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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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Dettagli Bibliografici
Pubblicato in:Heredity (Edinb)
Autori principali: Liu, Aoxing, Lund, Mogens Sandø, Boichard, Didier, Karaman, Emre, Fritz, Sebastien, Aamand, Gert Pedersen, Nielsen, Ulrik Sander, Wang, Yachun, Su, Guosheng
Natura: Artigo
Lingua:Inglês
Pubblicazione: Springer International Publishing 2019
Soggetti:
Accesso online: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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