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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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Dades bibliogràfiques
Publicat a:Heredity (Edinb)
Autors principals: Liu, Aoxing, Lund, Mogens Sandø, Boichard, Didier, Karaman, Emre, Fritz, Sebastien, Aamand, Gert Pedersen, Nielsen, Ulrik Sander, Wang, Yachun, Su, Guosheng
Format: Artigo
Idioma:Inglês
Publicat: Springer International Publishing 2019
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6906477/
https://ncbi.nlm.nih.gov/pubmed/31278370
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41437-019-0246-7
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