Literature DB >> 27825765

Rate matrix estimation from site frequency data.

Conrad J Burden1, Yurong Tang2.   

Abstract

A procedure is described for estimating evolutionary rate matrices from observed site frequency data. The procedure assumes (1) that the data are obtained from a constant size population evolving according to a stationary Wright-Fisher or decoupled Moran model; (2) that the data consist of a multiple alignment of a moderate number of sequenced genomes drawn randomly from the population; and (3) that within the genome a large number of independent, neutral sites evolving with a common mutation rate matrix can be identified. No restrictions are imposed on the scaled rate matrix other than that the off-diagonal elements are positive, their sum is ≪1, and that the rows of the matrix sum to zero. In particular the rate matrix is not assumed to be reversible. The key to the method is an approximate stationary solution to the diffusion limit, forward Kolmogorov equation for neutral evolution in the limit of low mutation rates.
Copyright © 2016 Elsevier Inc. All rights reserved.

Keywords:  Decoupled Moran; Evolutionary rate matrices; Multi-allele Wright–Fisher; Neutral evolution

Mesh:

Year:  2016        PMID: 27825765     DOI: 10.1016/j.tpb.2016.10.001

Source DB:  PubMed          Journal:  Theor Popul Biol        ISSN: 0040-5809            Impact factor:   1.570


  2 in total

1.  The stationary distribution of a sample from the Wright-Fisher diffusion model with general small mutation rates.

Authors:  Conrad J Burden; Robert C Griffiths
Journal:  J Math Biol       Date:  2018-11-13       Impact factor: 2.259

2.  The transition distribution of a sample from a Wright-Fisher diffusion with general small mutation rates.

Authors:  Conrad J Burden; Robert C Griffiths
Journal:  J Math Biol       Date:  2019-09-17       Impact factor: 2.259

  2 in total

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