Somatic variant calling from single-cell DNA sequencing data

Single-cell sequencing has gained popularity in recent years. Despite its numerous applications, single-cell DNA sequencing data is highly error-prone due to technical biases arising from uneven sequencing coverage, allelic dropout, and amplification error. With these artifacts, the identification o...

Descripción completa

Detalles Bibliográficos
Autores principales: Valecha, Monica, Posada, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Research Network of Computational and Structural Biotechnology 2022
Materias:
Mini Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9218383/
https://www.ncbi.nlm.nih.gov/pubmed/35782734
http://dx.doi.org/10.1016/j.csbj.2022.06.013

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9218383/
https://www.ncbi.nlm.nih.gov/pubmed/35782734
http://dx.doi.org/10.1016/j.csbj.2022.06.013

Ejemplares similares