Improvement of genomic prediction by integrating additional single nucleotide polymorphisms selected from imputed whole genome sequencing data

The availability of whole genome sequencing (WGS) data enables the discovery of causative single nucleotide polymorphisms (SNPs) or SNPs in high linkage disequilibrium with causative SNPs. This study investigated effects of integrating SNPs selected from imputed WGS data into the data of 54K chip on...

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Detalles Bibliográficos
Autores principales: Liu, Aoxing, Lund, Mogens Sandø, Boichard, Didier, Karaman, Emre, Fritz, Sebastien, Aamand, Gert Pedersen, Nielsen, Ulrik Sander, Wang, Yachun, Su, Guosheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6906477/
https://www.ncbi.nlm.nih.gov/pubmed/31278370
http://dx.doi.org/10.1038/s41437-019-0246-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6906477/
https://www.ncbi.nlm.nih.gov/pubmed/31278370
http://dx.doi.org/10.1038/s41437-019-0246-7

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