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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...

詳細記述

保存先:
書誌詳細
出版年:Heredity (Edinb)
主要な著者: Liu, Aoxing, Lund, Mogens Sandø, Boichard, Didier, Karaman, Emre, Fritz, Sebastien, Aamand, Gert Pedersen, Nielsen, Ulrik Sander, Wang, Yachun, Su, Guosheng
フォーマット: Artigo
言語:Inglês
出版事項: Springer International Publishing 2019
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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