Gene-set association tests for next-generation sequencing data

被引:8
作者
Lee, Jaehoon [1 ]
Kim, Young Jin [2 ]
Lee, Juyoung [2 ]
Kim, Bong-Jo [2 ]
Lee, Seungyeoun [3 ]
Park, Taesung [1 ]
机构
[1] Seoul Natl Univ, Dept Stat, Seoul 151742, South Korea
[2] Korean Natl Inst Hlth, Div Struct & Funct Genom, Osong 363951, Chungchungbuk D, South Korea
[3] Sejong Univ, Dept Math & Stat, Seoul 143747, South Korea
关键词
GENOME-WIDE ASSOCIATION; CARBON-TETRACHLORIDE; COMPLEX DISEASES; RARE VARIANTS; TRAITS; HEPATOTOXICITY; POPULATION; PROFILES; PATHWAY; MICE;
D O I
10.1093/bioinformatics/btw429
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation: Recently, many methods have been developed for conducting rare-variant association studies for sequencing data. These methods have primarily been based on gene-level associations but have not been proven to be as effective as expected. Gene-set-level tests have shown great advantages over gene-level tests in terms of power and robustness, because complex diseases are often caused by multiple genes that comprise of biological gene sets. Results: Here, we propose several novel gene-set tests that employ rapid and efficient dimensionality reduction. The performance of these tests was investigated using extensive simulations and application to 1058 whole-exome sequences from a Korean population. We identified some known pathways and novel pathways whose rare or common variants are associated with elevated liver enzymes and replicated the results in an independent cohort.
引用
收藏
页码:611 / 619
页数:9
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