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A Likelihood Approach for Uncovering Selective Sweep Signatures from Haplotype Data

机译:一种从单倍型数据中发现选择性扫描特征的似然法

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摘要

Selective sweeps are frequent and varied signatures in the genomes of natural populations, and detecting them is consequently important in understanding mechanisms of adaptation by natural selection. Following a selective sweep, haplotypic diversity surrounding the site under selection decreases, and this deviation from the background pattern of variation can be applied to identify sweeps. Multiple methods exist to locate selective sweeps in the genome from haplotype data, but none leverages the power of a model-based approach to make their inference. Here, we propose a likelihood ratio test statistic T to probe whole-genome polymorphism data sets for selective sweep signatures. Our framework uses a simple but powerful model of haplotype frequency spectrum distortion to find sweeps and additionally make an inference on the number of presently sweeping haplotypes in a population. We found that the T statistic is suitable for detecting both hard and soft sweeps across a variety of demographic models, selection strengths, and ages of the beneficial allele. Accordingly, we applied the T statistic to variant calls from European and sub-Saharan African human populations, yielding primarily literature-supported candidates, including LCT , RSPH3 , and ZNF211 in CEU, SYT1 , RGS18 , and NNT in YRI, and HLA genes in both populations. We also searched for sweep signatures in Drosophila melanogaster , finding expected candidates at Ace , Uhg1 , and Pimet . Finally, we provide open-source software to compute the T statistic and the inferred number of presently sweeping haplotypes from whole-genome data.
机译:选择性扫描是自然种群基因组中频繁且变化多端的特征,因此检测它们对于理解自然选择的适应机制非常重要。在选择性扫描之后,所选位点周围的单倍型多样性减少,并且这种与背景变异模式的偏差可用于识别扫描。有多种方法可以从单倍型数据中定位基因组中的选择性扫描,但没有一种方法利用基于模型的方法的力量进行推断。在这里,我们提出了一个似然比检验统计量T来探测全基因组多态性数据集的选择性扫描特征。我们的框架使用一个简单但强大的单倍型频谱失真模型来查找扫描,并额外推断群体中当前扫描的单倍型的数量。我们发现 T 统计量适用于检测各种人口统计模型、选择强度和有益等位基因年龄的硬扫描和软扫描。因此,我们将 T 统计量应用于来自欧洲和撒哈拉以南非洲人群的变异检出,主要产生文献支持的候选者,包括 CEU 中的 LCT、RSPH3 和 ZNF211、YRI 中的 SYT1、RGS18 和 NNT 以及两个群体中的 HLA 基因。我们还在黑腹果蝇中搜索了扫描特征,在 Ace、Uhg1 和 Pimet 找到了预期的候选者。最后,我们提供了开源软件来计算T统计量和从全基因组数据中推断出的当前扫描单倍型的数量。

著录项

  • 来源
    《Molecular biology and evolution》 |2020年第10期|3023-3046|共24页
  • 作者单位

    Department of Biology, Pennsylvania State University, University Park;

    Molecular, Cellular, and Integrative Biosciences, Huck Institutes of the Life Sciences, Pennsylvania State University, University Park;

    Department of Computer and Electrical Engineering and Computer Science, Florida Atlantic University;

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  • 原文格式 PDF
  • 正文语种 英语
  • 中图分类
  • 关键词

    maximum likelihood; selective sweep; haplotype;

    机译:最大可能性;选择性扫描;单倍型;
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