAneufinder identifies copy number alterations from single-cell ATAC-seq data
title_full epiAneufinder identifies copy number alterations from single-cell ATAC-seq data
title_fullStr epiAneufinder identifies copy number alterations from single-cell ATAC-seq data
title_full_unstemmed epiAneufinder identifies copy number alterations from single-cell ATAC-seq data
title_short epiAneufinder identifies copy number alterations from single-cell ATAC-seq data
title_sort epianeufinder identifies copy number alterations from single-cell atac-seq data
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10511508/
https://www.ncbi.nlm.nih.gov/pubmed/37730813
http://dx.doi.org/10.1038/s41467-023-41076-1
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