2015
DOI: 10.1101/028837
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RAD Capture (Rapture): Flexible and efficient sequence-based genotyping

Abstract: Massively parallel sequencing has revolutionized many areas of biology but sequencing large amounts of DNA in many individuals is cost-prohibitive and unnecessary for many studies.Genomic complexity reduction techniques such as sequence capture and restriction enzyme- (which was not peer-reviewed) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity.

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Cited by 49 publications
(61 citation statements)
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“…In this study, we used a new RAD sequencing protocol (Ali et al 2016) to generate a high-quality genomic data set capable of identifying many polymorphisms in DHP. Using our data set, we were able to successfully characterize genetic variation within DHP and build a SNP panel to be used as a genetic monitoring resource.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…In this study, we used a new RAD sequencing protocol (Ali et al 2016) to generate a high-quality genomic data set capable of identifying many polymorphisms in DHP. Using our data set, we were able to successfully characterize genetic variation within DHP and build a SNP panel to be used as a genetic monitoring resource.…”
Section: Discussionmentioning
confidence: 99%
“…In total, we sequenced 32 pupfish individuals: 24 DHP, four AMP and four OWP (sampling details given in Appendix S1, Supporting information). DNA was extracted from fin clips using an Ampure bead-based protocol, and RAD libraries were constructed using the PstI restriction enzyme and a new RAD protocol described in Ali et al (2016). De novo loci discovery and contig extension were carried out via custom PERL scripts (Miller et al 2012), the alignment program Novoalign and the genome assembler PRICE (Ruby et al 2013) (Appendix S1, Supporting information).…”
Section: Sampling Sequence Generation and Rad Loci Discoverymentioning
confidence: 99%
“…Genome scans on 219 individuals were conducted following the BestRAD library preparation protocol with some modifications (Ali et al 2016). 100 ng of DNA was digested using the SbfI restriction enzyme (New England Biolabs, USA) and fragments were ligated with SbfI adapters prepared with biotinylated ends.…”
Section: Snp Discovery and Snp Filteringmentioning
confidence: 99%
“…We extracted DNA from tissue samples (total n = 3149 individuals) and genotyped individuals as described in . In short, we conducted restriction site-associated DNA (RAD) capture (Ali et al 2016) and sequenced libraries using HiSeq (Illumina, San Diego, California, USA). We randomly sampled one read at each single nucleotide polymorphism (SNP) per individual.…”
Section: Summarizing Variation In Migratory Vs Resident Allele Frequmentioning
confidence: 99%