HitWalker: variant prioritization for personalized functional cancer genomics.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 23303510.
- Also identified by DOI 10.1093/bioinformatics/btt003 and PMC identifier 3570211.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Determining the functional relevance of identified sequence variants in cancer is a prerequisite to ultimately matching specific therapies with individual patients. This level of mechanistic understanding requires integration of genomic information with complementary functional analyses to identify oncogenic targets and relies on the development of computational frameworks to aid in the prioritization and visualization of these diverse data types. In response to this, we have developed HitWalker, which prioritizes patient variants relative to their weighted proximity to functional assay results in a protein-protein interaction network. It is highly extensible, allowing incorporation of diverse data types to refine prioritization. In addition to a ranked list of variants, we have also devised a simple shortest path-based approach of visualizing the results in an intuitive manner to provide biological interpretation. The program, documentation and example data are available as an R package from www.biodevlab.org/HitWalker.html.
Medical subject headings
- Genetic Variation
- Neoplasms
- Software