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A Novel Graph-based Algorithm to Infer Recurrent Copy Number Variations in Cancer

Many cancers have been linked to copy number variations (CNVs) in the genomic DNA. Although there are existing methods to analyze CNVs from individual samples, cancer-causing genes are more frequently discovered in regions where CNVs are common among tumor samples, also known as recurrent CNVs. Inte...

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Detalles Bibliográficos
Autores principales:	Chi, Chen, Ajwad, Rasif, Kuang, Qin, Hu, Pingzhao
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Libertas Academica 2016
Materias:	Methodology
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5063805/ https://www.ncbi.nlm.nih.gov/pubmed/27773988 http://dx.doi.org/10.4137/CIN.S39368

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