Abstract

BackgroundRecent advances in genomics have greatly increased research opportunities for non-model species. For wildlife, a growing availability of reference genomes means that population genetics is no longer restricted to a small set of anonymous loci. When used in conjunction with a reference genome, reduced-representation sequencing (RRS) provides a cost-effective method for obtaining reliable diversity information for population genetics. Many software tools have been developed to process RRS data, though few studies of non-model species incorporate genome alignment in calling loci. A commonly-used RRS analysis pipeline, Stacks, has this capacity and so it is timely to compare its utility with existing software originally designed for alignment and analysis of whole genome sequencing data. Here we examine population genetic inferences from two species for which reference-aligned reduced-representation data have been collected. Our two study species are a threatened Australian marsupial (Tasmanian devil Sarcophilus harrisii; declining population) and an Arctic-circle migrant bird (pink-footed goose Anser brachyrhynchus; expanding population). Analyses of these data are compared using Stacks versus two widely-used genomics packages, SAMtools and GATK. We also introduce a custom R script to improve the reliability of single nucleotide polymorphism (SNP) calls in all pipelines and conduct population genetic inferences for non-model species with reference genomes.ResultsAlthough we identified orders of magnitude fewer SNPs in our devil dataset than for goose, we found remarkable symmetry between the two species in our assessment of software performance. For both datasets, all three methods were able to delineate population structure, even with varying numbers of loci. For both species, population structure inferences were influenced by the percent of missing data.ConclusionsFor studies of non-model species with a reference genome, we recommend combining Stacks output with further filtering (as included in our R pipeline) for population genetic studies, paying particular attention to potential impact of missing data thresholds. We recognise SAMtools as a viable alternative for researchers more familiar with this software. We caution against the use of GATK in studies with limited computational resources or time.

Highlights

  • Recent advances in genomics have greatly increased research opportunities for non-model species

  • Biologists who start with a reference assembly may develop familiarity with, and in-house pipelines for, bioinformatic software designed for whole genome sequencing (WGS), such as SAMtools [10] and the Genome Analysis Toolkit (GATK) [11]

  • Within-population diversity We applied our three analysis pipelines (Stacks, SAMtools, GATK; all further processed with the custom R script; Fig. 1) to a total of 131 devil samples and 40 goose samples

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Summary

Introduction

Recent advances in genomics have greatly increased research opportunities for non-model species. Our two study species are a threatened Australian marsupial (Tasmanian devil Sarcophilus harrisii; declining population) and an Arctic-circle migrant bird (pink-footed goose Anser brachyrhynchus; expanding population) Analyses of these data are compared using Stacks versus two widely-used genomics packages, SAMtools and GATK. While RRS provides a cost-effective method of sequencing a large number of genome-wide loci across many individuals, coupling this approach with an assembled reference genome improves the reliability of genotype calls [5] and subsequently improves any downstream inferences [6]. [7,8,9]) In this context, biologists who start with a reference assembly may develop familiarity with, and in-house pipelines for, bioinformatic software designed for whole genome sequencing (WGS), such as SAMtools [10] and the Genome Analysis Toolkit (GATK) [11]. Calibration of GATK SNP calling parameters is highly dependent on known variant datasets [15], making parameterisation problematic for non-model species

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