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Array CGH-based detection of CNV regions and their potential association with reproduction and other economic traits in Holsteins
BACKGROUND: Copy number variations (CNVs) are structural variants consisting of large-scale insertions and deletions of genomic fragments. Exploring CNVs and estimating their effects on phenotypes are useful for genome selection but remain challenging in the livestock. RESULTS: We identified 1043 CN...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6407259/ https://www.ncbi.nlm.nih.gov/pubmed/30845913 http://dx.doi.org/10.1186/s12864-019-5552-1 |