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.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10511508PMC
http://dx.doi.org/10.1038/s41467-023-41076-1DOI Listing

Publication Analysis

Top Keywords

copy number
8
number alterations
8
open chromatin
8
scatac-seq data
8
single-cell
5
epianeufinder
4
epianeufinder identifies
4
identifies copy
4
alterations single-cell
4
single-cell atac-seq
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!