A survey of analysis software for array-comparative genomic hybridisation studies to detect copy number variation

Copy number variants (CNVs) create a major source of variation among individuals and populations. Array-based comparative genomic hybridisation (aCGH) is a powerful method used to detect and compare the copy numbers of DNA sequences at high resolution along the genome. In recent years, several infor...

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Detalles Bibliográficos
Autores principales: Karimpour-Fard, Anis, Dumas, Laura, Phang, Tzulip, Sikela, James M, Hunter, Lawrence E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Software Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3525224/
https://www.ncbi.nlm.nih.gov/pubmed/20846932
http://dx.doi.org/10.1186/1479-7364-4-6-421

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3525224/
https://www.ncbi.nlm.nih.gov/pubmed/20846932
http://dx.doi.org/10.1186/1479-7364-4-6-421

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