Molecular Ecology · 2013 · 193 citations · 58 references
Life SciencesGeneticsMolecular GeneticsConservation GeneticsGenomicsPopulation GeneticsConservation GenomicsContig ConstructionDna SequencingHigh-throughput GenotypingNext-generation SequencingPopulation GenomicsAdmixture InferenceIntrogression AnalysisPaired-end SequencingShort-read SequencingSingle Nucleotide Polymorphism ArraysSingle-nucleotide Polymorphism AnalysisSingle-nucleotide Polymorphism VariationSnp Arrays
Rapid and inexpensive methods for genomewide single nucleotide polymorphism (SNP) discovery and genotyping are urgently needed for population management and conservation. In hybridized populations, genomic techniques that can identify and genotype thousands of species-diagnostic markers would allow precise estimates of population- and individual-level admixture as well as identification of 'super invasive' alleles, which show elevated rates of introgression above the genomewide background (likely due to natural selection). Techniques like restriction-site-associated DNA (RAD) sequencing can discover and genotype large numbers of SNPs, but they have been limited by the length of continuous sequence data they produce with Illumina short-read sequencing. We present a novel approach, overlapping paired-end RAD sequencing, to generate RAD contigs of >300-400 bp. These contigs provide sufficient flanking sequence for design of high-throughput SNP genotyping arrays and strict filtering to identify duplicate paralogous loci. We applied this approach in five populations of native westslope cutthroat trout that previously showed varying (low) levels of admixture from introduced rainbow trout (RBT). We produced 77 141 RAD contigs and used these data to filter and genotype 3180 previously identified species-diagnostic SNP loci. Our population-level and individual-level estimates of admixture were generally consistent with previous microsatellite-based estimates from the same individuals. However, we observed slightly lower admixture estimates from genomewide markers, which might result from natural selection against certain genome regions, different genomic locations for microsatellites vs. RAD-derived SNPs and/or sampling error from the small number of microsatellite loci (n = 7). We also identified candidate adaptive super invasive alleles from RBT that had excessively high admixture proportions in hybridized cutthroat trout populations.
58
Velvet: Algorithms for de novo short read assembly using de Bruijn graphs
Daniel R. Zerbino, Ewan Birney · Genome Research · 2008 · 9.7K citations · Full text
CAP3: A DNA Sequence Assembly Program
Xiaoqiu Huang, Anup Madan · Genome Research · 1999 · 5.3K citations · Full text
Rapid SNP Discovery and Genetic Mapping Using Sequenced RAD Markers
Nathan A. Baird, Paul D. Etter, Tressa S. Atwood et al. · PLoS ONE · 2008 · 3.5K citations · Full text