Abstract

High-throughput genomic sequencing allows to disentangle the evolutionary forces acting in populations. Among evolutionary forces, positive selection has received a lot of attention because it is related to the adaptation of populations in their environments, both biotic and abiotic. Positive selection, also known as Darwinian 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, neighboring linked variation diminishes, creating so-called selective sweeps. Such a process leaves traces in genomes that can be detected in a future time point. 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 linkage disequilibrium (LD) patterns in the region. A variety of approaches can be used for detecting selective sweeps, ranging from simple implementations that compute summary statistics to more advanced statistical approaches, e.g., Bayesian approaches, maximum-likelihood-based methods, and machine learning methods. In this chapter, we discuss selective sweep detection methodologies on the basis of their capacity to analyze whole genomes or just subgenomic regions, and on the specific polymorphism patterns they exploit as selective sweep signatures. We also summarize the results of comparisons among five open-source software releases (SweeD, SweepFinder, SweepFinder2, OmegaPlus, and RAiSD) regarding sensitivity, specificity, and execution times. Furthermore, we test and discuss machine learning methods and present a thorough performance analysis. In equilibrium neutral models or mild bottlenecks, most methods are able to detect selective sweeps accurately. Methods and tools that rely on linkage disequilibrium (LD) rather than single SNPs exhibit higher true positive rates than the site frequency spectrum (SFS)-based methods 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 build the distribution of the statistic under the null hypothesis. Both LD and SFS-based approaches suffer from decreased accuracy on localizing the true target of selection in bottleneck scenarios. Furthermore, we present an extensive analysis of the effects of gene flow on selective sweep detection, a problem that has been understudied in selective sweep literature.

Highlights

  • High-throughput genomic sequencing allows to disentangle the evolutionary forces acting in populations

  • The genetic diversity is maintained due to recombination in genomic regions that are in the proximity of a selective sweep: single nucleotide polymorphisms (SNP) are not generated by novel mutations, but they are old mutations that escaped selection because of recombination

  • It is important to note that the aforementioned signatures of a selective sweep are predicted when (1) fixation of the beneficial mutation has just been completed; (2) recombination rate is positive, i.e., the chromosome is recombining; (3) the population size is approximately constant over time; (4) the population is isolated; (5) no gene conversion has occurred in the proximity of the beneficial mutation

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Summary

Introduction

High-throughput genomic sequencing allows to disentangle the evolutionary forces acting in populations. The frequency of the favored allele increases in the population and, due to genetic hitchhiking, neighboring linked variation diminishes, creating so-called selective sweeps Such a process leaves traces in genomes that can be detected in a future time point. Methods and tools that rely on linkage disequilibrium (LD) rather than single SNPs exhibit higher true positive rates than the site frequency spectrum (SFS)based methods under the model of a single sweep or recurrent hitchhiking. Their false positive rate is elevated when a misspecified demographic model is used to build the distribution of the statistic under the null hypothesis. A long-term goal is that the genes that experienced recent and strong positive selection could be identified and the associated functions and phenotypes characterized

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