Genotyping-by-sequencing and SNP-arrays are complementary for detecting quantitative trait loci by tagging different haplotypes in association studies

BACKGROUND: Single Nucleotide Polymorphism (SNP) array and re-sequencing technologies have different properties (e.g. calling rate, minor allele frequency profile) and drawbacks (e.g. ascertainment bias). This lead us to study their complementarity and the consequences of using them separately or co...

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Bibliografische gegevens
Gepubliceerd in:BMC Plant Biol
Hoofdauteurs: Negro, Sandra S., Millet, Emilie J., Madur, Delphine, Bauland, Cyril, Combes, Valérie, Welcker, Claude, Tardieu, François, Charcosset, Alain, Nicolas, Stéphane D.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: BioMed Central 2019
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Research Article
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6636005/
https://ncbi.nlm.nih.gov/pubmed/31311506
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12870-019-1926-4
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