Combined Analysis of SNP Array Data Identifies Novel CNV Candidates and Pathways in Ependymoma and Mesothelioma

Copy number variation is a class of structural genomic modifications that includes the gain and loss of a specific genomic region, which may include an entire gene. Many studies have used low-resolution techniques to identify regions that are frequently lost or amplified in cancer. Usually, research...

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Detalles Bibliográficos
Autores principales: Wajnberg, Gabriel, Carvalho, Benilton S., Ferreira, Carlos G., Passetti, Fabio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4491549/
https://www.ncbi.nlm.nih.gov/pubmed/26185765
http://dx.doi.org/10.1155/2015/902419

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4491549/
https://www.ncbi.nlm.nih.gov/pubmed/26185765
http://dx.doi.org/10.1155/2015/902419

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