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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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| 出版年: | Cancer Inform |
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| 主要な著者: | , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Libertas Academica
2016
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| 主題: | |
| オンライン･アクセス: | 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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