Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Genet Epidemiol. 2013 Nov;37(7):743-50. doi: 10.1002/gepi.21753. Epub 2013 Aug 11.
Testing for the Hardy-Weinberg equilibrium (HWE) is often used as an initial step for checking the quality of genotyping. When testing the HWE for case-control data, the impact of a potential genetic association between the marker and the disease must be controlled for otherwise the results may be biased. Li and Li [2008] proposed a likelihood ratio test (LRT) that accounts for this potential genetic association and it is more powerful than the commonly used control-only χ² test. However, the LRT is not efficient when the marker is independent of the disease, and also requires numerical optimization to calculate the test statistic. In this article, we propose a novel shrinkage test for assessing the HWE. The proposed shrinkage test yields higher statistical power than the LRT when the marker is independent of or weakly associated with the disease, and converges to the LRT when the marker is strongly associated with the disease. In addition, the proposed shrinkage test has a closed form and can be easily used to test the HWE for large datasets that result from genome-wide association studies. We compare the performance of the shrinkage test with existing methods using simulation studies, and apply the shrinkage test to a genome-wide association dataset for Alzheimer's disease.
检验 Hardy-Weinberg 平衡(HWE)通常是检查基因分型质量的初始步骤。在针对病例对照数据检验 HWE 时,必须控制标记与疾病之间潜在遗传关联的影响,否则结果可能会有偏差。Li 和 Li [2008]提出了一种似然比检验(LRT),该检验考虑了这种潜在的遗传关联,比常用的仅控制 χ²检验更有效。然而,当标记与疾病独立时,LRT 效率不高,并且还需要数值优化来计算检验统计量。在本文中,我们提出了一种新的收缩检验来评估 HWE。当标记与疾病独立或弱相关时,提出的收缩检验比 LRT 具有更高的统计功效,而当标记与疾病强相关时,它会收敛到 LRT。此外,提出的收缩检验具有封闭形式,可以很容易地用于检验源自全基因组关联研究的大型数据集的 HWE。我们使用模拟研究比较了收缩检验与现有方法的性能,并将收缩检验应用于阿尔茨海默病的全基因组关联数据集。