Genome-wide copy number variation (CNV) detection in Nelore cattle reveals highly frequent variants in genome regions harboring QTLs affecting production traits

BACKGROUND: Copy number variations (CNVs) have been shown to account for substantial portions of observed genomic variation and have been associated with qualitative and quantitative traits and the onset of disease in a number of species. Information from high-resolution studies to detect, character...

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Detalles Bibliográficos
Autores principales: da Silva, Joaquim Manoel, Giachetto, Poliana Fernanda, da Silva, Luiz Otávio, Cintra, Leandro Carrijo, Paiva, Samuel Rezende, Yamagishi, Michel Eduardo Beleza, Caetano, Alexandre Rodrigues
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4907077/
https://www.ncbi.nlm.nih.gov/pubmed/27297173
http://dx.doi.org/10.1186/s12864-016-2752-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4907077/
https://www.ncbi.nlm.nih.gov/pubmed/27297173
http://dx.doi.org/10.1186/s12864-016-2752-9

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