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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Detalhes bibliográficos
Publicado no:BMC Plant Biol
Main Authors: Negro, Sandra S., Millet, Emilie J., Madur, Delphine, Bauland, Cyril, Combes, Valérie, Welcker, Claude, Tardieu, François, Charcosset, Alain, Nicolas, Stéphane D.
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2019
Assuntos:
Research Article
Acesso em linha: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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