Abstract
Genomic variants with a key role in causing cancer or affecting the response to cancertherapeutics need to be identified so that they can be targeted for therapy. The transFIC tool aimsto identify somatic point mutations that drive cancer in sequencing projects. This package isavailable as a web service, a stand-alone program and a website. It improves the functionalprediction scores generated by popular established prediction tools and will be useful to cancerresearchers.See research article: http://genomemedicine.com/content/4/11/89.
| Original language | English |
|---|---|
| Article number | 88 |
| Journal | Genome Medicine |
| Volume | 4 |
| Issue number | 11 |
| DOIs |
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| State | Published - 26 Nov 2012 |
| Externally published | Yes |
Bibliographical note
Funding Information:It has come to our attention that there is an error in the Acknowledgements section of our article [1]. e Acknowledgements section should read: SE is supported by the European Union through the IRG program. e results published here are in whole or part based upon data generated by e Cancer Genome Atlas pilot project established by the NCI and NHGRI. Information about TCGA and the investigators and institutions who constitute the TCGA research network can be found at the project website [2].
Funding
It has come to our attention that there is an error in the Acknowledgements section of our article [1]. e Acknowledgements section should read: SE is supported by the European Union through the IRG program. e results published here are in whole or part based upon data generated by e Cancer Genome Atlas pilot project established by the NCI and NHGRI. Information about TCGA and the investigators and institutions who constitute the TCGA research network can be found at the project website [2].
| Funders | Funder number |
|---|---|
| European Commission |
