Maximum likelihood phylogenetic estimation from DNA sequences with variable rates over sites: approximate methods

J Mol Evol. 1994 Sep;39(3):306-14. doi: 10.1007/BF00160154.

Abstract

Two approximate methods are proposed for maximum likelihood phylogenetic estimation, which allow variable rates of substitution across nucleotide sites. Three data sets with quite different characteristics were analyzed to examine empirically the performance of these methods. The first, called the "discrete gamma model," uses several categories of rates to approximate the gamma distribution, with equal probability for each category. The mean of each category is used to represent all the rates falling in the category. The performance of this method is found to be quite good, and four such categories appear to be sufficient to produce both an optimum, or near-optimum fit by the model to the data, and also an acceptable approximation to the continuous distribution. The second method, called "fixed-rates model", classifies sites into several classes according to their rates predicted assuming the star tree. Sites in different classes are then assumed to be evolving at these fixed rates when other tree topologies are evaluated. Analyses of the data sets suggest that this method can produce reasonable results, but it seems to share some properties of a least-squares pairwise comparison; for example, interior branch lengths in nonbest trees are often found to be zero. The computational requirements of the two methods are comparable to that of Felsenstein's (1981, J Mol Evol 17:368-376) model, which assumes a single rate for all the sites.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • DNA, Mitochondrial / genetics
  • Genetic Variation / genetics*
  • Globins / genetics
  • Humans
  • Likelihood Functions
  • Mammals / genetics
  • Models, Genetic*
  • Phylogeny*
  • Point Mutation / genetics
  • Primates / genetics
  • RNA, Ribosomal / genetics

Substances

  • DNA, Mitochondrial
  • RNA, Ribosomal
  • Globins