Genome-wide analysis of CNVs in three populations of Tibetan sheep using whole-genome resequencing

Copy number variation (CNV), an important source of genomic structural variation, can disturb genetic structure, dosage, regulation and expression, and is associated with phenotypic diversity and adaptation to local environments in mammals. In the present study, 24 resequencing datasets were used to...

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Detalles Bibliográficos
Autores principales: Hu, Linyong, Zhang, Liangzhi, Li, Qi, Liu, Hongjin, Xu, Tianwei, Zhao, Na, Han, Xueping, Xu, Shixiao, Zhao, Xinquan, Zhang, Cunfang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9490000/
https://www.ncbi.nlm.nih.gov/pubmed/36160022
http://dx.doi.org/10.3389/fgene.2022.971464

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9490000/
https://www.ncbi.nlm.nih.gov/pubmed/36160022
http://dx.doi.org/10.3389/fgene.2022.971464

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