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首页> 外文期刊>Genetic epidemiology. >CAPL: a novel association test using case-control and family data and accounting for population stratification.
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CAPL: a novel association test using case-control and family data and accounting for population stratification.

机译:CAPL:一种新颖的关联测试,使用病例对照和家庭数据并考虑了人口分层。

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The recent successes of GWAS based on large sample sizes motivate combining independent datasets to obtain larger sample sizes and thereby increase statistical power. Analysis methods that can accommodate different study designs, such as family-based and case-control designs, are of general interest. However, population stratification can cause spurious association for population-based association analyses. For family-based association analysis that infers missing parental genotypes based on the allele frequencies estimated in the entire sample, the parental mating-type probabilities may not be correctly estimated in the presence of population stratification. Therefore, any approach to combining family and case-control data should also properly account for population stratification. Although several methods have been proposed to accommodate family-based and case-control data, all have restrictions. Most of them require sampling a homogeneous population, which may not be a reasonable assumption for data from a large consortium. One of the methods, FamCC, can account for population stratification and uses nuclear families with arbitrary number of siblings but requires parental genotype data, which are often unavailable for late-onset diseases. We extended the family-based test, Association in the Presence of Linkage (APL), to combine family and case-control data (CAPL). CAPL can accommodate case-control data and families with multiple affected siblings and missing parents in the presence of population stratification. We used simulations to demonstrate that CAPL is a valid test either in a homogeneous population or in the presence of population stratification. We also showed that CAPL can have more power than other methods that combine family and case-control data.
机译:基于大样本量的GWAS的最新成功促使将独立的数据集结合起来以获得更大的样本量,从而提高了统计能力。能够适应不同研究设计的分析方法,例如基于家庭的设计和病例对照设计,是人们普遍关注的问题。但是,人口分层可能导致基于人口的关联分析的虚假关联。对于基于整个样本中估计的等位基因频率推断缺失的父母基因型的基于家庭的关联分析,在存在群体分层的情况下,可能无法正确估计父母的交配类型概率。因此,将家庭和病例对照数据相结合的任何方法也应适当考虑人口分层。尽管已经提出了几种方法来容纳基于家庭和病例对照的数据,但是所有方法都有局限性。它们中的大多数都需要对同质种群进行采样,对于来自大型财团的数据而言,这可能不是一个合理的假设。一种方法是FamCC,它可以解决人口分层问题,并使用具有任意数量同胞的核心家庭,但需要父母基因型数据,而这些数据通常对于晚期发病是不可用的。我们扩展了基于家庭的测试,即“存在链接中的关联”(APL),以结合家庭和病例对照数据(CAPL)。在人口分层的情况下,CAPL可以容纳病例对照数据和有多个受影响兄弟姐妹且父母失踪的家庭。我们使用模拟来证明CAPL在同质人口或存在人口分层的情况下都是有效的测试。我们还表明,CAPL比结合家庭和病例对照数据的其他方法具有更大的功能。

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