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...

Descripción completa

Detalles Bibliográficos
Autores principales: Negro, Sandra S., Millet, Emilie J., Madur, Delphine, Bauland, Cyril, Combes, Valérie, Welcker, Claude, Tardieu, François, Charcosset, Alain, Nicolas, Stéphane D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6636005/
https://www.ncbi.nlm.nih.gov/pubmed/31311506
http://dx.doi.org/10.1186/s12870-019-1926-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6636005/
https://www.ncbi.nlm.nih.gov/pubmed/31311506
http://dx.doi.org/10.1186/s12870-019-1926-4

Ejemplares similares