Abstract

BackgroundResearch over the last 10 years highlights the increasing importance of hybridization between species as a major force structuring the evolution of genomes and potentially providing raw material for adaptation by natural and/or sexual selection. Fueled by research in a few model systems where phenotypic hybrids are easily identified, research into hybridization and introgression (the flow of genes between species) has exploded with the advent of whole-genome sequencing and emerging methods to detect the signature of hybridization at the whole-genome or chromosome level. Amongst these are a general class of methods that utilize patterns of single-nucleotide polymorphisms (SNPs) across a tree as markers of hybridization. These methods have been applied to a variety of genomic systems ranging from butterflies to Neanderthals to detect introgression, however, when employed at a fine genomic scale these methods do not perform well to quantify introgression in small sample windows.ResultsWe introduce a novel method to detect introgression by combining two widely used statistics: pairwise nucleotide diversity dxy and Patterson’s D. The resulting statistic, the distance fraction (df), accounts for genetic distance across possible topologies and is designed to simultaneously detect and quantify introgression. We also relate our new method to the recently published fd and incorporate these statistics into the powerful genomics R-package PopGenome, freely available on GitHub (pievos101/PopGenome) and the Comprehensive R Archive Network (CRAN). The supplemental material contains a wide range of simulation studies and a detailed manual how to perform the statistics within the PopGenome framework.ConclusionWe present a new distance based statistic df that avoids the pitfalls of Patterson’s D when applied to small genomic regions and accurately quantifies the fraction of introgression (f) for a wide range of simulation scenarios.

Highlights

  • Research over the last 10 years highlights the increasing importance of hybridization between species as a major force structuring the evolution of genomes and potentially providing raw material for adaptation by natural and/or sexual selection

  • Assuming the outgroup O is fixed for allele A, derived alleles (B) in P3, when shared with either P2 or P1, act as a marker of introgression leading to Pfeifer and Kapan BMC Bioinformatics (2019) 20:207 the following patterns: ABBA or BABA respectively

  • We found that df outperforms or is essentially equivalent to the fd estimate to measure the real fraction of introgression for most of the studied ranges of simulation cases

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Summary

Introduction

Research over the last 10 years highlights the increasing importance of hybridization between species as a major force structuring the evolution of genomes and potentially providing raw material for adaptation by natural and/or sexual selection. Fueled by research in a few model systems where phenotypic hybrids are identified, research into hybridization and introgression (the flow of genes between species) has exploded with the advent of whole-genome sequencing and emerging methods to detect the signature of hybridization at the whole-genome or chromosome level. Amongst these are a general class of methods that utilize patterns of single-nucleotide polymorphisms (SNPs) across a tree as markers of hybridization. An excess of either pattern, ABBA or BABA represents a difference from the 50:50 ratio expected from incomplete lineage sorting and represents a signal that can be used to detect introgression

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