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Copy number analysis of the low-copy repeats at the primate NPHP1 locus by array comparative genomic hybridization
Array comparative genomic hybridization (aCGH) has been widely used to detect copy number variants (CNVs) in both research and clinical settings. A customizable aCGH platform may greatly facilitate copy number analyses in genomic regions with higher-order complexity, such as low-copy repeats (LCRs)....
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| Udgivet i: | Genom Data |
|---|---|
| Main Authors: | , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Elsevier
2016
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4872932/ https://ncbi.nlm.nih.gov/pubmed/27222811 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.gdata.2016.04.008 |
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