Integrating germline and somatic genetics to identify genes associated with lung cancer

被引:2
|
作者
Pattee, Jack [1 ]
Zhan, Xiaowei [2 ]
Xiao, Guanghua [2 ]
Pan, Wei [1 ]
机构
[1] Univ Minnesota, Sch Publ Hlth, Div Biostat, Minneapolis, MN 55455 USA
[2] Univ Texas Southwestern Med Ctr Dallas, Dept Clin Sci, Quantitat Biomed Res Ctr, Dallas, TX 75390 USA
关键词
aSPU test; eQTL; PrediXcan; SSU test; sum test; TWAS; WIDE ASSOCIATION; EXPRESSION; POWERFUL; ARCHITECTURE; IMPUTATION; SELECTION; TRIM31; RISK; EQTL;
D O I
10.1002/gepi.22275
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Genome-wide association studies (GWAS) have successfully identified many genetic variants associated with complex traits. However, GWAS experience power issues, resulting in the failure to detect certain associated variants. Additionally, GWAS are often unable to parse the biological mechanisms of driving associations. An existing gene-based association test framework, Transcriptome-Wide Association Studies (TWAS), leverages expression quantitative trait loci data to increase the power of association tests and illuminate the biological mechanisms by which genetic variants modulate complex traits. We extend the TWAS methodology to incorporate somatic information from tumors. By integrating germline and somatic data we are able to leverage information from the nuanced somatic landscape of tumors. Thus we can augment the power of TWAS-type tests to detect germline genetic variants associated with cancer phenotypes. We use somatic and germline data on lung adenocarcinomas from The Cancer Genome Atlas in conjunction with a meta-analyzed lung cancer GWAS to identify novel genes associated with lung cancer.
引用
收藏
页码:233 / 247
页数:15
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