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Shimmer: detection of genetic alterations in tumors using next-generation sequence data

Motivation: Extensive DNA sequencing of tumor and matched normal samples using exome and whole-genome sequencing technologies has enabled the discovery of recurrent genetic alterations in cancer cells, but variability in stromal contamination and subclonal heterogeneity still present a severe challe...

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Detalhes bibliográficos
Main Authors: Hansen, Nancy F., Gartner, Jared J., Mei, Lan, Samuels, Yardena, Mullikin, James C.
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2013
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3673219/
https://ncbi.nlm.nih.gov/pubmed/23620360
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btt183
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