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Impact of genotyping errors on the type I error rate and the power of haplotype-based association methods

机译:基因分型错误对I型错误率和基于单倍型关联方法的影响

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Background We investigated the influence of genotyping errors on the type I error rate and empirical power of two haplotype based association methods applied to candidate regions. We compared the performance of the Mantel Statistic Using Haplotype Sharing and the haplotype frequency based score test with that of the Armitage trend test. Our study is based on 1000 replication of simulated case-control data settings with 500 cases and 500 controls, respectively. One of the examined markers was set to be the disease locus with a simulated odds ratio of 3. Differential and non-differential genotyping errors were introduced following a misclassification model with varying mean error rates per locus in the range of 0.2% to 15.6%. Results We found that the type I error rate of all three test statistics hold the nominal significance level in the presence of nondifferential genotyping errors and low error rates. For high and differential error rates, the type I error rate of all three test statistics was inflated, even when genetic markers not in Hardy-Weinberg Equilibrium were removed. The empirical power of all three association test statistics remained high at around 89% to 94% when genotyping error rates were low, but decreased to 48% to 80% for high and nondifferential genotyping error rates. Conclusion Currently realistic genotyping error rates for candidate gene analysis (mean error rate per locus of 0.2%) pose no significant problem for the type I error rate as well as the power of all three investigated test statistics.
机译:背景我们研究了基因分型错误对应用于候选区域的两种基于单体型的关联方法对I型错误率和经验功效的影响。我们比较了使用单元型共享的Mantel统计量和基于单元型频率的得分测试与Armitage趋势测试的性能。我们的研究是基于模拟案例控制数据设置的1000个复制,分别具有500个案例和500个控件。被检查的标记之一是模拟比值比为3的疾病基因座。按照错误分类模型引入差异和非差异基因分型错误,每个基因座的平均错误率在0.2%至15.6%范围内变化。结果我们发现,在存在非差分基因分型错误和低错误率的情况下,所有三个测试统计数据的I型错误率均保持标称显着性水平。对于高错误率和差分错误率,即使删除了不在Hardy-Weinberg平衡中的遗传标记,也会夸大所有三个测试统计数据的I型错误率。当基因分型错误率很低时,所有三个关联检验统计数据的经验能力仍然很高,大约在89%到94%之间,但是对于高和非差异性基因分型错误率则下降到48%到80%。结论当前用于候选基因分析的现实基因分型错误率(每个基因座的平均错误率是0.2%)对I型错误率以及所有这三个调查统计数据的功效均不构成重大问题。

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