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SomaticSniper: identification of somatic point mutations in whole genome sequencing data

Motivation: The sequencing of tumors and their matched normals is frequently used to study the genetic composition of cancer. Despite this fact, there remains a dearth of available software tools designed to compare sequences in pairs of samples and identify sites that are likely to be unique to one...

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Detalhes bibliográficos
Main Authors: Larson, David E., Harris, Christopher C., Chen, Ken, Koboldt, Daniel C., Abbott, Travis E., Dooling, David J., Ley, Timothy J., Mardis, Elaine R., Wilson, Richard K., Ding, Li
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2012
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3268238/
https://ncbi.nlm.nih.gov/pubmed/22155872
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btr665
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