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...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: 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.
Formato: Artigo
Idioma:Inglês
Publicado em: Cold Spring Harbor Laboratory Press 2012
Assuntos:
Resource
Acesso em linha: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
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados