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...

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Detalles Bibliográficos
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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Research
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

Internet

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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