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A Composite-Likelihood Method for Detecting Incomplete Selective Sweep from Population Genomic Data

机译:一种基于种群基因组数据的不完全选择性扫描检测的复合似然方法

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摘要

Adaptive evolution occurs as beneficial mutations arise and then increase in frequency by positive natural selection. How, when, and where in the genome such evolutionary events occur is a fundamental question in evolutionary biology. It is possible to detect ongoing positive selection or an incomplete selective sweep in species with sexual reproduction because, when a beneficial mutation is on the way to fixation, homologous chromosomes in the population are divided into two groups: one carrying the beneficial allele with very low polymorphism at nearby linked loci and the other carrying the ancestral allele with a normal pattern of sequence variation. Previous studies developed long-range haplotype tests to capture this difference between two groups as the signal of an incomplete selective sweep. In this study, we propose a composite-likelihood-ratio (CLR) test for detecting incomplete selective sweeps based on the joint sampling probabilities for allele frequencies of two groups as a function of strength of selection and recombination rate. Tested against simulated data, this method yielded statistical power and accuracy in parameter estimation that are higher than the iHS test and comparable to the more recently developed nSL test. This procedure was also applied to African Drosophila melanogaster population genomic data to detect candidate genes under ongoing positive selection. Upon visual inspection of sequence polymorphism, candidates detected by our CLR method exhibited clear haplotype structures predicted under incomplete selective sweeps. Our results suggest that different methods capture different aspects of genetic information regarding incomplete sweeps and thus are partially complementary to each other.
机译:当有益的突变出现时,就会发生适应性进化,然后通过积极的自然选择增加频率。这种进化事件如何,何时以及在基因组中的何处发生是进化生物学中的一个基本问题。可以检测到有性繁殖物种正在进行的正选择或不完全选择扫描,因为当有益的突变进入固定的过程时,种群中的同源染色体分为两组:一组携带非常低的有益等位基因多态性位于附近的连锁基因座,另一个带有祖先等位基因,具有正常的序列变异模式。先前的研究开发了远程单倍型测试,以捕获两组之间的这种差异作为不完全选择性扫描的信号。在这项研究中,我们提出了基于两个组的等位基因频率联合抽样概率作为选择强度和重组率的函数的复合似然比(CLR)测试,以检测不完全的选择性扫描。经过对模拟数据的测试,该方法产生的统计能力和参数估计的准确性高于iHS测试,可与最近开发的nSL测试相比。该程序还应用于非洲果蝇种群基因组数据,以检测正在进行的阳性选择下的候选基因。目视检查序列多态性后,通过我们的CLR方法检测到的候选物显示出在不完全的选择性扫描下预测的清晰单倍型结构。我们的结果表明,不同的方法可以捕获与不完全扫描有关的遗传信息的不同方面,因此可以部分互补。

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