Genome-wide copy number variant analysis reveals variants associated with 10 diverse production traits in Holstein cattle

BACKGROUND: Copy number variation (CNV) is an important type of genetic variation contributing to phenotypic differences among mammals and may serve as an alternative molecular marker to single nucleotide polymorphism (SNP) for genome-wide association study (GWAS). Recently, GWAS analysis using CNV...

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Detalles Bibliográficos
Autores principales: Zhou, Yang, Connor, Erin E., Wiggans, George R., Lu, Yongfang, Tempelman, Robert J., Schroeder, Steven G., Chen, Hong, Liu, George E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5930521/
https://www.ncbi.nlm.nih.gov/pubmed/29716533
http://dx.doi.org/10.1186/s12864-018-4699-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5930521/
https://www.ncbi.nlm.nih.gov/pubmed/29716533
http://dx.doi.org/10.1186/s12864-018-4699-5

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