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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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| Publicado no: | BioData Min |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2015
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| Assuntos: | |
| Acesso em linha: | 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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