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Genome-wide detection of copy number variation in American mink using whole-genome sequencing
BACKGROUND: Copy number variations (CNVs) represent a major source of genetic diversity and contribute to the phenotypic variation of economically important traits in livestock species. In this study, we report the first genome-wide CNV analysis of American mink using whole-genome sequence data from...
Autores principales: | Davoudi, Pourya, Do, Duy Ngoc, Rathgeber, Bruce, Colombo, Stefanie M., Sargolzaei, Mehdi, Plastow, Graham, Wang, Zhiquan, Karimi, Karim, Hu, Guoyu, Valipour, Shafagh, Miar, Younes |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9468235/ https://www.ncbi.nlm.nih.gov/pubmed/36096727 http://dx.doi.org/10.1186/s12864-022-08874-1 |
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