Identification of rare germline copy number variations over-represented in five human cancer types

BACKGROUND: Copy number variations (CNVs) are increasingly recognized as significant disease susceptibility markers in many complex disorders including cancer. The availability of a large number of chromosomal copy number profiles in both malignant and normal tissues in cancer patients presents an o...

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Detalles Bibliográficos
Autores principales: Park, Richard W, Kim, Tae-Min, Kasif, Simon, Park, Peter J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4381456/
https://www.ncbi.nlm.nih.gov/pubmed/25644941
http://dx.doi.org/10.1186/s12943-015-0292-6

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