Genome-wide detection of copy number variations using high-density SNP genotyping platforms in Holsteins

@inproceedings{Jiang2012GenomewideDO,
  title={Genome-wide detection of copy number variations using high-density SNP genotyping platforms in Holsteins},
  author={Li Jiang and Jicai Jiang and Jie Yang and Xuan Liu and Jiying Wang and Haifei Wang and Xiangdong Ding and Jian-feng Liu and Qin Zhang},
  booktitle={BMC Genomics},
  year={2012}
}
Copy number variations (CNVs) are widespread in the human or animal genome and are a significant source of genetic variation, which has been demonstrated to play an important role in phenotypic diversity. Advances in technology have allowed for identification of a large number of CNVs in cattle. Comprehensive explore novel CNVs in the bovine genome would provide valuable information for functional analyses of genome structural variation and facilitating follow-up association studies between… CONTINUE READING
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