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首页> 外文期刊>Genetics, selection, evolution >Improving the computational efficiency of fully Bayes inference and assessing the effect of misspecification of hyperparameters in whole-genome prediction models
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Improving the computational efficiency of fully Bayes inference and assessing the effect of misspecification of hyperparameters in whole-genome prediction models

机译:提高全贝叶斯推理的计算效率,并评估全基因组预测模型中超参数的错误指定的影响

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Background The reliability of whole-genome prediction models (WGP) based on using high-density single nucleotide polymorphism (SNP) panels critically depends on proper specification of key hyperparameters. A currently popular WGP model labeled BayesB specifies a hyperparameter π, that is `loosely used to describe the proportion of SNPs that are in linkage disequilibrium (LD) with causal variants. The remaining markers are specified to be random draws from a Student t distribution with key hyperparameters being degrees of freedom v and scale s2. Methods We consider three alternative Markov chain Monte Carlo (MCMC) approaches based on the use of Metropolis-Hastings (MH) to estimate these key hyperparameters. The first approach, termed DFMH, is based on a previously published strategy for which s2 is drawn by a Gibbs step and v is drawn by a MH step. The second strategy, termed UNIMH, substitutes MH for Gibbs when drawing s2 and further collapses or marginalizes the full conditional density of v. The third strategy, termed BIVMH, is based on jointly drawing the two hyperparameters in a bivariate MH step. We also tested the effect of misspecification of s2 for its effect on accuracy of genomic estimated breeding values (GEBV), yet allowing for inference on the other hyperparameters. Results The UNIMH and BIVMH strategies had significantly greater (P?v and s2 than DFMH in BayesA (π?=?1) and BayesB implementations. We drew similar conclusions based on an analysis of the public domain heterogeneous stock mice data. We also determined significant drops (P?s2, whereas BayesB was more robust to such misspecifications. However, understating s2 was compensated by counterbalancing inferences on v in BayesA and BayesB, and on π in BayesB. Conclusions Sampling strategies based solely on MH updates of v and s2, and collapsed representations of full conditional densities can improve the computational efficiency of MCMC relative to the use of Gibbs updates. We believe that proper inferences on s2, v and π are vital to ensure that the accuracy of GEBV is maximized when using parametric WGP models.
机译:背景技术基于使用高密度单核苷酸多态性(SNP)面板的全基因组预测模型(WGP)的可靠性关键取决于关键超参数的正确规范。当前流行的标记为BayesB的WGP模型指定了一个超参数π,它“宽松地用于描述因果变异导致连锁不平衡(LD)的SNP的比例。其余标记被指定为来自Student t分布的随机绘图,关键超参数为自由度v和比例s 2 。方法我们考虑使用Metropolis-Hastings(MH)来估计这些关键超参数的三种备选马尔可夫链蒙特卡洛(MCMC)方法。第一种方法称为DFMH,是基于先前发布的策略,通过gibbs步骤绘制s 2 ,通过MH步骤绘制v。第二种策略称为UNIMH,在绘制s 2 时用MH代替Gibbs,并进一步折叠或边缘化v的全部条件密度。第三种策略称为BIVMH,是基于共同绘制两个超参数双变量MH步骤。我们还测试了s 2 的错误指定对基因组估计育种值(GEBV)准确性的影响,但可以推断其他超参数。结果在BayesA(π?=?1)和BayesB实施中,UNIMH和BIVMH策略具有比DFMH显着更大的(P?v和s 2 ),基于对公共领域的分析,我们得出了类似的结论。我们还确定了显着的下降(P?s 2 ,而BayesB对于这种错误指定更为可靠。但是,通过平衡对以下信息的推断,低估了s 2 可以得到补偿:结论完全基于v和s 2 的MH更新以及完全条件密度的折叠表示的采样策略可以提高MCMC相对于MMC的计算效率。我们相信使用s 2 ,v和π进行正确的推论对于确保使用参数WGP模型最大化GEBV的准确性至关重要。

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