Office of Biostatistics Research, National Heart, Lung and Blood Institute, Bethesda, 6701 Rockledge Dr, MSC 7938, Maryland 20892, USA.
BMC Genet. 2005 Dec 30;6 Suppl 1(Suppl 1):S93. doi: 10.1186/1471-2156-6-S1-S93.
We studied several methods for selecting single-nucleotide polymorphisms (SNPs) in a disease association study. Two major categories for analytical strategy are the univariate and the set selection approaches. The univariate approach evaluates each SNP marker one at a time, while the set selection approach tests disease association of a set of SNP markers simultaneously. We examined various test statistics that can be utilized in testing disease association and also reviewed several multiple testing procedures that can properly control the family-wise error rates when the univariate approach is applied to multiple markers. The set association methods were then briefly reviewed. Finally, we applied these methods to the data from Collaborative Study on the Genetics of Alcoholism (COGA).
我们研究了几种在疾病关联研究中选择单核苷酸多态性(SNP)的方法。分析策略主要有两类:单变量方法和集合选择方法。单变量方法每次评估一个 SNP 标记,而集合选择方法则同时测试一组 SNP 标记的疾病关联。我们研究了可以用于检测疾病关联的各种检验统计量,并回顾了几种多重检验程序,当应用于多个标记时,这些程序可以正确控制总体错误率。然后简要回顾了集合关联方法。最后,我们将这些方法应用于来自酒精中毒遗传学合作研究(COGA)的数据。