SNVMix: predicting single nucleotide variants from next-generation sequencing of tumors

Motivation: Next-generation sequencing (NGS) has enabled whole genome and transcriptome single nucleotide variant (SNV) discovery in cancer. NGS produces millions of short sequence reads that, once aligned to a reference genome sequence, can be interpreted for the presence of SNVs. Although tools ex...

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Detalhes bibliográficos
Main Authors: Goya, Rodrigo, Sun, Mark G.F., Morin, Ryan D., Leung, Gillian, Ha, Gavin, Wiegand, Kimberley C., Senz, Janine, Crisan, Anamaria, Marra, Marco A., Hirst, Martin, Huntsman, David, Murphy, Kevin P., Aparicio, Sam, Shah, Sohrab P.
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2010
Assuntos:
Original Papers
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2832826/
https://ncbi.nlm.nih.gov/pubmed/20130035
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btq040
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