Use of deep whole-genome sequencing data to identify structure risk variants in breast cancer susceptibility genes

Functional disruptions of susceptibility genes by large genomic structure variant (SV) deletions in germlines are known to be associated with cancer risk. However, few studies have been conducted to systematically search for SV deletions in breast cancer susceptibility genes. We analysed deep (> ...

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Detalhes bibliográficos
Publicado no:Hum Mol Genet
Main Authors: Guo, Xingyi, Shi, Jiajun, Cai, Qiuyin, Shu, Xiao-Ou, He, Jing, Wen, Wanqing, Allen, Jamie, Pharoah, Paul, Dunning, Alison, Hunter, David J, Kraft, Peter, Easton, Douglas F, Zheng, Wei, Long, Jirong
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2018
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Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6454518/
https://ncbi.nlm.nih.gov/pubmed/29325031
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddy005
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