Fischer Christine, Beckmann Lars, Majoram Paul, te Meerman Gerard, Chang-Claude Jenny
Institute of Human Genetics, University of Heidelberg, Heidelberg, Germany.
Genet Epidemiol. 2003 Jan;24(1):68-73. doi: 10.1002/gepi.10207.
Haplotype sharing analysis was used to investigate the association of affection status with single nucleotide polymorphism (SNP) haplotypes within candidate gene 1 in one sample each from the isolated and the general population of Genetic Analysis Workshop (GAW) 12 simulated data. Gene 1 has direct influence on affection and harbors more than 70 SNPs. Haplotype sharing analysis depends heavily on previous haplotype estimation. Using GENEHUNTER haplotypes, strong evidence was found for most SNPs in the isolated population sample, thus providing evidence for an involvement of this gene, but the maximum -log(10)(p) values for the haplotype sharing statistics (HSS) test statistic did not correspond to the location of the true variant in either population. In comparison, transmission disequilibrium test (TDT) analysis showed the strongest results at the disease-causing variant in both populations, and these were outstanding in the general population. In this example, TDT analysis appears to perform better than HSS in identifying the disease-causing variant, using SNPs within a candidate gene in an outbred population. Simulations showed that the performance of HSS is hampered by closely spaced SNPs in strong linkage disequilibrium with the functional variant and by ambiguous haplotypes.
单倍型共享分析用于研究遗传分析研讨会(GAW)12模拟数据中隔离人群和普通人群各一个样本中候选基因1内单核苷酸多态性(SNP)单倍型与患病状态之间的关联。基因1对患病情况有直接影响,包含70多个SNP。单倍型共享分析在很大程度上依赖于先前的单倍型估计。使用GENEHUNTER单倍型,在隔离人群样本中的大多数SNP发现了有力证据,从而为该基因的参与提供了证据,但单倍型共享统计量(HSS)检验统计量的最大-log(10)(p)值在两个群体中均未对应到真实变异的位置。相比之下,传递不平衡检验(TDT)分析在两个群体的致病变异处显示出最强结果,且在普通人群中尤为突出。在这个例子中,使用远交群体中候选基因内的SNP,TDT分析在识别致病变异方面似乎比HSS表现更好。模拟表明,与功能变异处于强连锁不平衡状态的紧密相邻SNP以及模糊的单倍型会阻碍HSS的性能。