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Bayesian selection of continuous-time Markov chain evolutionary models

机译:连续时间马尔可夫链演化模型的贝叶斯选择

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摘要

We develop a reversible jump Markov chain Monte Carlo approach to estimating the posterior distribution of phylogenies based on aligned DNA/RNA sequences under several hierarchical evolutionary models. Using a proper, yet nontruncated and uninformative prior., we demonstrate the advantages of the Bayesian approach to hypothesis testing and estimation in phylogenetics by comparing different models for the infinitesimal rates of change among nucleotides, for the number of rate classes, and for the relationships among branch lengths. We compare the relative probabilities of these models and the appropriateness of a molecular clock using Bayes factors. Our most general model, first proposed by Tamura and Nei, parameterizes the infinitesimal change probabilities among nucleotides (A, G, C, T/U) into six parameters, consisting of three parameters for the nucleotide stationary distribution, two rate parameters for nucleotide transitions, and another parameter for nucleotide transversions. Nested models include the Hasegawa, Kishino, and Yano model with equal transition sates and the Kimura model with a uniform stationary distribution and equal transition rates. To illustrate our methods, we examine simulated data, 16S rRNA sequences from 15 contemporary eubacteria, halobacteria, eocytes, and eukaryotes, 9 primates, and the entire HIV genome of 11 isolates. We find that the Kimura model is too restrictive, that the Hasegawa, Kishino, and Yano model can be rejected for some data sets, that there is evidence for more than one rate class and a molecular clock among similar taxa, and that a molecular clock can be rejected for more distantly related taxa.
机译:我们开发了一种可逆跳跃马尔可夫链蒙特卡罗方法,在几个分层进化模型下基于对齐的 DNA/RNA 序列来估计系统发育的后验分布。使用适当的,但未截断且无信息的先验,我们通过比较核苷酸之间无穷小变化率的不同模型,速率类别的数量以及分支长度之间的关系,证明了贝叶斯方法在系统发育学中假设检验和估计的优势。我们比较了这些模型的相对概率和使用贝叶斯因子的分子钟的适当性。我们最通用的模型,首先由Tamura和Nei提出,将核苷酸(A、G、C、T/U)之间的无穷小变化概率参数化为六个参数,包括三个核苷酸平稳分布参数、两个核苷酸转化速率参数和另一个核苷酸转位参数。嵌套模型包括具有相等过渡态的长谷川、岸野和矢野模型,以及具有均匀平稳分布和相等跃迁速率的木村模型。为了说明我们的方法,我们检查了模拟数据,来自15种当代真细菌,盐细菌,卵母细胞和真核生物的16S rRNA序列,9种灵长类动物以及11种分离株的整个HIV基因组。我们发现木村模型的限制性太强,长谷川、岸野和矢野模型可以被某些数据集拒绝,有证据表明相似的分类群中存在不止一个速率类和分子钟,而分子钟可以被拒绝用于更远的相关分类群。

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