Genomic variants with a key role in causing cancer or affecting the response to cancer
therapeutics need to be identified so that they can be targeted for therapy. The transFIC tool aims
to identify somatic point mutations that drive cancer in sequencing projects.
This package is
available as a web service, a stand-alone program and a website. It improves the functional
prediction scores generated by popular established prediction tools and will be useful to cancer
researchers.See research article: http://genomemedicine.com/content/4/11/89