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A comparative study of multi-omics integration tools for cancer driver gene identification and tumour subtyping
Oncogenesis and cancer can arise as a consequence of a wide range of genomic aberrations including mutations, copy number alterations, expression changes and epigenetic modifications encompassing multiple omics layers. Integrating genomic, transcriptomic, proteomic and epigenomic datasets via multi-...
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| 出版年: | Brief Bioinform |
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| 主要な著者: | , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Oxford University Press
2019
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7711266/ https://ncbi.nlm.nih.gov/pubmed/31774481 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bib/bbz121 |
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