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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Detalles Bibliográficos
Autores principales: Yuan, Bo, Liu, Pengfei, Rogers, Jeffrey, Lupski, James R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Data in Brief
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4872932/
https://www.ncbi.nlm.nih.gov/pubmed/27222811
http://dx.doi.org/10.1016/j.gdata.2016.04.008

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4872932/
https://www.ncbi.nlm.nih.gov/pubmed/27222811
http://dx.doi.org/10.1016/j.gdata.2016.04.008

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