A survey of methods and tools to detect recent and strong positive selection.

IF 16.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Accounts of Chemical Research Pub Date : 2017-04-08 eCollection Date: 2017-12-01 DOI:10.1186/s40709-017-0064-0
Pavlos Pavlidis, Nikolaos Alachiotis
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引用次数: 87

Abstract

Positive selection occurs when an allele is favored by natural selection. The frequency of the favored allele increases in the population and due to genetic hitchhiking the neighboring linked variation diminishes, creating so-called selective sweeps. Detecting traces of positive selection in genomes is achieved by searching for signatures introduced by selective sweeps, such as regions of reduced variation, a specific shift of the site frequency spectrum, and particular LD patterns in the region. A variety of methods and tools can be used for detecting sweeps, ranging from simple implementations that compute summary statistics such as Tajima's D, to more advanced statistical approaches that use combinations of statistics, maximum likelihood, machine learning etc. In this survey, we present and discuss summary statistics and software tools, and classify them based on the selective sweep signature they detect, i.e., SFS-based vs. LD-based, as well as their capacity to analyze whole genomes or just subgenomic regions. Additionally, we summarize the results of comparisons among four open-source software releases (SweeD, SweepFinder, SweepFinder2, and OmegaPlus) regarding sensitivity, specificity, and execution times. In equilibrium neutral models or mild bottlenecks, both SFS- and LD-based methods are able to detect selective sweeps accurately. Methods and tools that rely on LD exhibit higher true positive rates than SFS-based ones under the model of a single sweep or recurrent hitchhiking. However, their false positive rate is elevated when a misspecified demographic model is used to represent the null hypothesis. When the correct (or similar to the correct) demographic model is used instead, the false positive rates are considerably reduced. The accuracy of detecting the true target of selection is decreased in bottleneck scenarios. In terms of execution time, LD-based methods are typically faster than SFS-based methods, due to the nature of required arithmetic.

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对检测近期强阳性选择的方法和工具的调查。
当一个等位基因受到自然选择的青睐时,就会出现正选择。受青睐的等位基因在人群中出现的频率增加,由于基因搭便车,邻近的相关变异减少,产生了所谓的选择性扫描。检测基因组中正选择的痕迹是通过搜索选择性扫描引入的特征来实现的,例如变异减少的区域,位点频谱的特定移位,以及该区域的特定LD模式。各种方法和工具可用于检测扫描,从计算汇总统计的简单实现,如田岛D,到使用统计、最大似然、机器学习等组合的更高级的统计方法。在这项调查中,我们提出并讨论了汇总统计和软件工具,并根据它们检测到的选择性扫描特征对它们进行分类,即基于sfs的与基于ld的,以及它们分析全基因组或亚基因组区域的能力。此外,我们总结了四个开源软件版本(SweeD、SweepFinder、SweepFinder2和OmegaPlus)在灵敏度、特异性和执行时间方面的比较结果。在平衡中性模型或轻度瓶颈中,基于SFS和基于ld的方法都能够准确地检测选择性扫描。在单次扫描或反复搭便车模式下,依赖于LD的方法和工具比基于sfs的方法和工具显示出更高的真阳性率。然而,当使用错误指定的人口统计学模型来表示原假设时,他们的假阳性率会升高。当使用正确的(或类似于正确的)人口统计模型时,假阳性率大大降低。在瓶颈情况下,检测选择真实目标的准确性降低。在执行时间方面,基于ld的方法通常比基于sfs的方法快,这是由于所需算法的性质。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Accounts of Chemical Research
Accounts of Chemical Research 化学-化学综合
CiteScore
31.40
自引率
1.10%
发文量
312
审稿时长
2 months
期刊介绍: Accounts of Chemical Research presents short, concise and critical articles offering easy-to-read overviews of basic research and applications in all areas of chemistry and biochemistry. These short reviews focus on research from the author’s own laboratory and are designed to teach the reader about a research project. In addition, Accounts of Chemical Research publishes commentaries that give an informed opinion on a current research problem. Special Issues online are devoted to a single topic of unusual activity and significance. Accounts of Chemical Research replaces the traditional article abstract with an article "Conspectus." These entries synopsize the research affording the reader a closer look at the content and significance of an article. Through this provision of a more detailed description of the article contents, the Conspectus enhances the article's discoverability by search engines and the exposure for the research.
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