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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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Bibliografski detalji
Glavni autori: Hansen, Nancy F., Gartner, Jared J., Mei, Lan, Samuels, Yardena, Mullikin, James C.
Format: Artigo
Jezik:Inglês
Izdano: Oxford University Press 2013
Teme:
Online pristup: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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