ArticleGenome biology and evolution2015
Predicting RAD-seq Marker Numbers across the Eukaryotic Tree of Life.
Article in Genome biology and evolution, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.
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Who cites it
16 citing papers in PubMed, 50 citations in OpenAlex.
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- Evaluating restriction enzyme selection for reduced representation sequencing in conservation genomics.Molecular ecology resources · 2025Article
- Population Genomics Analysis with RAD, Reprised: Stacks 2.Methods in molecular biology (Clifton, N.J.) · 2022Article
- OpenTree: A Python Package for Accessing and Analyzing Data from the Open Tree of Life.Systematic biology · 2021Article
- Facilitating population genomics of non-model organisms through optimized experimental design for reduced representation sequencing.BMC genomics · 2021Article
- Double-digest RAD-sequencing: do pre- and post-sequencing protocol parameters impact biological results?Molecular genetics and genomics : MGG · 2021Article
- Article
- Evolutionary selection against short nucleotide sequences in viruses and their related hosts.DNA research : an international journal for rapid publication of reports on genes and genomes · 2020Article
- Population genomics of rapidly invading lionfish in the Caribbean reveals signals of range expansion in the absence of spatial population structure.Ecology and evolution · 2019Article
- Experimental validation of in silico predicted RAD locus frequencies using genomic resources and short read data from a model marine mammal.BMC genomics · 2019Article
- Complex signatures of genomic variation of two non-model marine species in a homogeneous environment.BMC genomics · 2018Article
- Deriving genotypes from RAD-seq short-read data using Stacks.Nature protocols · 2017Article
- Reference-based RADseq resolves robust relationships among closely related species of lichen-forming fungi using metagenomic DNA.Scientific reports · 2017Article
- Article
- Development of a universal and simplified ddRAD library preparation approach for SNP discovery and genotyping in angiosperm plants.Plant methods · 2016Article
Corrections and comments
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Authors and funding
3 authors at 2 institutions in 2 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
High-throughput sequencing of reduced representation libraries obtained through digestion with restriction enzymes--generically known as restriction site associated DNA sequencing (RAD-seq)--is a common strategy to generate genome-wide genotypic and sequence data from eukaryotes. A critical design element of any RAD-seq study is knowledge of the approximate number of genetic markers that can be obtained for a taxon using different restriction enzymes, as this number determines the scope of a project, and ultimately defines its success. This number can only be directly determined if a reference genome sequence is available, or it can be estimated if the genome size and restriction recognition sequence probabilities are known. However, both scenarios are uncommon for nonmodel species. Here, we performed systematic in silico surveys of recognition sequences, for diverse and commonly used type II restriction enzymes across the eukaryotic tree of life. Our observations reveal that recognition sequence frequencies for a given restriction enzyme are strikingly variable among broad eukaryotic taxonomic groups, being largely determined by phylogenetic relatedness. We demonstrate that genome sizes can be predicted from cleavage frequency data obtained with restriction enzymes targeting "neutral" elements. Models based on genomic compositions are also effective tools to accurately calculate probabilities of recognition sequences across taxa, and can be applied to species for which reduced representation data are available (including transcriptomes and neutral RAD-seq data sets). The analytical pipeline developed in this study, PredRAD (https://github.com/phrh/PredRAD), and the resulting databases constitute valuable resources that will help guide the design of any study using RAD-seq or related methods.
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