The use of ultra-dense array CGH analysis for the discovery of micro-copy number alterations and gene fusions in the cancer genome

BACKGROUND: Molecular alterations critical to development of cancer include mutations, copy number alterations (amplifications and deletions) as well as genomic rearrangements resulting in gene fusions. Massively parallel next generation sequencing, which enables the discovery of such changes, uses...

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Detalles Bibliográficos
Autores principales: Przybytkowski, Ewa, Ferrario, Cristiano, Basik, Mark
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3041991/
https://www.ncbi.nlm.nih.gov/pubmed/21272361
http://dx.doi.org/10.1186/1755-8794-4-16

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3041991/
https://www.ncbi.nlm.nih.gov/pubmed/21272361
http://dx.doi.org/10.1186/1755-8794-4-16

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