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动态性状数量性状位点的贝叶斯收缩分析

Bayesian shrinkage analysis of quantitative trait Loci for dynamic traits.

作者信息

Yang Runqing, Xu Shizhong

机构信息

School of Agriculture and Biology, Shanghai Jiaotong University, Shanghai 201101, People's Republic of China.

出版信息

Genetics. 2007 Jun;176(2):1169-85. doi: 10.1534/genetics.106.064279. Epub 2007 Apr 15.

Abstract

Many quantitative traits are measured repeatedly during the life of an organism. Such traits are called dynamic traits. The pattern of the changes of a dynamic trait is called the growth trajectory. Studying the growth trajectory may enhance our understanding of the genetic architecture of the growth trajectory. Recently, we developed an interval-mapping procedure to map QTL for dynamic traits under the maximum-likelihood framework. We fit the growth trajectory by Legendre polynomials. The method intended to map one QTL at a time and the entire QTL analysis involved scanning the entire genome by fitting multiple single-QTL models. In this study, we propose a Bayesian shrinkage analysis for estimating and mapping multiple QTL in a single model. The method is a combination between the shrinkage mapping for individual quantitative traits and the Legendre polynomial analysis for dynamic traits. The multiple-QTL model is implemented in two ways: (1) a fixed-interval approach where a QTL is placed in each marker interval and (2) a moving-interval approach where the position of a QTL can be searched in a range that covers many marker intervals. Simulation study shows that the Bayesian shrinkage method generates much better signals for QTL than the interval-mapping approach. We propose several alternative methods to present the results of the Bayesian shrinkage analysis. In particular, we found that the Wald test-statistic profile can serve as a mechanism to test the significance of a putative QTL.

摘要

许多数量性状在生物体的生命过程中会被反复测量。这类性状被称为动态性状。动态性状的变化模式被称为生长轨迹。研究生长轨迹可能会增进我们对生长轨迹遗传结构的理解。最近,我们开发了一种区间作图程序,用于在最大似然框架下对动态性状的数量性状基因座(QTL)进行定位。我们用勒让德多项式拟合生长轨迹。该方法旨在一次定位一个QTL,整个QTL分析涉及通过拟合多个单QTL模型来扫描整个基因组。在本研究中,我们提出一种贝叶斯收缩分析方法,用于在单个模型中估计和定位多个QTL。该方法是个体数量性状的收缩定位与动态性状的勒让德多项式分析的结合。多QTL模型通过两种方式实现:(1)固定区间方法,即在每个标记区间放置一个QTL;(2)移动区间方法,即在覆盖多个标记区间的范围内搜索QTL的位置。模拟研究表明,贝叶斯收缩方法比区间作图方法能产生更好的QTL信号。我们提出了几种替代方法来呈现贝叶斯收缩分析的结果。特别是,我们发现Wald检验统计量分布图可作为检验假定QTL显著性的一种机制。

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