Troendle James F, Mills James L
Biostatistics and Bioinformatics Branch of the Division of Epidemiology, Statistics, and Prevention Research of the Eunice Kennedy Shriver National Institute of Child Health and Human Development, NIH/DHHS, Bethesda, MD 20892, USA.
Ann Hum Genet. 2011 Mar;75(2):284-91. doi: 10.1111/j.1469-1809.2010.00626.x. Epub 2010 Nov 25.
New technology for large-scale genotyping has created new challenges for statistical analysis. Correcting for multiple comparison without discarding true positive results and extending methods to triad studies are among the important problems facing statisticians. We present a one-sample permutation test for testing transmission disequilibrium hypotheses in triad studies, and show how this test can be used for multiple single nucleotide polymorphism (SNP) testing. The resulting multiple comparison procedure is shown in the case of the transmission disequilibrium test to control the familywise error. Furthermore, this procedure can handle multiple possible modes of risk inheritance per SNP. The resulting permutational procedure is shown through simulation of SNP data to be more powerful than the Bonferroni procedure when the SNPs are in linkage disequilibrium. Moreover, permutations implicitly avoid any multiple comparison correction penalties when the SNP has a rare allele. The method is illustrated by analyzing a large candidate gene study of neural tube defects and an independent study of oral clefts, where the smallest adjusted p-values using the permutation procedure are approximately half those of the Bonferroni procedure. We conclude that permutation tests are more powerful for identifying disease-associated SNPs in candidate gene studies and are useful for analysis of triad studies.
大规模基因分型的新技术给统计分析带来了新的挑战。在不丢弃真阳性结果的情况下校正多重比较以及将方法扩展到三联体研究是统计学家面临的重要问题。我们提出了一种单样本置换检验,用于在三联体研究中检验传递不平衡假设,并展示了该检验如何用于多个单核苷酸多态性(SNP)检验。在传递不平衡检验的情况下,所得的多重比较程序可控制家族性错误率。此外,该程序可以处理每个SNP多种可能的风险遗传模式。当SNP处于连锁不平衡状态时,通过对SNP数据的模拟表明,所得的置换程序比邦费罗尼程序更具功效。此外,当SNP具有罕见等位基因时,置换隐含地避免了任何多重比较校正惩罚。通过分析神经管缺陷的大型候选基因研究和唇腭裂的独立研究来说明该方法,其中使用置换程序得到的最小校正p值约为邦费罗尼程序得到的p值的一半。我们得出结论,置换检验在候选基因研究中对于识别疾病相关SNP更具功效,并且对三联体研究的分析很有用。