• DocumentCode
    2414526
  • Title

    seGOsa: Software environment for gene ontology-driven similarity assessment

  • Author

    Zheng, Huiru ; Azuaje, Francisco ; Wang, Haiying

  • Author_Institution
    Sch. of Comput. & Math., Univ. of Ulster, Newtownabbey, UK
  • fYear
    2010
  • fDate
    18-21 Dec. 2010
  • Firstpage
    539
  • Lastpage
    542
  • Abstract
    In recent years there has been a growing trend towards the adoption of ontologies to support comprehensive, large-scale functional genomics research. This paper introduces seGOsa, a user-friendly cross-platform system to support large-scale assessment of Gene Ontology (GO)-driven similarity among gene products. Using information-theoretic approaches, the system exploits both topological features of the GO (i.e., between-term relationships in the hierarchy) and statistical features of the model organism databases annotated to the GO (i.e., term frequency) to assess functional similarity among gene products. Based on the assumption that the more information two terms share in common, the more similar they are, three GO-driven similarity measures (Resnik´s, Lin´s and Jiang´s metrics) have been implemented to measure between-term similarity within each of the GO hierarchies. Meanwhile, seGOsa offers two approaches (simple and highest average similarity) to assessing the similarity between gene products based on the aggregation of between-term similarities. The program is freely available for non-profit use on request from the authors.
  • Keywords
    bioinformatics; genetics; genomics; ontologies (artificial intelligence); topology; cross-platform system; gene ontology; large-scale assessment; large-scale functional genomic research; model organism database; seGOsa; similarity assessment; software environment; statistical features; Bioinformatics; Databases; Gene expression; Genomics; Ontologies; Semantics; Gene Ontology; Semantic similarity; information content;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Bioinformatics and Biomedicine (BIBM), 2010 IEEE International Conference on
  • Conference_Location
    Hong Kong
  • Print_ISBN
    978-1-4244-8306-8
  • Electronic_ISBN
    978-1-4244-8307-5
  • Type

    conf

  • DOI
    10.1109/BIBM.2010.5706624
  • Filename
    5706624