Genome-wide detection of copy number variation in Chinese indigenous sheep using an ovine high-density 600 K SNP array

Copy number variants (CNVs) represent a form of genomic structural variation underlying phenotypic diversity. In this study, we used the Illumina Ovine SNP 600 K BeadChip array for genome-wide detection of CNVs in 48 Chinese Tan sheep. A total of 1,296 CNV regions (CNVRs), ranging from 1.2 kb to 2.3...

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Detalles Bibliográficos
Autores principales: Ma, Qing, Liu, Xuexue, Pan, Jianfei, Ma, Lina, Ma, Yuehui, He, Xiaohong, Zhao, Qianjun, Pu, Yabin, Li, Yingkang, Jiang, Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5430420/
https://www.ncbi.nlm.nih.gov/pubmed/28424525
http://dx.doi.org/10.1038/s41598-017-00847-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5430420/
https://www.ncbi.nlm.nih.gov/pubmed/28424525
http://dx.doi.org/10.1038/s41598-017-00847-9

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