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Inferring causal genomic alterations in breast cancer using gene expression data
BACKGROUND: One of the primary objectives in cancer research is to identify causal genomic alterations, such as somatic copy number variation (CNV) and somatic mutations, during tumor development. Many valuable studies lack genomic data to detect CNV; therefore, methods that are able to infer CNVs f...
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| Główni autorzy: | , , , , , , , , |
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| Format: | Artigo |
| Język: | Inglês |
| Wydane: |
BioMed Central
2011
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| Hasła przedmiotowe: | |
| Dostęp online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3162519/ https://ncbi.nlm.nih.gov/pubmed/21806811 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1752-0509-5-121 |
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