ArticleBMC genomics2012
Genome wide SNP discovery in flax through next generation sequencing of reduced representation libraries.
Article in BMC genomics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.
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Who cites it
44 citing papers in PubMed, 88 citations in OpenAlex.
- Genome Editing Approaches in Flax (International journal of molecular sciences · 2026Review
- Genomic selection for seed yield enhances flax breeding efficiency.Molecular breeding : new strategies in plant improvement · 2026Article
- Construction and optimization of a genetic transformation system for efficient expression of human insulin-GFP fusion gene in flax.Bioresources and bioprocessing · 2024Article
- Fine-mapping of a major locus for Fusarium wilt resistance in flax (Linum usitatissimum L.).TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2024Article
- History and prospects of flax genetic markers.Frontiers in plant science · 2024Review
- Selection of Flax Genotypes for Pan-Genomic Studies by Sequencing Tagmentation-Based Transcriptome Libraries.Plants (Basel, Switzerland) · 2023Article
- Review
- Genome-wide genetic architecture for plant maturity and drought tolerance in diploid potatoes.Frontiers in genetics · 2023Article
- Development and Complex Application of Methods for the Identification of Mutations in thePlants (Basel, Switzerland) · 2022Article
- Quantitative Trait Locus Mapping of Marsh Spot Disease Resistance in Cranberry Common Bean (International journal of molecular sciences · 2022Article
- Insights into the Genetic Architecture and Genomic Prediction of Powdery Mildew Resistance in Flax (International journal of molecular sciences · 2022Article
- Fine-mapping of a putative glutathione S-transferase (GST) gene responsible for yellow seed colour in flax (Linum usitatissimum).BMC research notes · 2022Article
- Integrated omics approaches for flax improvement under abiotic and biotic stress: Current status and future prospects.Frontiers in plant science · 2022Review
- Genotyping-by-Sequencing inPlants (Basel, Switzerland) · 2021Article
- Mapping Quantitative Trait Loci onto Chromosome-Scale Pseudomolecules in Flax.Methods and protocols · 2020Article
- Genomic Prediction Accuracy of Seven Breeding Selection Traits Improved by QTL Identification in Flax.International journal of molecular sciences · 2020Article
- Flax tubulin and CesA superfamilies represent attractive and challenging targets for a variety of genome- and base-editing applications.Functional & integrative genomics · 2020Review
- The Toolbox for Fiber Flax Breeding: A Pipeline From Gene Expression to Fiber Quality.Frontiers in genetics · 2020Article
- Evaluation of Chemical Composition of Two Linseed Varieties as Sources of Health-Beneficial Substances.Molecules (Basel, Switzerland) · 2019Article
- Characterization of repeated DNA sequences in genomes of blue-flowered flax.BMC evolutionary biology · 2019Article
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Authors and funding
3 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundFlax (Linum usitatissimum L.) is a significant fibre and oilseed crop. Current flax molecular markers, including isozymes, RAPDs, AFLPs and SSRs are of limited use in the construction of high density linkage maps and for association mapping applications due to factors such as low reproducibility, intense labour requirements and/or limited numbers. We report here on the use of a reduced representation library strategy combined with next generation Illumina sequencing for rapid and large scale discovery of SNPs in eight flax genotypes. SNP discovery was performed through in silico analysis of the sequencing data against the whole genome shotgun sequence assembly of flax genotype CDC Bethune. Genotyping-by-sequencing of an F6-derived recombinant inbred line population provided validation of the SNPs.
resultsReduced representation libraries of eight flax genotypes were sequenced on the Illumina sequencing platform resulting in sequence coverage ranging from 4.33 to 15.64X (genome equivalents). Depending on the relatedness of the genotypes and the number and length of the reads, between 78% and 93% of the reads mapped onto the CDC Bethune whole genome shotgun sequence assembly. A total of 55,465 SNPs were discovered with the largest number of SNPs belonging to the genotypes with the highest mapping coverage percentage. Approximately 84% of the SNPs discovered were identified in a single genotype, 13% were shared between any two genotypes and the remaining 3% in three or more. Nearly a quarter of the SNPs were found in genic regions. A total of 4,706 out of 4,863 SNPs discovered in Macbeth were validated using genotyping-by-sequencing of 96 F6 individuals from a recombinant inbred line population derived from a cross between CDC Bethune and Macbeth, corresponding to a validation rate of 96.8%.
conclusionsNext generation sequencing of reduced representation libraries was successfully implemented for genome-wide SNP discovery from flax. The genotyping-by-sequencing approach proved to be efficient for validation. The SNP resources generated in this work will assist in generating high density maps of flax and facilitate QTL discovery, marker-assisted selection, phylogenetic analyses, association mapping and anchoring of the whole genome shotgun sequence.
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