2016
DOI: 10.1038/nrg.2015.28
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Harnessing the power of RADseq for ecological and evolutionary genomics

Abstract: A revolution is occurring in ecological and evolutionary genetics, driven by the development of techniques such as Restriction-site-Associated DNA sequencing (RADseq) that allow relatively low-cost discovery and genotyping of thousands of genetic markers for any species, including nonmodel species. Here we provide an overview of the diverse RADseq techniques that have been developed and highlight some of the research questions these powerful methods can be used to answer. We discuss how technical differences a… Show more

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Cited by 1,207 publications
(1,250 citation statements)
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References 121 publications
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“…Methods for producing reduced representation libraries, such as RAD‐seq, are rapidly evolving, and more than 15 methods exist with variations in data quality, genotyping errors, cost, and the number of loci discovered (reviewed in Andrews, Good, Miller, Luikart, & Hohenlohe, 2016). Furthermore, filtering choices (see figure 2 in Benestan et al., 2016) can greatly influence downstream summary statistics.…”
Section: Genotyping Error and Improving Data Qualitymentioning
confidence: 99%
“…Methods for producing reduced representation libraries, such as RAD‐seq, are rapidly evolving, and more than 15 methods exist with variations in data quality, genotyping errors, cost, and the number of loci discovered (reviewed in Andrews, Good, Miller, Luikart, & Hohenlohe, 2016). Furthermore, filtering choices (see figure 2 in Benestan et al., 2016) can greatly influence downstream summary statistics.…”
Section: Genotyping Error and Improving Data Qualitymentioning
confidence: 99%
“…Many recent studies have used RADseq for genome scans to detect locally adapted loci (reviewed in Arnold et al 2013;Tiffin & Ross-Ibarra 2014;Andrews et al 2016). However, RADseq presents a major challenge for genome scan studies because the approach usually samples only a small proportion of the genome, despite generating hundreds to thousands of polymorphic markers (Fig.…”
Section: -Mike Ehrmantraut Breaking Badmentioning
confidence: 99%
“…Table S1 Recent (January 2015 to April 2016) genome scan studies, which used RAD-seq for genotyping. Andrews et al (2016). Generally, RADseq methods produce DNA libraries for high-throughput sequencing using restriction enzymes that cut at specific motifs throughout the genome.…”
Section: Correction Notementioning
confidence: 99%
“…Additionally, generating microsatellite data that is comparable across laboratories is problematic, which can impede large-scale stock structure and MSA syntheses. In contrast, SNPs typically have lower power per locus relative to microsatellites, but hundreds to thousands of SNP loci can now be rapidly and reliably quantified across large numbers of individuals (Campbell et al, 2015;Ali et al, 2016;Andrews et al, 2016). Additionally, SNPs in coding regions can be used to understand genotype and phenotype linkages and identify loci under selection if adequate genomic and budget resources are available (Hoban et al, 2016;Todd et al, 2016).…”
Section: Expansion Of Molecular Markersmentioning
confidence: 99%