Detecting somatic point mutations in cancer genome sequencing data: a comparison of mutation callers

BACKGROUND: Driven by high throughput next generation sequencing technologies and the pressing need to decipher cancer genomes, computational approaches for detecting somatic single nucleotide variants (sSNVs) have undergone dramatic improvements during the past 2 years. The recently developed tools...

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Bibliographic Details
Main Authors: Wang, Qingguo, Jia, Peilin, Li, Fei, Chen, Haiquan, Ji, Hongbin, Hucks, Donald, Dahlman, Kimberly Brown, Pao, William, Zhao, Zhongming
Format: Artigo
Language:Inglês
Published: BioMed Central 2013
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Research
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC3971343/
https://ncbi.nlm.nih.gov/pubmed/24112718
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/gm495
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