Nonlinear tests for genomewide association studies

被引:13
作者
Zhao, Jinying
Jin, Li
Xiong, Momiao
机构
[1] Univ Texas, Hlth Sci Ctr, Ctr Human Genet, Sch Publ Hlth, Houston, TX 77030 USA
[2] Fudan Univ, Sch Life Sci, Lab Theoret Syst Biol, Shanghai 200433, Peoples R China
[3] CAS, SIBS, Partner Inst Computat Biol, CAS MPG, Shanghai 200031, Peoples R China
关键词
LINKAGE DISEQUILIBRIUM TESTS; WIDE ASSOCIATION; HAPLOTYPE; SCHIZOPHRENIA; POPULATION; DISEASES; FUTURE; SNP;
D O I
10.1534/genetics.106.060491
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
As millions of single-nucleotide polymorphisms (SNPs) have been identified and high-throughput genotyping technologies have been rapidly developed, large-scale genomewide association studies are soon within reach. However, since a genomewide association Study involves a large number of SNPs it is therefore nearly impossible to ensure a genomewide significance level of 0.05 using the available statistics, although the multiple-test problems can be alleviated, but not sufficiently, by the use of tagging SNPs. One strategy to circumvent the multiple-test problem associated with genome-wide association tests is to develop novel test statistics with high power. In this report, we introduce several nonlinear tests, which are based on nonlinear transformation of allele or haplotype frequencies. We investigate the power of the nonlinear test statistics and demonstrate that under certain conditions, some nonlinear test statistics have much higher power than the standard chi(2)-test statistic. Type I error rates of the nonlinear tests are validated using simulation studies. We also show that a class of similarity measure-based test statistics is based on the quadratic function of allele or haplotype frequencies, and thus they belong to nonlinear tests. To evaluate their performance, the nonlinear test statistics are also applied to three real data sets. Our study shows that nonlinear test statistics have great potential in association studies of complex diseases.
引用
收藏
页码:1529 / 1538
页数:10
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