An efficient family-based association test using multiple markers

被引:28
|
作者
Xu, Xin
Rakovski, Cyril
Xu, Xiping
Laird, Nan
机构
[1] Harvard Univ, Sch Publ Hlth, Program Populat Genet, Boston, MA 02115 USA
[2] Harvard Univ, Sch Publ Hlth, Dept Biostat, Boston, MA 02115 USA
[3] Univ Illinois, Sch Publ Hlth, Div Epidemiol & Biostat, Chicago, IL USA
关键词
multi-marker family-based association; FBAT;
D O I
10.1002/gepi.20174
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
In genetic association studies, multiple markers are usually employed to cover a genomic region of interest for localizing a trait locus. In this report, we propose a novel multi-marker family-based association test (T-LC) that linearly combines the single-marker test statistics using data-driven weights. We examine the type-I error rate in a numerical study and compare its power to identify a common trait locus using tag single nucleotide polymorphisms (SNPs) within the same haplotype block that the trait locus resides with three competing tests including a global haplotype test (T-H), a multi-marker test similar to the Hotelling-T-2 test for the population-based data (T-MM), and a single-marker test with Bonferroni's correction for multiple testing (T-B). The type-I error rate of T-LC is well maintained in our numeric study. In all the scenarios we examined, T-LC is the most powerful, followed by T-B. T-MM and T-H are the poorest. T-H and T-MM have essentially the same power when parents are available. However, when both parents are missing, T-MM is substantially more powerful than TH. We also apply this new test on a data set from a previous association study on nicotine dependence.
引用
收藏
页码:620 / 626
页数:7
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