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      Combining heterogenous data for prediction of disease related and pharmacogenes.

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          Abstract

          Identifying genetic variants that affect drug response or play a role in disease is an important task for clinicians and researchers. Before individual variants can be explored efficiently for effect on drug response or disease relationships, specific candidate genes must be identified. While many methods rank candidate genes through the use of sequence features and network topology, only a few exploit the information contained in the biomedical literature. In this work, we train and test a classifier on known pharmacogenes from PharmGKB and present a classifier that predicts pharmacogenes on a genome-wide scale using only Gene Ontology annotations and simple features mined from the biomedical literature. Performance of F=0.86, AUC=0.860 is achieved. The top 10 predicted genes are analyzed. Additionally, a set of enriched pharmacogenic Gene Ontology concepts is produced.

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          Author and article information

          Journal
          Pac Symp Biocomput
          Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing
          2335-6936
          2335-6928
          2014
          Affiliations
          [1 ] Computational Bioscience Program, University of Colorado School of Medicine, Aurora, CO 80045, USA. Christopher.Funk@ucdenver.edu.
          Article
          9789814583220_0032 NIHMS544682
          3910248
          24297559
          65796aaa-8fa9-4d0b-9b65-de7f90597b51
          History

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