How Robust Are "Isolation with Migration" Analyses to Violations of the IM Model? A Simulation Study

被引:200
作者
Strasburg, Jared L. [1 ]
Rieseberg, Loren H. [1 ,2 ]
机构
[1] Indiana Univ, Dept Biol, Bloomington, IN 47405 USA
[2] Univ British Columbia, Dept Bot, Vancouver, BC, Canada
基金
加拿大自然科学与工程研究理事会; 美国国家卫生研究院;
关键词
historical demography; introgression; divergence time; effective population size; simulations; isolation with migration; MAXIMUM-LIKELIHOOD-ESTIMATION; EFFECTIVE POPULATION SIZES; GENE FLOW; DIVERGENCE TIMES; COALESCENCE TIME; SITES; PHYLOGENIES; SPECIATION; SEQUENCES; HISTORY;
D O I
10.1093/molbev/msp233
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:297 / 310
页数:14
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