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[Keyword] hybridization(3hit)

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  • A Multi-Learning Immune Algorithm for Numerical Optimization

    Shuaiqun WANG  Shangce GAO   Aorigele  Yuki TODO  Zheng TANG  

     
    PAPER-Numerical Analysis and Optimization

      Vol:
    E98-A No:1
      Page(s):
    362-377

    The emergence of nature-inspired algorithms (NIA) is a great milestone in the field of computational intelligence community. As one of the NIAs, the artificial immune algorithm (AIS) mimics the principles of the biological immune system, and has exhibited its effectiveness, implicit parallelism, flexibility and applicability when solving various engineering problems. Nevertheless, AIS still suffers from the issues of evolution premature, local minima trapping and slow convergence due to its inherent stochastic search dynamics. Much effort has been made to improve the search performance of AIS from different aspects, such as population diversity maintenance, adaptive parameter control, etc. In this paper, we propose a novel multi-learning operator into the AIS to further enrich the search dynamics of the algorithm. A framework of embedding multiple commonly used mutation operators into the antibody evolution procedure is also established. Four distinct learning operators including baldwinian learning, cauchy mutation, gaussian mutation and lateral mutation are selected to merge together as a multi-learning operator. It can be expected that the multi-learning operator can effectively balance the exploration and exploitation of the search by enriched dynamics. To verify its performance, the proposed algorithm, which is called multi-learning immune algorithm (MLIA), is applied on a number of benchmark functions. Experimental results demonstrate the superiority of the proposed algorithm in terms of convergence speed and solution quality.

  • Improved Clonal Selection Algorithm Combined with Ant Colony Optimization

    Shangce GAO  Wei WANG  Hongwei DAI  Fangjia LI  Zheng TANG  

     
    PAPER-Biocybernetics, Neurocomputing

      Vol:
    E91-D No:6
      Page(s):
    1813-1823

    Both the clonal selection algorithm (CSA) and the ant colony optimization (ACO) are inspired by natural phenomena and are effective tools for solving complex problems. CSA can exploit and explore the solution space parallely and effectively. However, it can not use enough environment feedback information and thus has to do a large redundancy repeat during search. On the other hand, ACO is based on the concept of indirect cooperative foraging process via secreting pheromones. Its positive feedback ability is nice but its convergence speed is slow because of the little initial pheromones. In this paper, we propose a pheromone-linker to combine these two algorithms. The proposed hybrid clonal selection and ant colony optimization (CSA-ACO) reasonably utilizes the superiorities of both algorithms and also overcomes their inherent disadvantages. Simulation results based on the traveling salesman problems have demonstrated the merit of the proposed algorithm over some traditional techniques.

  • Efficient Methods for Determining DNA Probe Orders

    Hiro ITO  Kazuo IWAMA  Takeyuki TAMURA  

     
    PAPER

      Vol:
    E89-A No:5
      Page(s):
    1292-1298

    In STS-based mapping, it is necessary to obtain the correct order of probes in a DNA sequence from a given set of fragments or an equivalently a hybridization matrix A. It is well-known that the problem is formulated as the combinatorial problem of obtaining a permutation of A's columns so that the resulting matrix has a consecutive-one property. If the data (the hybridization matrix) is error free and includes enough information, then the above column order uniquely determines the correct order of the probes. Unfortunately this does not hold if the data include errors, and this has been a popular research target in computational biology. Even if there is no error, ambiguities in the probe order may still remain. This in fact happens because of the lack of some information regarding the data, but almost no further investigation has previously been made. In this paper, we define a measure of such imperfectness of the data as the minimum amount of the additional fragments that are needed to uniquely fix the probe order. Polynomial-time algorithms to compute such additional fragments of the minimum cost are presented. A computer simulation using genes of human chromosome 20 is also noted.