Phylovar: toward scalable phylogeny-aware inference of single-nucleotide variations from single-cell DNA sequencing data

MOTIVATION: Single-nucleotide variants (SNVs) are the most common variations in the human genome. Recently developed methods for SNV detection from single-cell DNA sequencing data, such as SCI [Formula: see text] and scVILP, leverage the evolutionary history of the cells to overcome the technical er...

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Detalles Bibliográficos
Autores principales: Edrisi, Mohammadamin, Valecha, Monica V, Chowdary, Sunkara B V, Robledo, Sergio, Ogilvie, Huw A, Posada, David, Zafar, Hamim, Nakhleh, Luay
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
ISCB/Ismb 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9235480/
https://www.ncbi.nlm.nih.gov/pubmed/35758771
http://dx.doi.org/10.1093/bioinformatics/btac254

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9235480/
https://www.ncbi.nlm.nih.gov/pubmed/35758771
http://dx.doi.org/10.1093/bioinformatics/btac254

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