An improved burden-test pipeline for identifying associations from rare germline and somatic variants

BACKGROUND: Identifying rare germline and somatic variants associated with cancer progression is an important research topic in cancer genomics. Although many approaches are proposed for rare variant association study, they are not fit for cancer sequencing data due to multiple issues, such as overl...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:BMC Genomics
Egile Nagusiak: Geng, Yu, Zhao, Zhongmeng, Zhang, Xuanping, Wang, Wenke, Cui, Xingjian, Ye, Kai, Xiao, Xiao, Wang, Jiayin
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: BioMed Central 2017
Gaiak:
Research
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC5657102/
https://ncbi.nlm.nih.gov/pubmed/29513197
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12864-017-4133-4
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