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Integration and comparison of different genomic data for outcome prediction in cancer

BACKGROUND: In cancer, large-scale technologies such as next-generation sequencing and microarrays have produced a wide number of genomic features such as DNA copy number alterations (CNA), mRNA expression (EXPR), microRNA expression (MIRNA), and DNA somatic mutations (MUT), among others. Several an...

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Dettagli Bibliografici
Pubblicato in:BioData Min
Autori principali: Gómez-Rueda, Hugo, Martínez-Ledesma, Emmanuel, Martínez-Torteya, Antonio, Palacios-Corona, Rebeca, Trevino, Victor
Natura: Artigo
Lingua:Inglês
Pubblicazione: BioMed Central 2015
Soggetti:
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC4625638/
https://ncbi.nlm.nih.gov/pubmed/26516350
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13040-015-0065-1
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