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Variance components genetic association test for zero-inflated count outcomes

机译:variance组分归零计数结果的遗传结合试验

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Commonly in biomedical research, studies collect data in which an outcome measure contains informative excess zeros; for example, when observing the burden of neuritic plaques (NPs) in brain pathology studies, those who show none contribute to our understanding of neurodegenerative disease. The outcome may be characterized by a mixture distribution with one component being the "structural zero" and the other component being a Poisson distribution. We propose a novel variance components score test of genetic association between a set of genetic markers and a zero-inflated count outcome from a mixture distribution. This test shares advantageous properties with single-nucleotide polymorphism (SNP)-set tests which have been previously devised for standard continuous or binary outcomes, such as the sequence kernel association test. In particular, our method has superior statistical power compared to competing methods, especially when there is correlation within the group of markers, and when the SNPs are associated with both the mixing proportion and the rate of the Poisson distribution. We apply the method to Alzheimer's data from the Rush University Religious Orders Study and Memory and Aging Project, where as proof of principle we find highly significant associations with the APOE gene, in both the "structural zero" and "count" parameters, when applied to a zero-inflated NPs count outcome.
机译:通常在生物医学研究中,研究收集结果措施的数据含有信息量过多的零;例如,当观察大脑病理研究中神经斑块(NPS)的负担时,表现出没有促进我们对神经变性疾病的理解的人。结果可以通过混合分布分布,其中一个组分是“结构零”,另一个部件是泊松分布。我们提出了一组遗传标记与混合物分布的一组遗传标记和零充气计数结果之间的遗传关联的新颖性方差分量试验。该测试与先前已经设计用于标准连续或二进制结果的单核苷酸多态性(SNP)-SET试验的有利性质分享有利的性质,例如序列核结合试验。特别是,与竞争方法相比,我们的方法具有卓越的统计功率,特别是当在标记组内存在相关性时,并且当SNP与混合比例和泊松分布的速率相关时。我们将该方法应用于Alzheimer的数据来自Rush大学宗教订单学习和记忆和老化项目,作为原则的证据,我们在施加时,我们发现与APOE基因的高度重要关联。零充气的NPS计数结果。

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