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C(3): Consensus Cancer Driver Gene Caller
Next-generation sequencing has allowed identification of millions of somatic mutations in human cancer cells. A key challenge in interpreting cancer genomes is to distinguish drivers of cancer development among available genetic mutations. To address this issue, we present the first web-based applic...
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| Foilsithe in: | Genomics Proteomics Bioinformatics |
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| Main Authors: | , , , , , , , , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
Elsevier
2019
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6818389/ https://ncbi.nlm.nih.gov/pubmed/31465854 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.gpb.2018.10.004 |
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