[HTML][HTML] Genome-wide detection of copy number variations using high-density SNP genotyping platforms in Holsteins
Abstract Background Copy number variations (CNVs) are widespread in the human or
animal genome and are a significant source of genetic variation, which has been …
animal genome and are a significant source of genetic variation, which has been …
[HTML][HTML] Genome-wide identification of copy number variations in Chinese Holstein
L Jiang, J Jiang, J Wang, X Ding, J Liu, Q Zhang - PloS one, 2012 - journals.plos.org
Recent studies of mammalian genomes have uncovered the vast extent of copy number
variations (CNVs) that contribute to phenotypic diversity. Compared to SNP, a CNV can …
variations (CNVs) that contribute to phenotypic diversity. Compared to SNP, a CNV can …
[HTML][HTML] Genome-wide detection of copy number variations and their association with distinct phenotypes in the world's sheep
H Salehian-Dehkordi, YX Xu, SS Xu, X Li, LY Luo… - Frontiers in …, 2021 - frontiersin.org
Copy number variations (CNVs) are a major source of structural variation in mammalian
genomes. Here, we characterized the genome-wide CNV in 2059 sheep from 67 …
genomes. Here, we characterized the genome-wide CNV in 2059 sheep from 67 …
[HTML][HTML] Genome-wide detection of copy number variation in Chinese indigenous sheep using an ovine high-density 600 K SNP array
Q Ma, X Liu, J Pan, L Ma, Y Ma, X He, Q Zhao, Y Pu… - Scientific reports, 2017 - nature.com
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 …
phenotypic diversity. In this study, we used the Illumina Ovine SNP 600 K BeadChip array for …
A genome‐wide scan for copy number variations using high‐density single nucleotide polymorphism array in Simmental cattle
Copy number variations (CNV s) have recently been identified as promising sources of
genetic variation, complementary to single nucleotide polymorphisms (SNP s). As a result …
genetic variation, complementary to single nucleotide polymorphisms (SNP s). As a result …
[HTML][HTML] Genomic characteristics of cattle copy number variations
Background Copy number variation (CNV) represents another important source of genetic
variation complementary to single nucleotide polymorphism (SNP). High-density SNP array …
variation complementary to single nucleotide polymorphism (SNP). High-density SNP array …
[HTML][HTML] Genome-wide detection of CNVs and association with body weight in sheep based on 600K SNP arrays
Z Wang, J Guo, Y Guo, Y Yang, T Teng, Q Yu… - Frontiers in …, 2020 - frontiersin.org
Copy number variations (CNVs) are important genomic structural variations and can give
rise to significant phenotypic diversity. Herein, we used high-density 600K SNP arrays to …
rise to significant phenotypic diversity. Herein, we used high-density 600K SNP arrays to …
[HTML][HTML] Copy number variants in the sheep genome detected using multiple approaches
GM Jenkins, ME Goddard, MA Black, R Brauning… - BMC genomics, 2016 - Springer
Abstract Background Copy number variants (CNVs) are a type of polymorphism found to
underlie phenotypic variation, both in humans and livestock. Most surveys of CNV in …
underlie phenotypic variation, both in humans and livestock. Most surveys of CNV in …
[HTML][HTML] Genome-wide analysis reveals differential selection involved with copy number variation in diverse Chinese Cattle
L Yang, L Xu, B Zhu, H Niu, W Zhang, J Miao, X Shi… - Scientific reports, 2017 - nature.com
Copy number variations (CNVs) are defined as deletions, insertions, and duplications
between two individuals of a species. To investigate the diversity and population-genetic …
between two individuals of a species. To investigate the diversity and population-genetic …
[HTML][HTML] A genome-wide detection of copy number variations using SNP genotyping arrays in swine
Abstract Background Copy Number Variations (CNVs) have been shown important in both
normal phenotypic variability and disease susceptibility, and are increasingly accepted as …
normal phenotypic variability and disease susceptibility, and are increasingly accepted as …