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使用多变量遗传模型检测多效数量性状基因座。

Using multivariate genetic modeling to detect pleiotropic quantitative trait loci.

作者信息

Boomsma D I

机构信息

Department of psychonomics, Vrije Universiteit, Amsterdam, The Netherlands.

出版信息

Behav Genet. 1996 Mar;26(2):161-6. doi: 10.1007/BF02359893.

Abstract

Large numbers of sibling pairs or other relatives are needed to detect linkage between a quantitative trait locus (QTL) and a marker, especially if the variance of the QTL is low relative to the total phenotypic variance of the trait. One strategy to increase the power to detect linkage is to reduce the environmental variance in the trait under analysis. This approach was explored by carrying out a series of simulation studies in which multivariate observations were used to estimate individual genotypic values at a QTL, that pleiotropically affected more than one trait. Simulations for different QTL allele frequencies with a completely informative marker showed that the power to detect the QTL increased substantially when estimates of individual genotypic values at the QTL were used in the linkage analysis instead of phenotypic observations. An advantage of this approach is that, rather than employing phenotypic selection, individuals with extreme genotypes may selected when ascertaining a sample of extreme families.

摘要

需要大量的同胞对或其他亲属来检测数量性状基因座(QTL)与标记之间的连锁关系,特别是当QTL的方差相对于该性状的总表型方差较低时。提高检测连锁能力的一种策略是减少所分析性状的环境方差。通过进行一系列模拟研究来探索这种方法,在这些研究中,使用多变量观测值来估计QTL处的个体基因型值,该QTL多效性地影响多个性状。使用完全信息标记对不同QTL等位基因频率进行的模拟表明,当在连锁分析中使用QTL处个体基因型值的估计值而非表型观测值时,检测QTL的能力会大幅提高。这种方法的一个优点是,在确定极端家系样本时,不是采用表型选择,而是可以选择具有极端基因型的个体。

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