2016
DOI: 10.1186/s12864-016-2447-2
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SNP discovery and genetic mapping using genotyping by sequencing of whole genome genomic DNA from a pea RIL population

Abstract: BackgroundProgress in genetics and breeding in pea still suffers from the limited availability of molecular resources. SNP markers that can be identified through affordable sequencing processes, without the need for prior genome reduction or a reference genome to assemble sequencing data would allow the discovery and genetic mapping of thousands of molecular markers. Such an approach could significantly speed up genetic studies and marker assisted breeding for non-model species.ResultsA total of 419,024 SNPs w… Show more

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Cited by 80 publications
(62 citation statements)
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References 40 publications
(15 reference statements)
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“…Genotype-by-sequencing (GBS) is one next-generation sequencing technique, and is based on the reduction of genome complexity using restriction enzymes23. GBS is characterized as a simple, quick, specific, reproducible technique23, and has been extensively used to identify a large number of SNPs in various model and non-model species25262728.…”
mentioning
confidence: 99%
“…Genotype-by-sequencing (GBS) is one next-generation sequencing technique, and is based on the reduction of genome complexity using restriction enzymes23. GBS is characterized as a simple, quick, specific, reproducible technique23, and has been extensively used to identify a large number of SNPs in various model and non-model species25262728.…”
mentioning
confidence: 99%
“…GBS was originally applied in maize to identify SNP markers in a RIL population [65]. Since then, several studies have been reported in literature for large-scale SNP discovery and genotyping of RILs [68,69], bi-parental mapping population segregating for important agronomical traits [70,71]; ethylmethane sulfonate-(EMS) induced mutant populations [72,73]; and unrelated individuals in small or large size populations [74,75]. All of these efforts, most of which were carried out on vegetable crop species, aimed to have available a high number of SNP data points for concomitant or future genome-wide association studies.…”
Section: Ngs-based Genotyping For Genetic Diversity Evaluationmentioning
confidence: 99%
“…RAD-Seq yields fragments distributed randomly over a genome and is suitable for discovering indels (insertion-deletion polymorphisms), SNVs (single nucleotide variations) and microsatellites simple sequence repeats (SSR). Using RAD-Seq, Boutet et al [57] discovered a total of 419,024 SNVs between at least two of the four pea lines analysed in their work. Pea genetic map constructed by genotyping a subset of 64,754 SNVs on a subpopulation of 48 RILs (recombinant inbred lines) was collinear with previous pea consensus maps and therefore with the M. truncatula genome.…”
Section: Transcript-based Markers and Their Usagementioning
confidence: 99%