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The relationship between imputation error and statistical power in genetic association studies in diverse populations.

机译:不同人群遗传关联研究中归因误差与统计能力之间的关系。

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Genotype-imputation methods provide an essential technique for high-resolution genome-wide association (GWA) studies with millions of single-nucleotide polymorphisms. For optimal design and interpretation of imputation-based GWA studies, it is important to understand the connection between imputation error and power to detect associations at imputed markers. Here, using a 2x3 chi-square test, we describe a relationship between genotype-imputation error rates and the sample-size inflation required for achieving statistical power at an imputed marker equal to that obtained if genotypes at the marker were known with certainty. Surprisingly, typical imputation error rates (approximately 2%-6%) lead to a large increase in the required sample size (approximately 10%-60%), and in some African populations whose genotypes are particularly difficult to impute, the required sample-size increase is as high as approximately 30%-150%. In most populations, each 1% increase in imputation error leads to an increase of approximately 5%-13% in the sample size required for maintaining power. These results imply that in GWA sample-size calculations investigators will need to account for a potentially considerable loss of power from even low levels of imputation error and that development of additional genomic resources that decrease imputation error will translate into substantial reduction in the sample sizes needed for imputation-based detection of the variants that underlie complex human diseases.
机译:基因型输入方法为具有数百万个单核苷酸多态性的高分辨率全基因组关联(GWA)研究提供了一种必不可少的技术。对于基于插补的GWA研究的最佳设计和解释,了解插补误差与检测插补标记关联的能力之间的联系非常重要。在这里,我们使用2x3卡方检验来描述基因型输入错误率与在推定标记上获得统计功效所需的样本量膨胀之间的关系,该确定能力等于确定标记基因型时获得的统计功效。令人惊讶的是,典型的插补错误率(约2%-6%)导致所需样本量大幅增加(约10%-60%),在某些基因型特别难以估算的非洲人群中,所需样本尺寸增加高达大约30%-150%。在大多数人群中,插补误差每增加1%,保持功效所需的样本量就会增加大约5%-13%。这些结果表明,在GWA样本量计算中,研究人员将需要考虑即使是较低水平的插补误差也可能造成的相当大的功率损失,并且开发减少插补误差的其他基因组资源将转化为所需样本量的大幅减少。基于插值的检测方法,可以检测出人类复杂疾病的基础。

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