2011
DOI: 10.1016/j.gene.2011.04.011
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Analysis of copy number variants in the cattle genome

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Cited by 36 publications
(38 citation statements)
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“…Array CGH and SNP arrays have been used to identify CNVs in cattle and dogs, and the average CNV size has ranged from 33 kb to 275 kb. However, close inspection of the probe spacing of the arrays used in these studies (200 bp to 50 kb) suggests that CNVs of the expected median size and smaller would be missed (Chen et al 2009;Nicholas et al 2009;Fadista et al 2010;Liu et al 2010;Hou et al 2011;Kijas et al 2011;Nicholas et al 2011). Although we failed to identify CNVs in intergenic regions because of the genecentric design of the array, we felt that the benefit of identifying smaller genic CNVs outweighed the identification of larger genic and intergenic CNVs.…”
Section: Discussionmentioning
confidence: 94%
“…Array CGH and SNP arrays have been used to identify CNVs in cattle and dogs, and the average CNV size has ranged from 33 kb to 275 kb. However, close inspection of the probe spacing of the arrays used in these studies (200 bp to 50 kb) suggests that CNVs of the expected median size and smaller would be missed (Chen et al 2009;Nicholas et al 2009;Fadista et al 2010;Liu et al 2010;Hou et al 2011;Kijas et al 2011;Nicholas et al 2011). Although we failed to identify CNVs in intergenic regions because of the genecentric design of the array, we felt that the benefit of identifying smaller genic CNVs outweighed the identification of larger genic and intergenic CNVs.…”
Section: Discussionmentioning
confidence: 94%
“…In addition, the OvineSNP50 BeadChip has fewer probes than other mamalian BeadChips, such as those of humans [42], cattle [43]and pigs [44], and some…”
Section: Accepted Manuscriptmentioning
confidence: 99%
“…SNPs are also inefficient to capture some relevant genome polymorphisms, such as certain types of copy number variation (e.g. Kijas et al, 2011;Fontanesi et al, 2012). Nevertheless, they are quickly replacing microsatellites in paternity testing and genetic diversity studies, due to their robustness, low cost and automatic allele calling.…”
Section: Development Of High-throughput Snp Assays For the Analysis Omentioning
confidence: 99%