Genome-Wide Detection of Copy Number Variations and Their Association With Distinct Phenotypes in the World’s Sheep

Copy number variations (CNVs) are a major source of structural variation in mammalian genomes. Here, we characterized the genome-wide CNV in 2059 sheep from 67 populations all over the world using the Ovine Infinium HD (600K) SNP BeadChip. We tested their associations with distinct phenotypic traits...

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Detalhes bibliográficos
Publicado no:Front Genet
Main Authors: Salehian-Dehkordi, Hosein, Xu, Ya-Xi, Xu, Song-Song, Li, Xin, Luo, Ling-Yun, Liu, Ya-Jing, Wang, Dong-Feng, Cao, Yin-Hong, Shen, Min, Gao, Lei, Chen, Ze-Hui, Glessner, Joseph T., Lenstra, Johannes A., Esmailizadeh, Ali, Li, Meng-Hua, Lv, Feng-Hua
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2021
Assuntos:
Genetics
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8175073/
https://ncbi.nlm.nih.gov/pubmed/34093663
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2021.670582
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