Evidence map›Paper›PMID 19793831›Full record

ArticleMolecular biology and evolution2010

How robust are "isolation with migration" analyses to violations of the im model? A simulation study.

Jared L Strasburg, Loren H Rieseberg

Abstract read
In one paragraph

Article in Molecular biology and evolution, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers.

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75citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

75 citing papers in PubMed.

  1. Article
  2. Bioinformatics advances · 2023
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  5. Highly Replicated Evolution of Parapatric Ecotypes.Molecular biology and evolution · 2021
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  12. Interspecific Divergence of TwoFrontiers in plant science · 2018
    Article
  13. Article
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  15. Article
  16. Geographic extent of introgression inEvolutionary applications · 2017
    Article
  17. Article
  18. Article
  19. Article
  20. Article

15 more citing papers are in PubMed but not listed here.

4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Jared L StrasburgDepartment of Biology, Indiana University, USA. jstrasbu@indiana.edu
Loren H Rieseberg

Funding

Demographics and phylogeography of hybrid speciationF32GM072409 · NIGMS · TRUSTEES OF INDIANA UNIVERSITY · PI STRASBURG, JARED L · 2005 to 2007
$118k
NIGMS NIH HHS 5F32GM072409-02NIGMS NIH HHS F32 GM072409
6 · The paper itself

Abstract

Methods developed over the past decade have made it possible to estimate molecular demographic parameters such as effective population size, divergence time, and gene flow with unprecedented accuracy and precision. However, they make simplifying assumptions about certain aspects of the species' histories and the nature of the genetic data, and it is not clear how robust they are to violations of these assumptions. Here, we use simulated data sets to examine the effects of a number of violations of the "Isolation with Migration" (IM) model, including intralocus recombination, population structure, gene flow from an unsampled species, linkage among loci, and divergent selection, on demographic parameter estimates made using the program IMA. We also examine the effect of having data that fit a nucleotide substitution model other than the two relatively simple models available in IMA. We find that IMA estimates are generally quite robust to small to moderate violations of the IM model assumptions, comparable with what is often encountered in real-world scenarios. In particular, population structure within species, a condition encountered to some degree in virtually all species, has little effect on parameter estimates even for fairly high levels of structure. Likewise, most parameter estimates are robust to significant levels of recombination when data sets are pared down to apparently nonrecombining blocks, although substantial bias is introduced to several estimates when the entire data set with recombination is included. In contrast, a poor fit to the nucleotide substitution model can result in an increased error rate, in some cases due to a predictable bias and in other cases due to an increase in variance in parameter estimates among data sets simulated under the same conditions.

Indexed as

Computer SimulationGene FlowGenetics, PopulationModels, Genetic

Identifiers

PMID19793831
PMCPMC2877552

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.