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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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| 出版年: | Heredity (Edinb) |
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| 主要な著者: | , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Springer International Publishing
2019
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| 主題: | |
| オンライン・アクセス: | 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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