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Searching for Recursive Causal Structures in Multivariate Quantitative Genetics Mixed Models

机译:在多元定量遗传混合模型中寻找递归因果结构

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摘要

Biology is characterized by complex interactions between phenotypes, such as recursive and simultaneous relationships between substrates and enzymes in biochemical systems. Structural equation models (SEMs) can be used to study such relationships in multivariate analyses, e.g., with multiple traits in a quantitative genetics context. Nonetheless, the number of different recursive causal structures that can be used for fitting a SEM to multivariate data can be huge, even when only a few traits are considered. In recent applications of SEMs in mixed-model quantitative genetics settings, causal structures were preselected on the basis of prior biological knowledge alone. Therefore, the wide range of possible causal structures has not been properly explored. Alternatively, causal structure spaces can be explored using algorithms that, using data-driven evidence, can search for structures that are compatible with the joint distribution of the variables under study. However, the search cannot be performed directly on the joint distribution of the phenotypes as it is possibly confounded by genetic covariance among traits. In this article we propose to search for recursive causal structures among phenotypes using the inductive causation (IC) algorithm after adjusting the data for genetic effects. A standard multiple-trait model is fitted using Bayesian methods to obtain a posterior covariance matrix of phenotypes conditional to unobservable additive genetic effects, which is then used as input for the IC algorithm. As an illustrative example, the proposed methodology was applied to simulated data related to multiple traits measured on a set of inbred lines.
机译:生物学的特征是表型之间复杂的相互作用,例如生化系统中底物和酶之间的递归和同时关系。结构方程模型(SEM)可用于在多变量分析中研究此类关系,例如,在定量遗传学背景下具有多个特征。但是,即使只考虑了几个特征,可用于将SEM拟合到多元数据的不同递归因果结构的数量也可能很大。在混合模型定量遗传学设置中的SEM的最新应用中,仅基于先验生物学知识预先选择了因果结构。因此,尚未广泛探讨各种可能的因果结构。或者,可以使用算法探索因果结构空间,这些算法使用数据驱动的证据,可以搜索与所研究变量的联合分布兼容的结构。但是,不能直接对表型的联合分布进行搜索,因为它可能与性状之间的遗传协方差混淆。在本文中,我们建议在调整遗传效应数据后,使用归因因果(IC)算法在表型之间搜索递归因果结构。使用贝叶斯方法拟合标准的多特征模型,以获得表型的后协方差矩阵,其条件是不可观测的累加遗传效应,然后将其用作IC算法的输入。作为说明性例子,将所提出的方法应用于与在一组自交系上测量的多个性状有关的模拟数据。

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