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1.
Mol Biol Evol ; 30(5): 1188-95, 2013 May.
Artigo em Inglês | MEDLINE | ID: mdl-23418397

RESUMO

Nonparametric bootstrap has been a widely used tool in phylogenetic analysis to assess the clade support of phylogenetic trees. However, with the rapidly growing amount of data, this task remains a computational bottleneck. Recently, approximation methods such as the RAxML rapid bootstrap (RBS) and the Shimodaira-Hasegawa-like approximate likelihood ratio test have been introduced to speed up the bootstrap. Here, we suggest an ultrafast bootstrap approximation approach (UFBoot) to compute the support of phylogenetic groups in maximum likelihood (ML) based trees. To achieve this, we combine the resampling estimated log-likelihood method with a simple but effective collection scheme of candidate trees. We also propose a stopping rule that assesses the convergence of branch support values to automatically determine when to stop collecting candidate trees. UFBoot achieves a median speed up of 3.1 (range: 0.66-33.3) to 10.2 (range: 1.32-41.4) compared with RAxML RBS for real DNA and amino acid alignments, respectively. Moreover, our extensive simulations show that UFBoot is robust against moderate model violations and the support values obtained appear to be relatively unbiased compared with the conservative standard bootstrap. This provides a more direct interpretation of the bootstrap support. We offer an efficient and easy-to-use software (available at http://www.cibiv.at/software/iqtree) to perform the UFBoot analysis with ML tree inference.


Assuntos
Funções Verossimilhança , Simulação por Computador , Filogenia
2.
Mol Biol Evol ; 28(1): 143-52, 2011 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-20643866

RESUMO

As models of sequence evolution become more and more complicated, many criteria for model selection have been proposed, and tools are available to select the best model for an alignment under a particular criterion. However, in many instances the selected model fails to explain the data adequately as reflected by large deviations between observed pattern frequencies and the corresponding expectation. We present MISFITS, an approach to evaluate the goodness of fit (http://www.cibiv.at/software/misfits). MISFITS introduces a minimum number of "extra substitutions" on the inferred tree to provide a biologically motivated explanation why the alignment may deviate from expectation. These extra substitutions plus the evolutionary model then fully explain the alignment. We illustrate the method on several examples and then give a survey about the goodness of fit of the selected models to the alignments in the PANDIT database.


Assuntos
Algoritmos , Modelos Genéticos , Alinhamento de Sequência/métodos , Análise de Sequência de Proteína/métodos , Software , Animais , Sequência de Bases , DNA Mitocondrial/análise , DNA Mitocondrial/genética , Bases de Dados Genéticas , Evolução Molecular , Humanos , Funções Verossimilhança , Dados de Sequência Molecular , Filogenia , Primatas/genética , Homologia de Sequência do Ácido Nucleico
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