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Relationship Between Genomic Distance-Based Regression and Kernel Machine Regression for Multi-Marker Association Testing

机译:用于多标记关联测试的基于基因组距离的回归与核机器回归之间的关系

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To detect genetic association with common and complex diseases, two powerful yet quite different multimarker association tests have been proposed, genomic distance-based regression (GDBR) (Wessel and Schork [2006] Am J Hum Genet 79:821-833) and kernel machine regression (KMR) (Kwee et al. [2008] Am J Hum Genet 82:386-397; Wu et al. [2010] Am J Hum Genet 86:929-942). GDBR is based on relating a multimarker similarity metric for a group of subjects to variation in their trait values, while KMR is based on nonparametric estimates of the effects of the multiple markers on the trait through a kernel function or kernel matrix. Since the two approaches are both powerful and general, but appear quite different, it is important to know their specific relationships. In this report, we show that, under the condition that there is no other covariate, there is a striking correspondence between the two approaches for a quantitative or a binary trait: if the same positive semi-definite matrix is used as the centered similarity matrix in GDBR and as the kernel matrix in KMR, the F-test statistic in GDBR and the score test statistic in KMR are equal (up to some ignorable constants). The result is based on the connections of both methods to linear or logistic (random-effects) regression models.
机译:为了检测与常见和复杂疾病的遗传关联,已经提出了两种功能强大但又完全不同的多标记关联测试:基于基因组距离的回归(GDBR)(Wessel and Schork [2006] Am J Hum Genet 79:821-833)和内核机回归(KMR)(Kwee等人,[2008] Am J Hum Genet 82:386-397; Wu等人,[2010] Am J Hum Genet 86:929-942)。 GDBR基于将一组对象的多标记相似性度量与其特质值的变化相关联,而KMR基于通过核函数或核矩阵对多个标记对性状影响的非参数估计。由于这两种方法既强大又通用,但看起来却大不相同,因此了解它们的具体关系很重要。在此报告中,我们表明,在没有其他协变量的情况下,两种方法在定量或二元特征方面存在惊人的对应关系:如果将相同的正半定矩阵用作中心相似矩阵在GDBR中,作为KMR中的核矩阵,GDBR中的F检验统计量与KMR中的得分检验统计量相等(直到某些可忽略的常数)。结果基于两种方法与线性或逻辑(随机效应)回归模型的联系。

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