Ganapathy Ganeshkumar, Uyenoyama Marcy K
National Evolutionary Synthesis Center, Durham, NC 27705-4667, USA.
Theor Popul Biol. 2009 Jun;75(4):346-54. doi: 10.1016/j.tpb.2009.04.003. Epub 2009 Apr 14.
Genomic survey data now permit an unprecedented level of sensitivity in the detection of departures from canonical evolutionary models, including expansions in population size and selective sweeps. Here, we examine the effects of seemingly subtle differences among sampling distributions on goodness of fit analyses of site frequency spectra constructed from single nucleotide polymorphisms. Conditioning on the observation of exactly two alleles in a random sample results in a site frequency spectrum that is independent of the scaled rate of neutral substitution (theta). Other sampling distributions, including conditioning on a single mutational event in the sample genealogy or randomly selecting a single mutation from a genealogy with multiple mutations, have distinct site frequency spectra that show highly significant departures from the predictions of the biallelic model. Some aspects of data filtering may contribute to significant departures of site frequency spectra from expectation, apart from any violation of the standard neutral model.
基因组调查数据现在使得在检测与标准进化模型的偏差方面达到了前所未有的灵敏度,包括种群大小的扩张和选择性清除。在这里,我们研究了抽样分布中看似细微的差异对由单核苷酸多态性构建的位点频率谱的拟合优度分析的影响。以在随机样本中恰好观察到两个等位基因为条件,会产生一个与中性替换的标度率(θ)无关的位点频率谱。其他抽样分布,包括以样本谱系中的单个突变事件为条件或从具有多个突变的谱系中随机选择单个突变,具有不同的位点频率谱,这些谱显示出与双等位基因模型的预测有高度显著的偏差。除了任何对标准中性模型的违反之外,数据过滤的某些方面可能导致位点频率谱与预期有显著偏差。