Lee Chaeyoung, Kim Younyoung
Department of Bioinformatics and Life Science, Soongsil University, Seoul,156-743, Korea.
Genomics. 2008 Dec;92(6):446-51. doi: 10.1016/j.ygeno.2008.08.006. Epub 2008 Oct 1.
A simulation study was conducted to provide a practical guideline for experimental designs with the Bayesian approach using Gibbs sampling (BAGS), a recently developed method for estimating interaction among multiple loci. Various data sets were simulated from combinations of number of loci, within-genotype variance, sample size, and balance of design. Mean square prediction error (MSPE) and empirical statistical power were obtained from estimating and testing the posterior mean estimate of combination genotypic effect. Simultaneous use of both MSPE and power was suggested to find an optimal design because their correlation estimate (-0.8) would not be large enough to ignore either of them. The optimal sample sizes with MSPE >2.0 and power >0.8 with the within-genotype variance of 30 were 135, 675, and >8100 for 2-, 3-, and 4-locus unbalanced data. The BAGS was suggested for interaction effects among limited number (4 or less) of loci in practice. A practical guideline for determining an optimal sample size with a given power or vise versa is provided for BAGS.
开展了一项模拟研究,旨在为采用吉布斯采样的贝叶斯方法(BAGS)进行实验设计提供实用指南,BAGS是一种最近开发的用于估计多个基因座间相互作用的方法。从基因座数量、基因型内方差、样本量和设计平衡的组合中模拟了各种数据集。通过估计和检验组合基因型效应的后验均值估计值,获得了均方预测误差(MSPE)和经验统计功效。建议同时使用MSPE和功效来找到最优设计,因为它们的相关估计值(-0.8)不够大,不能忽略其中任何一个。对于基因型内方差为30的2个、3个和4个基因座的不平衡数据,MSPE>2.0且功效>0.8时的最优样本量分别为135、675和>8100。在实际应用中,对于有限数量(4个或更少)基因座间的相互作用效应,建议使用BAGS。为BAGS提供了在给定功效下确定最优样本量或反之亦然的实用指南。