ArticleBMC evolutionary biology2015
Automatic selection of partitioning schemes for phylogenetic analyses using iterative k-means clustering of site rates.
Article in BMC evolutionary biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.
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37 citing papers in PubMed.
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- Assessing the suitability of mitochondrial and nuclear DNA genetic markers for molecular systematics and species identification of helminths.Parasites & vectors · 2021Article
- Three new species ofMycoKeys · 2021Review
- Mirage: estimation of ancestral gene-copy numbers by considering different evolutionary patterns among gene families.Bioinformatics advances · 2021Article
- mPartition: A Model-Based Method for Partitioning Alignments.Journal of molecular evolution · 2020Article
- An integrative phylogenomic approach to elucidate the evolutionary history and divergence times of Neuropterida (Insecta: Holometabola).BMC evolutionary biology · 2020Article
- Evolutionary history of Polyneoptera and its implications for our understanding of early winged insects.Proceedings of the National Academy of Sciences of the United States of America · 2019Article
- Current Affairs of Microbial Genome-Wide Association Studies: Approaches, Bottlenecks and Analytical Pitfalls.Frontiers in microbiology · 2019Review
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4 authors.
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No grant is acknowledged in the PubMed record.
Abstract
backgroundModel selection is a vital part of most phylogenetic analyses, and accounting for the heterogeneity in evolutionary patterns across sites is particularly important. Mixture models and partitioning are commonly used to account for this variation, and partitioning is the most popular approach. Most current partitioning methods require some a priori partitioning scheme to be defined, typically guided by known structural features of the sequences, such as gene boundaries or codon positions. Recent evidence suggests that these a priori boundaries often fail to adequately account for variation in rates and patterns of evolution among sites. Furthermore, new phylogenomic datasets such as those assembled from ultra-conserved elements lack obvious structural features on which to define a priori partitioning schemes. The upshot is that, for many phylogenetic datasets, partitioned models of molecular evolution may be inadequate, thus limiting the accuracy of downstream phylogenetic analyses.
resultsWe present a new algorithm that automatically selects a partitioning scheme via the iterative division of the alignment into subsets of similar sites based on their rates of evolution. We compare this method to existing approaches using a wide range of empirical datasets, and show that it consistently leads to large increases in the fit of partitioned models of molecular evolution when measured using AICc and BIC scores. In doing so, we demonstrate that some related approaches to solving this problem may have been associated with a small but important bias.
conclusionsOur method provides an alternative to traditional approaches to partitioning, such as dividing alignments by gene and codon position. Because our method is data-driven, it can be used to estimate partitioned models for all types of alignments, including those that are not amenable to traditional approaches to partitioning.
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