Detection of recurrent rearrangement breakpoints from copy number data

BACKGROUND: Copy number variants (CNVs), including deletions, amplifications, and other rearrangements, are common in human and cancer genomes. Copy number data from array comparative genome hybridization (aCGH) and next-generation DNA sequencing is widely used to measure copy number variants. Compa...

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Detalles Bibliográficos
Autores principales: Ritz , Anna, Paris, Pamela L, Ittmann, Michael M, Collins, Colin, Raphael, Benjamin J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3112242/
https://www.ncbi.nlm.nih.gov/pubmed/21510904
http://dx.doi.org/10.1186/1471-2105-12-114

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3112242/
https://www.ncbi.nlm.nih.gov/pubmed/21510904
http://dx.doi.org/10.1186/1471-2105-12-114

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