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Covariance Association Test (CVAT) Identifies Genetic Markers Associated with Schizophrenia in Functionally Associated Biological Processes

机译:协方差关联测试(CVAT)识别功能相关的生物学过程中与精神分裂症相关的遗传标记

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摘要

Schizophrenia is a psychiatric disorder with large personal and social costs, and understanding the genetic etiology is important. Such knowledge can be obtained by testing the association between a disease phenotype and individual genetic markers; however, such single-marker methods have limited power to detect genetic markers with small effects. Instead, aggregating genetic markers based on biological information might increase the power to identify sets of genetic markers of etiological significance. Several set test methods have been proposed: Here we propose a new set test derived from genomic best linear unbiased prediction (GBLUP), the covariance association test (CVAT). We compared the performance of CVAT to other commonly used set tests. The comparison was conducted using a simulated study population having the same genetic parameters as for schizophrenia. We found that CVAT was among the top performers. When extending CVAT to utilize a mixture of SNP effects, we found an increase in power to detect the causal sets. Applying the methods to a Danish schizophrenia case–control data set, we found genomic evidence for association of schizophrenia with vitamin A metabolism and immunological responses, which previously have been implicated with schizophrenia based on experimental and observational studies.
机译:精神分裂症是一种精神疾病,需要付出大量个人和社会代价,因此了解遗传病因很重要。可以通过测试疾病表型与单个遗传标记之间的关联来获得这些知识。但是,这种单标记方法检测基因标记的能力有限,影响很小。取而代之的是,基于生物学信息聚合遗传标记可能会提高识别具有病因意义的遗传标记集的能力。已经提出了几种集合检验方法:在这里,我们提出了一个新的集合检验,它是从基因组最佳线性无偏预测(GBLUP)中得出的,即协方差关联检验(CVAT)。我们将CVAT的性能与其他常用设置测试进行了比较。使用具有与精神分裂症相同的遗传参数的模拟研究人群进行比较。我们发现CVAT是表现最好的公司之一。当扩展CVAT以利用SNP效果的混合时,我们发现检测因果关系的能力增加了。将这些方法应用于丹麦精神分裂症的病例对照数据集,我们发现了与精神分裂症与维生素A代谢和免疫反应相关的基因组证据,以前基于实验和观察研究,这些证据与精神分裂症有关。

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