4.7 Article

HitWalker: variant prioritization for personalized functional cancer genomics

Journal

BIOINFORMATICS
Volume 29, Issue 4, Pages 509-510

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/bioinformatics/btt003

Keywords

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Funding

  1. Leukemia & Lymphoma Society [7005-11]
  2. NIH/NCI [5P30CA069533-13, 4R00CA151457-03]
  3. NIH/NCATS V Foundation for Cancer Research [5UL1RR024140]
  4. William Lawrence & Blanche Hughes Foundation, HHMI

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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.

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