Genomic prediction using imputed whole-genome sequence data in Holstein Friesian cattle

BACKGROUND: In contrast to currently used single nucleotide polymorphism (SNP) panels, the use of whole-genome sequence data is expected to enable the direct estimation of the effects of causal mutations on a given trait. This could lead to higher reliabilities of genomic predictions compared to tho...

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Detalles Bibliográficos
Autores principales: van Binsbergen, Rianne, Calus, Mario P. L., Bink, Marco C. A. M., van Eeuwijk, Fred A., Schrooten, Chris, Veerkamp, Roel F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4574568/
https://www.ncbi.nlm.nih.gov/pubmed/26381777
http://dx.doi.org/10.1186/s12711-015-0149-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4574568/
https://www.ncbi.nlm.nih.gov/pubmed/26381777
http://dx.doi.org/10.1186/s12711-015-0149-x

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