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Mapping quantitative trait loci in the case of a spike in the phenotype distribution.在表型分布出现峰值的情况下定位数量性状基因座。
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具有性状分布峰值的数量性状基因座的多区间定位

Multiple-interval mapping for quantitative trait loci with a spike in the trait distribution.

作者信息

Li Wenyun, Chen Zehua

机构信息

School of Mathematics and Computational Science, Sun Yat-Sen University, Guangzhou, People's Republic of China.

出版信息

Genetics. 2009 May;182(1):337-42. doi: 10.1534/genetics.108.099028. Epub 2009 Mar 2.

DOI:10.1534/genetics.108.099028
PMID:19258307
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2674830/
Abstract

For phenotypic distributions where many individuals share a common value-such as survival time following a pathogenic infection-a spike occurs at that common value. This spike affects quantitative trait loci (QTL) mapping methodologies and causes standard approaches to perform suboptimally. In this article, we develop a multiple-interval mapping (MIM) procedure based on mixture generalized linear models (GLIMs). An extended Bayesian information criterion (EBIC) is used for model selection. To demonstrate its utility, this new approach is compared to single-QTL models that appropriately handle the phenotypic distribution. The method is applied to data from Listeria infection as well as data from simulation studies. Compared to the single-QTL model, the findings demonstrate that the MIM procedure greatly improves the efficiency in terms of positive selection rate and false discovery rate. The method developed has been implemented using functions in R and is freely available to download and use.

摘要

对于许多个体具有共同值的表型分布,例如致病性感染后的存活时间,在该共同值处会出现一个峰值。这个峰值会影响数量性状基因座(QTL)定位方法,并导致标准方法的性能次优。在本文中,我们基于混合广义线性模型(GLIM)开发了一种多区间定位(MIM)程序。使用扩展贝叶斯信息准则(EBIC)进行模型选择。为了证明其效用,将这种新方法与适当处理表型分布的单QTL模型进行了比较。该方法应用于来自李斯特菌感染的数据以及模拟研究的数据。与单QTL模型相比,研究结果表明,MIM程序在阳性选择率和错误发现率方面大大提高了效率。所开发的方法已使用R语言中的函数实现,可免费下载和使用。