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Quantification and relative severity of inflated branch-support values generated by alternative methods: An empirical example

机译:替代方法生成的膨胀支支值的量化和相对严重性:一个经验示例

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A supermatrix of 272 terminals from Rubiaceae tribe Spermacoceae that were scored for up to 10 gene regions (two nrDNA, eight plastid) was used as an empirical example to quantify sources of error in heuristic parametric (Bayesian MCMC and maximum likelihood) phylogenetic analyses. The supermatrix includes dramatic disparities in which terminals were sampled for which gene regions. The sources of error examined include poor quality tree searches, requiring a single fully resolved optimal tree, undersampling-within-replicates and frequency-within-replicates bootstrap artifacts, and extrapolation from one character partition to another such that synapomorphies that would only be ambiguously optimized by parsimony are optimized with high probability by parametric methods. Four of our conclusions are as follows. (1) The resolution and support provided by parametric methods for clades that lack unambiguously optimized (by parsimony) synapomorphies are less robust to the addition of terminals and characters than those clades that have unambiguously optimized synapomorphies. (2) Those tree-search methods which can create phylogenetic artifacts (frequency-within-replicates resampling, undersampling-within-replicates resampling, requiring a single fully resolved optimal tree, non-independent resampling among replicates) provide the greatest resolution and support irrespective of whether that resolution or support is corroborated by more conservative and better justified methods. (3) Partitioning data matrices cannot be relied upon to consistently obviate potentially dubious resolution and support caused by missing-data artifacts in likelihood analyses when the models require linked branch lengths among partitions. (4) Undersampling-within-replicates and frequency-within-replicates resampling artifacts are not unique to parsimony and should be accounted for in likelihood analyses by allowing multiple equally likely trees to be saved within each resampling pseudoreplicate and applying the strict-consensus bootstrap rather than the frequency-within-replicates bootstrap.
机译:以茜草科的272个末端的超级矩阵为基础,对10个基因区域(两个nrDNA,八个质体)进行了评分,以此作为经验示例来量化启发式参数(贝叶斯MCMC和最大似然)系统发育分析中的错误来源。超级矩阵包括显着的差异,其中对哪个基因区域进行了末端采样。检查的错误源包括质量较差的树搜索,需要单个完全解析的最佳树,重复采样不足和重复频率自举伪像,以及从一个字符分区外推到另一个字符分区,以使得只能对歧义进行优化的歧义通过参数方法高概率地优化了简约性。我们的四个结论如下。 (1)参数方法为没有明确优化(通过简约性)同形同义的进化枝所提供的分辨率和支持,比那些具有明确优化的同形同义的进化枝,对增加终端和字符的鲁棒性更差。 (2)可以创建系统发生伪像的树搜索方法(重复内重复采样频率,重复内欠采样采样,需要单个完全解析的最佳树,重复之间非独立重新采样)提供了最大的分辨率和支持该决议或支持是否被更保守,更合理的方法所证实。 (3)当模型需要分区之间的链接分支长度时,不能依赖分区数据矩阵来始终消除潜在性可疑解决方案和可能性分析中缺失数据伪像所引起的不确定性。 (4)复制内欠采样和复制内重复频率伪影不是简约性独有的,应该通过允许在每个重新采样伪复制中保存多个相同可能性的树并应用严格共识的引导程序来在可能性分析中解决。而不是复制内引导的频率。

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