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A Novel Graph-based Algorithm to Infer Recurrent Copy Number Variations in Cancer
Many cancers have been linked to copy number variations (CNVs) in the genomic DNA. Although there are existing methods to analyze CNVs from individual samples, cancer-causing genes are more frequently discovered in regions where CNVs are common among tumor samples, also known as recurrent CNVs. Inte...
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| Izdano u: | Cancer Inform |
|---|---|
| Glavni autori: | , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Libertas Academica
2016
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5063805/ https://ncbi.nlm.nih.gov/pubmed/27773988 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4137/CIN.S39368 |
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