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关于遗传关联和连锁研究的平均功率。

On averaging power for genetic association and linkage studies.

作者信息

Zheng Gang, Joo Jungnam, Ganesh Santhi K, Nabel Elizabeth G, Geller Nancy L

机构信息

Office of Biostatistics Research, National Heart, Lung and Blood Institute, Bethesda, Md 20892, USA.

出版信息

Hum Hered. 2005;59(1):14-20. doi: 10.1159/000084732. Epub 2005 Mar 30.

Abstract

A power calculation is crucial in planning genetic studies. In genetic association studies, the power is often calculated using the expected number of individuals with each genotype calculated from an assumed allele frequency under Hardy-Weinberg equilibrium. Since the allele frequency is often unknown, the number of individuals with each genotype is random and so a power calculation assuming a known allele frequency may be incorrect. Ambrosius et al. recently showed that the power ignoring this randomness may lead to studies with insufficient power and proposed averaging the power due to the randomness. We extend the method of averaging power in two directions. First, for testing association in case-control studies, we use the Cochran-Armitage trend test and find that the time needed for calculating the averaged power is much reduced compared to the chi-square test with two degrees of freedom studied by Ambrosius et al. A real study is used for illustration of the method. Second, we extend the method to linkage analysis, where the number of identical-by-descent alleles shared by siblings is random. The distribution of identical-by-descent numbers depends on the underlying genetic model rather than the allele frequency. The robust test for linkage analysis is also examined using the averaged powers. We also recommend a sensitivity analysis when the true allele frequency or the number of identical-by-descent alleles is unknown.

摘要

功效计算在规划基因研究中至关重要。在基因关联研究中,功效通常是根据哈迪 - 温伯格平衡下假设的等位基因频率计算出的每种基因型个体的预期数量来计算的。由于等位基因频率往往未知,每种基因型的个体数量是随机的,因此假设已知等位基因频率进行的功效计算可能不正确。安布罗修斯等人最近表明,忽略这种随机性的功效计算可能会导致研究功效不足,并提出对等位基因频率随机性导致的功效进行平均。我们从两个方向扩展了平均功效的方法。首先,对于病例对照研究中的关联性检验,我们使用 Cochr an - Armitage趋势检验,发现与安布罗修斯等人研究的自由度为2的卡方检验相比,计算平均功效所需的时间大幅减少。通过一项实际研究来说明该方法。其次,我们将该方法扩展到连锁分析,其中同胞共享的同源等位基因数量是随机的。同源等位基因数量的分布取决于潜在的遗传模型而非等位基因频率。还使用平均功效检验了连锁分析的稳健性检验。当真实等位基因频率或同源等位基因数量未知时,我们还建议进行敏感性分析。

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