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Power and sample size calculations in the presence of phenotype errors for case/control genetic association studies

机译:在存在表型错误的情况下进行功效和样本量计算用于病例/对照遗传关联研究

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摘要

BackgroundPhenotype error causes reduction in power to detect genetic association. We present a quantification of phenotype error, also known as diagnostic error, on power and sample size calculations for case-control genetic association studies between a marker locus and a disease phenotype. We consider the classic Pearson chi-square test for independence as our test of genetic association. To determine asymptotic power analytically, we compute the distribution's non-centrality parameter, which is a function of the case and control sample sizes, genotype frequencies, disease prevalence, and phenotype misclassification probabilities. We derive the non-centrality parameter in the presence of phenotype errors and equivalent formulas for misclassification cost (the percentage increase in minimum sample size needed to maintain constant asymptotic power at a fixed significance level for each percentage increase in a given misclassification parameter). We use a linear Taylor Series approximation for the cost of phenotype misclassification to determine lower bounds for the relative costs of misclassifying a true affected (respectively, unaffected) as a control (respectively, case). Power is verified by computer simulation.
机译:背景表型错误导致检测遗传关联的能力降低。我们提出了关于功率和样本量计算的表型错误(也称为诊断错误)的量化,用于标记基因座和疾病表型之间的病例对照遗传关联研究。我们将经典的独立性的Pearson卡方检验视为我们的遗传关联检验。为了通过分析确定渐近能力,我们计算分布的非中心性参数,该参数是病例的函数,并控制样本大小,基因型频率,疾病患病率和表型错误分类概率。我们在存在表型错误和等效公式的情况下得出错误分类成本的非中心性参数(对于给定错误分类参数中的每个百分比增长,将最小渐进样本量保持恒定的渐近幂以固定的显着水平所需的最小样本大小的百分比增加)。对于表型分类错误的成本,我们使用线性泰勒级数逼近来确定将实际受影响(分别为未受影响)作为对照(分别为案例)的相对成本的下限。功率通过计算机仿真验证。

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