CScape-somatic: distinguishing driver and passenger point mutations in the cancer genome

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MOTIVATION: Next-generation sequencing technologies have accelerated the discovery of single nucleotide variants in the human genome, stimulating the development of predictors for classifying which of these variants are likely functional in disease, and which neutral. Recently, we proposed CScape, a...

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Detalles Bibliográficos
Autores principales: Rogers, Mark F, Gaunt, Tom R, Campbell, Colin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Original Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7320610/
https://www.ncbi.nlm.nih.gov/pubmed/32282885
http://dx.doi.org/10.1093/bioinformatics/btaa242

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