Anaconda: AN automated pipeline for somatic COpy Number variation Detection and Annotation from tumor exome sequencing data

BACKGROUND: Copy number variations (CNVs) are the main genetic structural variations in cancer genome. Detecting CNVs in genetic exome region is efficient and cost-effective in identifying cancer associated genes. Many tools had been developed accordingly and yet these tools lack of reliability beca...

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Detalhes bibliográficos
Publicado no:BMC Bioinformatics
Main Authors: Gao, Jianing, Wan, Changlin, Zhang, Huan, Li, Ao, Zang, Qiguang, Ban, Rongjun, Ali, Asim, Yu, Zhenghua, Shi, Qinghua, Jiang, Xiaohua, Zhang, Yuanwei
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2017
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Software
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5627484/
https://ncbi.nlm.nih.gov/pubmed/28974218
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-017-1833-3
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