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The Maximum-Likelihood-Binomial method revisited: a robust approach for model-free linkage analysis of quantitative traits in large sibships.

机译:重新探讨了最大似然二项式方法:一种用于大型同胞数量特征的无模型关联分析的鲁棒方法。

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摘要

Model-free linkage analysis methods, based on identity-by-descent allele sharing, are commonly used for complex trait analysis. The Maximum-Likelihood-Binomial (MLB) approach, which is based on the hypothesis that parental alleles are binomially distributed among affected sibs, is particularly popular. An extension of this method to quantitative traits (QT) has been proposed (MLB-QTL), based on the introduction of a latent binary variable capturing information about the linkage between the QT and the marker. Interestingly, the MLB-QTL method does not require the decomposition of sibships into constituent sibpairs and requires no prior assumption about the distribution of the QT. We propose a new formulation of the MLB method for quantitative traits (nMLB-QTL) that explicitly takes advantage of the independence of paternal and maternal allele transmission under the null hypothesis of no linkage. Simulation studies under H showed that the nMLB-QTL method generated very consistent type I errors. Furthermore, simulations under the alternative hypothesis showed that the nMLB-QTL method was slightly, but systematically more powerful than the MLB-QTL method, whatever the genetic model, residual correlation, ascertainment strategy and sibship size considered. Finally, the power of the nMLB-QTL method is illustrated by a chromosome-wide linkage scan for a quantitative endophenotype of leprosy infection. Overall, the nMLB-QTL method is a robust, powerful, and flexible approach for detecting linkage with quantitative phenotypes, particularly in studies of non Gaussian phenotypes in large sibships.
机译:基于后裔等位基因共享的无模型连锁分析方法通常用于复杂性状分析。最大似然二项式(MLB)方法特别流行,该方法基于父母等位基因在受影响同胞之间按二项式分布的假设。基于引入潜在的二进制变量来捕获有关QT和标记之间链接的信息,已经提出了将该方法扩展到定量特征(QT)的方法(MLB-QTL)。有趣的是,MLB-QTL方法不需要将同胞分解为组成的同胞对,也不需要事先假设QT的分布。我们提出了针对数量性状(nMLB-QTL)的MLB方法的新公式,该方法明确利用了无关联无效假设下父本和母本等位基因传播的独立性。 H下的仿真研究表明,nMLB-QTL方法产生非常一致的I型错误。此外,在替代假设下的模拟表明,无论考虑遗传模型,残差相关性,确定策略和同胞大小,nMLB-QTL方法都比MLB-QTL方法略强,但系统地更强大。最后,nMLB-QTL方法的功能通过对麻风病感染的定量内表型的全染色体连锁扫描来说明。总体而言,nMLB-QTL方法是一种用于检测与定量表型相关性的鲁棒,强大且灵活的方法,特别是在大型同胞中非高斯表型的研究中。

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