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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Detalles Bibliográficos
Autores principales: Gómez-Rueda, Hugo, Martínez-Ledesma, Emmanuel, Martínez-Torteya, Antonio, Palacios-Corona, Rebeca, Trevino, Victor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4625638/
https://www.ncbi.nlm.nih.gov/pubmed/26516350
http://dx.doi.org/10.1186/s13040-015-0065-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4625638/
https://www.ncbi.nlm.nih.gov/pubmed/26516350
http://dx.doi.org/10.1186/s13040-015-0065-1

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