Quantitative Trait Loci Identification by Estimating the Genetic Model based on the Extremal Samples

被引:0
|
作者
Yang, Zining [1 ]
Yang, Yaning [1 ]
Xu, Xu Steven [2 ]
Yuan, Min [3 ]
机构
[1] Univ Sci & Technol China, Dept Stat & Finance, Hefei 230026, Peoples R China
[2] Genmab US Inc, Princeton, NJ 08540 USA
[3] Anhui Med Univ, Ctr Data Sci Hlth, Sch Publ Hlth Adm, Hefei 230032, Peoples R China
关键词
Genetic association studies; quantitative trait loci; extreme samples; genetic model selection; hardy-weinberg disequilibrium; maximin efficiency robust test; HARDY-WEINBERG; ASSOCIATION; DISEQUILIBRIUM; SELECTION; DISEASE; TESTS;
D O I
10.2174/1389202922666210625161602
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: In genetic association studies with quantitative trait loci (QTL), the association between a candidate genetic marker and the trait of interest is commonly examined by the omnibus F test or by the t-test corresponding to a given genetic model or mode of inheritance. It is known that the t-test with a correct model specification is more powerful than the F test. However, since the underlying genetic model is rarely known in practice, the use of a model-specific t-test may incur substantial power loss. Robust-efficient tests, such as the Maximin Efficiency Robust Test (MERT) and MAX3 have been proposed in the literature. Methods: In this paper, we propose a novel two-step robust-efficient approach, namely, the genetic model selection (GMS) method for quantitative trait analysis. GMS selects a genetic model by testing Hardy-Weinberg disequilibrium (HWD) with extremal samples of the population in the first step and then applies the corresponding genetic model-specific t-test in the second step. Results: Simulations show that GMS is not only more efficient than MERT and MAX3, but also has comparable power to the optimal t-test when the genetic model is known. Conclusion: Application to the data from Alzheimer's Disease Neuroimaging Initiative (ADNI) cohort demonstrates that the proposed approach can identify meaningful biological SNPs on chromosome 19.
引用
收藏
页码:363 / 372
页数:10
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