• DocumentCode
    2192701
  • Title

    Fixed-Parameter Tractable Combinatorial Algorithms for Metabolic Networks Alignments

  • Author

    Cheng, Qiong ; Wei, Jinpeng ; Zelikovsky, Alexander ; Ogihara, Mitsunori

  • Author_Institution
    Dept. of Comput. Sci., Univ. of Miami, Coral Gables, FL, USA
  • fYear
    2010
  • fDate
    13-13 Dec. 2010
  • Firstpage
    679
  • Lastpage
    686
  • Abstract
    The accumulation of high-throughput genomic and proteomic data allows for the reconstruction of the increasingly large and complex metabolic networks. In order to analyze accumulated data and reconstructed networks, it is critical to identify network patterns and evolutionary relations between metabolic networks. But even finding similar networks is computationally challenging. Based on the property of gene duplication and function sharing in biological network, we have formulated the network alignment problem which asks the optimal vertex-to-vertex mapping allowing path contraction, vertex deletion, and vertex insertions. In this paper we present fixed parameter tractable combinatorial algorithms, which take into account the enzymes´ functions and the similarity of arbitrary network topologies such as trees and arbitrary graphs wit hallowing the different types of vertex deletions. The proposed algorithms are fixed parameter tractable in the liner or square of the size of feedback vertex set respectively for the case of disallowing or allowing the deletions. We have developed the web service tool MetNetAligner which aligns metabolic networks. We evaluated our results by the randomizedP-Value computation. In the computation, we followed two standard randomization procedures and further developed two other random graph generators which keep the more stringent and consistent topology constraints. By comparing their distribution of the significant alignment pairs, we observed that the more stringent constraints in the topology the random graph generator has, the more pairs of significant alignments there exist. We also performed pair wise mapping of all pathways for four organisms and found a set of statistically significant pathway similarities. We have applied the network alignment to identifying pathway holes which are resulted by inconsistency and missing enzymes. MetNetAligner is available athttp://\\alla.cs.gsu.edu:8080/MinePW/pages/gmapping/GMMain.html Two ran- - dom graph generations and the list of identified pathway holes are available online.
  • Keywords
    Web services; bioinformatics; combinatorial mathematics; enzymes; gene therapy; genomics; graph theory; proteomics; MetNetAligner; Web service tool; accumulated data analysis; biological network; complex metabolic network; enzyme function; feedback vertex set; fixed parameter tractable combinatorial algorithm; function sharing; gene duplication; high throughput genomic data; metabolic networks alignment; network pattern; network reconstruction; network topology; optimal vertex-to-vertex mapping; pairwise mapping; path contraction; pathway similarity; proteomic data; random graph generator; randomized P-value computation; topology constraint; vertex deletion; vertex insertion; Feedback Vertex Sets; Graph homeomorphism; Network Alignment;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Data Mining Workshops (ICDMW), 2010 IEEE International Conference on
  • Conference_Location
    Sydney, NSW
  • Print_ISBN
    978-1-4244-9244-2
  • Electronic_ISBN
    978-0-7695-4257-7
  • Type

    conf

  • DOI
    10.1109/ICDMW.2010.179
  • Filename
    5693362