Cargando…
Discovering single nucleotide variants and indels from bulk and single-cell ATAC-seq
Genetic variants and de novo mutations in regulatory regions of the genome are typically discovered by whole-genome sequencing (WGS), however WGS is expensive and most WGS reads come from non-regulatory regions. The Assay for Transposase-Accessible Chromatin (ATAC-seq) generates reads from regulator...
Autores principales: | Massarat, Arya R, Sen, Arko, Jaureguy, Jeff, Tyndale, Sélène T, Fu, Yi, Erikson, Galina, McVicker, Graham |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8373110/ https://www.ncbi.nlm.nih.gov/pubmed/34313779 http://dx.doi.org/10.1093/nar/gkab621 |
Ejemplares similares
-
Comprehensive analysis of single cell ATAC-seq data with SnapATAC
por: Fang, Rongxin, et al.
Publicado: (2021) -
simATAC: a single-cell ATAC-seq simulation framework
por: Navidi, Zeinab, et al.
Publicado: (2021) -
CoRE-ATAC: A deep learning model for the functional classification of regulatory elements from single cell and bulk ATAC-seq data
por: Thibodeau, Asa, et al.
Publicado: (2021) -
Single-cell ATAC-seq: strength in numbers
por: Pott, Sebastian, et al.
Publicado: (2015) -
ATACAmp: a tool for detecting ecDNA/HSRs from bulk and single-cell ATAC-seq data
por: Cheng, Hansen, et al.
Publicado: (2023)