• DocumentCode
    2838550
  • Title

    Solving Haplotype Reconstruction Problem in MEC Model with Hybrid Information Fusion

  • Author

    Asgarian, Ehsan ; Moeinzadeh, M-Hossein ; Habibi, Jafar ; Sharifian-R, Sarah ; Rasooli-V, Ammar ; Najafi-A, Amir

  • Author_Institution
    Dept. of Comput. Eng., Sharif Univ. of Technol., Tehran
  • fYear
    2008
  • fDate
    8-10 Sept. 2008
  • Firstpage
    214
  • Lastpage
    218
  • Abstract
    Single nucleotide polymorphisms (SNPs), a single DNA base varying from one individual to another, are believed to be the most frequent form responsible for genetic differences. Genotype is the conflated information of a pair of haplotypes on homologous chromosomes. Although haplotypes have more information for disease associating than individual SNPs and genotype, it is substantially more difficult to determine haplotypes through experiments. Hence, computational methods which can reduce the cost of determining haplotypes become attractive alternatives. MEC, as a standard model for haplotype reconstruction, is fed by fragments as input to infer the best pair of haplotypes with minimum error to be corrected. It is proved that haplotype reconstruction in MEC model is a NP-Hard problem. Thus, reducing running time and obtaining acceptable result are desired by researchers. Heuristic algorithms and different clustering methods are employed to achieve these goals. In this paper, the idea of combining different methods is presented. A hybrid model, which is employed the efficiency of different serial and parallel models, is suggested. FCA, K-means and neural network are considered as its component. K-means clustering method is used to improve neural network efficiency. Then the results are compared in different datasets.
  • Keywords
    biocomputing; computational complexity; genetics; neural nets; pattern clustering; sensor fusion; DNA; K-means clustering; NP-hard problem; genetic differences; genotype; haplotype reconstruction; information fusion; neural network; single nucleotide polymorphisms; Biological cells; Clustering algorithms; Clustering methods; Costs; DNA; Diseases; Error correction; Genetics; NP-hard problem; Neural networks;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Computer Modeling and Simulation, 2008. EMS '08. Second UKSIM European Symposium on
  • Conference_Location
    Liverpool
  • Print_ISBN
    978-0-7695-3325-4
  • Electronic_ISBN
    978-0-7695-3325-4
  • Type

    conf

  • DOI
    10.1109/EMS.2008.97
  • Filename
    4625274