So many correlated tests, so little time!: Rapid adjustment of P values for multiple correlated tests

被引:354
作者
Conneely, Karen N.
Boehnke, Michael
机构
[1] Emory Univ, Sch Med, Dept Human Genet, Atlanta, GA 30322 USA
[2] Univ Michigan, Ctr Stat Genet, Dept Biostat, Ann Arbor, MI 48109 USA
关键词
SINGLE-NUCLEOTIDE POLYMORPHISMS; CLINICAL-TRIALS; ASSOCIATION; GENES; DISTRIBUTIONS; PROBABILITIES; COMPUTATION; SIMULATION; DISEASE;
D O I
10.1086/522036
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Contemporary genetic association studies may test hundreds of thousands of genetic variants for association, often with multiple binary and continuous traits or under more than one model of inheritance. Many of these association tests may be correlated with one another because of linkage disequilibrium between nearby markers and correlation between traits and models. Permutation tests and simulation-based methods are often employed to adjust groups of correlated tests for multiple testing, since conventional methods such as Bonferroni correction are overly conservative when tests are correlated. We present here a method of computing P values adjusted for correlated tests (P-ACT) that attains the accuracy of permutation or simulation-based tests in much less computation time, and we show that our method applies to many common association tests that are based on multiple traits, markers, and genetic models. Simulation demonstrates that P-ACT attains the power of permutation testing and provides a valid adjustment for hundreds of correlated association tests. In data analyzed as part of the Finland-United States Investigation of NIDDM Genetics (FUSION) study, we observe a near one-to-one relationship (r(2) > .999) between P-ACT and the corresponding permutation-based P values, achieving the same precision as permutation testing but thousands of times faster.
引用
收藏
页码:1158 / 1168
页数:11
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