Identification of copy number variation in Tibetan sheep using whole genome resequencing reveals evidence of genomic selection

BACKGROUND: Copy number variation (CNV) is an important source of structural variation in the mammalian genome. CNV assays present a new method to explore the genomic diversity of environmental adaptations in animals and plants and genes associated with complex traits. In this study, the genome-wide...

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Detalles Bibliográficos
Autores principales: Shi, Huibin, Li, Taotao, Su, Manchun, Wang, Huihui, Li, Qiao, Lang, Xia, Ma, Youji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10510117/
https://www.ncbi.nlm.nih.gov/pubmed/37726692
http://dx.doi.org/10.1186/s12864-023-09672-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10510117/
https://www.ncbi.nlm.nih.gov/pubmed/37726692
http://dx.doi.org/10.1186/s12864-023-09672-z

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