Genome-Wide Detection of CNVs and Association With Body Weight in Sheep Based on 600K SNP Arrays

Copy number variations (CNVs) are important genomic structural variations and can give rise to significant phenotypic diversity. Herein, we used high-density 600K SNP arrays to detect CNVs in two synthetic lines of sheep (DS and SHH) and in Hu sheep (a local Chinese breed). A total of 919 CNV region...

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Detalles Bibliográficos
Autores principales: Wang, Zhipeng, Guo, Jing, Guo, Yuanyuan, Yang, Yonglin, Teng, Teng, Yu, Qian, Wang, Tao, Zhou, Meng, Zhu, Qiusi, Wang, Wenwen, Zhang, Qin, Yang, Hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7297042/
https://www.ncbi.nlm.nih.gov/pubmed/32582291
http://dx.doi.org/10.3389/fgene.2020.00558

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7297042/
https://www.ncbi.nlm.nih.gov/pubmed/32582291
http://dx.doi.org/10.3389/fgene.2020.00558

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