VarScan 2: Somatic mutation and copy number alteration discovery in cancer by exome sequencing

Cancer is a disease driven by genetic variation and mutation. Exome sequencing can be utilized for discovering these variants and mutations across hundreds of tumors. Here we present an analysis tool, VarScan 2, for the detection of somatic mutations and copy number alterations (CNAs) in exome data...

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Bibliografski detalji
Glavni autori: Koboldt, Daniel C., Zhang, Qunyuan, Larson, David E., Shen, Dong, McLellan, Michael D., Lin, Ling, Miller, Christopher A., Mardis, Elaine R., Ding, Li, Wilson, Richard K.
Format: Artigo
Jezik:Inglês
Izdano: Cold Spring Harbor Laboratory Press 2012
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Resource
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3290792/
https://ncbi.nlm.nih.gov/pubmed/22300766
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/gr.129684.111
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