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A scale-space method for detecting recurrent DNA copy number changes with analytical false discovery rate control

Tumor formation is partially driven by DNA copy number changes, which are typically measured using array comparative genomic hybridization, SNP arrays and DNA sequencing platforms. Many techniques are available for detecting recurring aberrations across multiple tumor samples, including CMAR, STAC,...

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Autores principales: van Dyk, Ewald, Reinders, Marcel J.T., Wessels, Lodewyk F.A.
Formato: Artigo
Lenguaje:Inglês
Publicado: Oxford University Press 2013
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC3643574/
https://ncbi.nlm.nih.gov/pubmed/23476020
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkt155
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