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Accounting for linkage disequilibrium in genome scans for selection without individual genotypes: The local score approach

机译:在没有个体基因型的基因组扫描中核糖扫描中的核算:地方得分方法

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Detecting genomic footprints of selection is an important step in the understanding of evolution. Accounting for linkage disequilibrium in genome scans increases detection power, but haplotype-based methods require individual genotypes and are not applicable on pool-sequenced samples. We propose to take advantage of the local score approach to account for linkage disequilibrium in genome scans for selection, cumulating (possibly small) signals from single markers over a genomic segment, to clearly pinpoint a selection signal. Using computer simulations, we demonstrate that this approach detects selection with higher power than several state-of-the-art single-marker, windowing or haplotype-based approaches. We illustrate this on two benchmark data sets including individual genotypes, for which we obtain similar results with the local score and one haplotype-based approach. Finally, we apply the local score approach to Pool-Seq data obtained from a divergent selection experiment on behaviour in quail and obtain precise and biologically coherent selection signals: while competing methods fail to highlight any clear selection signature, our method detects several regions involving genes known to act on social responsiveness or autistic traits. Although we focus here on the detection of positive selection from multiple population data, the local score approach is general and can be applied to other genome scans for selection or other genomewide analyses such as GWAS.
机译:检测选择基因组足迹是了解进化的重要一步。在基因组扫描中核算链接不平衡增加了检测能力,但基于单倍型的方法需要个体基因型,不适用于池测序的样品。我们建议利用当地的评分方法来解释基因组扫描中的联动不平衡,从基因组段中的单个标记累积(可能小)信号,以清楚地确定选择信号。使用计算机模拟,我们证明了这种方法检测到比若干最先进的单标记,窗口或基于单倍型的方法更高的功率。我们在包括单个基因型的两个基准数据集上说明这一点,我们通过局部评分和一种基于单倍型的方法获得类似的结果。最后,我们将本地得分方法应用于从鹌鹑的行为的不同选择实验获得的池-SEQ数据,并获得精确和生物相干的选择信号:虽然竞争方法未能突出任何清晰的选择签名,但我们的方法检测到涉及基因的几个区域已知对社会反应性或自闭症特征起作用。虽然我们在这里专注于从多个人口数据的阳性选择的检测,但是局部得分方法是一般的,并且可以应用于其他基因组扫描,用于选择或其他基因组分析如GWAS。

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