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Likelihood-based clustering (LiBaC) for codon models, a method for grouping sites according to similarities in the underlying process of evolution

机译:用于密码子模型的基于可能性的聚类(LiBaC),一种根据潜在进化过程中的相似性对位点进行分组的方法

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摘要

Models of codon evolution are useful for investigating the strength and direction of natural selection via a parameter for the nonsynonymous/synonymous rate ratio (omega = d(N)/d(S)). Different codon models are available to account for diversity of the evolutionary patterns among sites. Codon models that specify data partitions as fixed effects allow the most evolutionary diversity among sites but require that site partitions are a priori identifiable. Models that use a parametric distribution to express the variability in the omega ratio across site do not require a priori partitioning of sites, but they permit less among-site diversity in the evolutionary process. Simulation studies presented in this paper indicate that differences among sites in estimates of omega under an overly simplistic analytical model can reflect more than just natural selection pressure. We also find that the classic likelihood ratio tests for positive selection have a high false-positive rate in some situations. In this paper, we developed a new method for assigning codon sites into groups where each group has a different model, and the likelihood over all sites is maximized. The method, called likelihood-based clustering (LiBaC), can be viewed as a generalization of the family of model-based clustering approaches to models of codon evolution. We report the performance of several LiBaC-based methods, and selected alternative methods, over a wide variety of scenarios. We find that LiBaC, under an appropriate model, can provide reliable parameter estimates when the process of evolution is very heterogeneous among groups of sites. Certain types of proteins, such as transmembrane proteins, are expected to exhibit such heterogeneity. A survey of genes encoding transmembrane proteins suggests that overly simplistic models could be leading to false signal for positive selection among such genes. In these cases, LiBaC-based methods offer an important addition to a "toolbox" of methods thereby helping to uncover robust evidence for the action of positive selection.
机译:密码子进化模型可用于通过非同义/同义比率(omega = d(N)/ d(S))的参数研究自然选择的强度和方向。可使用不同的密码子模型来解释位点之间进化模式的多样性。将数据分区指定为固定效果的密码子模型允许站点之间具有最大的进化多样性,但要求站点分区是先验可识别的。使用参数分布来表示整个站点中欧米伽比的可变性的模型不需要对站点进行先验划分,但是它们在进化过程中允许较少的站点间多样性。本文介绍的模拟研究表明,在过于简单的分析模型下,欧米茄估计值的位点之间的差异不仅可以反映自然选择压力。我们还发现,在某些情况下,用于正选择的经典似然比检验具有较高的假阳性率。在本文中,我们开发了一种将密码子位点分配到组的新方法,其中每个组具有不同的模型,并且所有位点的可能性均最大化。该方法称为基于似然的聚类(LiBaC),可以看作是密码子进化模型的基于模型的聚类方法系列的概括。我们报告了在多种情况下几种基于LiBaC的方法和选择的替代方法的性能。我们发现,在适当的模型下,当进化过程在站点组之间非常异质时,LiBaC可以提供可靠的参数估计。某些类型的蛋白质,例如跨膜蛋白质,有望表现出这种异质性。对编码跨膜蛋白的基因进行的一项调查表明,过于简单的模型可能会导致在此类基因中进行阳性选择的错误信号。在这些情况下,基于LiBaC的方法为方法的“工具箱”提供了重要的补充,从而有助于为正选择的作用找到可靠的证据。

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