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贝叶斯多数量性状基因座定位中的偏差信息准则(DIC)

Deviance Information Criterion (DIC) in Bayesian Multiple QTL Mapping.

作者信息

Shriner Daniel, Yi Nengjun

机构信息

Department of Biostatistics, Section on Statistical Genetics, University of Alabama at Birmingham, Birmingham, AL 35294.

出版信息

Comput Stat Data Anal. 2009 Mar 15;53(5):1850-1860. doi: 10.1016/j.csda.2008.01.016.

Abstract

Mapping multiple quantitative trait loci (QTL) is commonly viewed as a problem of model selection. Various model selection criteria have been proposed, primarily in the non-Bayesian framework. The deviance information criterion (DIC) is the most popular criterion for Bayesian model selection and model comparison but has not been applied to Bayesian multiple QTL mapping. A derivation of the DIC is presented for multiple interacting QTL models and calculation of the DIC is demonstrated using posterior samples generated by Markov chain Monte Carlo (MCMC) algorithms. The DIC measures posterior predictive error by penalizing the fit of a model (deviance) by its complexity, determined by the effective number of parameters. The effective number of parameters simultaneously accounts for the sample size, the cross design, the number and lengths of chromosomes, covariates, the number of QTL, the type of QTL effects, and QTL effect sizes. The DIC provides a computationally efficient way to perform sensitivity analysis and can be used to quantitatively evaluate if including environmental effects, gene-gene interactions, and/or gene-environment interactions in the prior specification is worth the extra parameterization. The DIC has been implemented in the freely available package R/qtlbim, which greatly facilitates the general usage of Bayesian methodology for genome-wide interacting QTL analysis.

摘要

映射多个数量性状位点(QTL)通常被视为一个模型选择问题。已经提出了各种模型选择标准,主要是在非贝叶斯框架下。偏差信息准则(DIC)是贝叶斯模型选择和模型比较中最流行的准则,但尚未应用于贝叶斯多QTL映射。本文给出了多相互作用QTL模型的DIC推导,并使用马尔可夫链蒙特卡罗(MCMC)算法生成的后验样本演示了DIC的计算。DIC通过根据由有效参数数量决定的模型复杂度对模型拟合(偏差)进行惩罚来衡量后验预测误差。有效参数数量同时考虑了样本大小、交叉设计、染色体数量和长度、协变量、QTL数量、QTL效应类型以及QTL效应大小。DIC提供了一种计算效率高的方法来进行敏感性分析,并且可用于定量评估在先验规范中纳入环境效应、基因-基因相互作用和/或基因-环境相互作用是否值得额外的参数化。DIC已在免费提供的R/qtlbim软件包中实现,这极大地促进了贝叶斯方法在全基因组相互作用QTL分析中的普遍应用。

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