arXivDaily arXiv每日学术速递 周一至周五更新
arXiv 1611.03361q-bio.QMstat.ME
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通过高斯浓度图模型模拟全基因组预测中的相关标记效应

Modelling correlated marker effects in genome-wide prediction via Gaussian concentration graph models

Carlos Alberto Martínez, Kshitij Khare, Syed Rahman, Mauricio A. Elzo

摘要:

在全基因组预测中,通常假设标记等位基因置换效应独立;然而,自该技术的早期阶段以来,已知自然指向相关效应。在统计学中,图形模型已被确定为一个有用的和强大的工具,在高维问题的协方差估计,它是一个领域,最近经历了一个很大的扩张。特别是高斯浓度图模型(GCGM)已被广泛研究。在这些模型中,一组随机变量的分布,在这种情况下是标记效应,被假设为关于无向图G的马尔可夫。本文发展了贝叶斯(BayesG和BayesG-D)和频率论(GML-BLUP)方法,将GCGM理论应用于全基因组预测。提出了基于领域知识的图G的不同定义方法,证明了两个命题和一个推论,建立了可分解图的判定条件。这些方法在小型模拟和真实数据集上实现。在我们的模拟中,考虑了等位基因取代效应之间的相关性预计会由于各种原因而出现的情况,并根据物理标记位置定义了图表。结果表明,改善表型和预测育种值和预测育种值的准确性之间的相关性时,占部分相关的等位基因取代的影响。扩展多等位基因位点的情况下进行了描述,并讨论了一些可能的改进,将更灵活的先验贝叶斯设置。我们的模型是有前途的,因为它们允许在预测过程中纳入生物信息,因为它们比以前提出的相关标记效应的其他模型更灵活和通用。

英文摘要:

In genome-wide prediction, independence of marker allele substitution effects is typically assumed; however, since early stages of this technology it has been known that nature points to correlated effects. In statistics, graphical models have been identified as a useful and powerful tool for covariance estimation in high dimensional problems and it is an area that has recently experienced a great expansion. In particular, Gaussian concentration graph models (GCGM) have been widely studied. These are models in which the distribution of a set of random variables, the marker effects in this case, is assumed to be Markov with respect to an undirected graph G. In this paper, Bayesian (Bayes G and Bayes G-D) and frequentist (GML-BLUP) methods adapting the theory of GCGM to genome-wide prediction were developed. Different approaches to define the graph G based on domain-specific knowledge were proposed, and two propositions and a corollary establishing conditions to find decomposable graphs were proven. These methods were implemented in small simulated and real datasets. In our simulations, scenarios where correlations among allelic substitution effects were expected to arise due to various causes were considered, and graphs were defined on the basis of physical marker positions. Results showed improvements in correlation between phenotypes and predicted breeding values and accuracies of predicted breeding values when accounting for partially correlated allele substitution effects. Extensions to the multiallelic loci case were described and some possible refinements incorporating more flexible priors in the Bayesian setting were discussed. Our models are promising because they allow incorporation of biological information in the prediction process, and because they are more flexible and general than other models accounting for correlated marker effects that have been proposed previously.

机构、总结、中文摘要均由AI分析而来,可能存在错误,请以论文正文为准。

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