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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Bibliographische Detailangaben
Veröffentlicht in:Genom Data
Hauptverfasser: Yuan, Bo, Liu, Pengfei, Rogers, Jeffrey, Lupski, James R.
Format: Artigo
Sprache:Inglês
Veröffentlicht: Elsevier 2016
Schlagworte:
Data in Brief
Online Zugang: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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