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Detecting rare functional variants using a wavelet-based test on quantitative and qualitative traits

机译:使用基于小波的定量和定性特征测试来检测稀有功能变异

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We conducted a genome-wide association study on the Genetic Analysis Workshop 17 simulated unrelated individuals data using a multilocus score test based on wavelet transformation that we proposed recently. Wavelet transformation is an advanced smoothing technique, whereas the currently popular collapsing methods are the simplest way to smooth multilocus genotypes. The wavelet-based test suppresses noise from the data more effectively, which results in lower type I error rates. We chose a level-dependent threshold for the wavelet-based test to suppress the optimal amount of noise according to the data. We propose several remedies to reduce the inflated type I error rate: using a window of fixed size rather than a gene; using the Bonferroni correction rather than comparing to the maxima of test values for multiple testing corrections; and removing the influence of other factors by using residuals for the association test. A wavelet-based test can detect multiple rare functional variants. Type I error rates can be controlled using the wavelet-based test combined with the mentioned remedies.
机译:我们在遗传分析研讨会17上进行了全基因组关联研究,使用最近提出的基于小波变换的多位点得分测试,对不相关的个​​人数据进行了模拟。小波变换是一种先进的平滑技术,而当前流行的折叠方法是平滑多基因座基因型的最简单方法。基于小波的测试可以更有效地抑制数据中的噪声,从而降低I型错误率。我们为基于小波的测试选择了与水平相关的阈值,以根据数据抑制最佳噪声量。我们提出了几种减少I型错误率的方法:使用固定大小的窗口而不是基因;使用Bonferroni校正,而不是与多个测试校正的测试值最大值进行比较;并通过使用残差进行关联测试来消除其他因素的影响。基于小波的测试可以检测多种罕见的功能变异。可以使用基于小波的测试结合上述补救措施来控制I型错误率。

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