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  • A Polynomial Time Algorithm for Finding a Minimally Generalized Linear Interval Graph Pattern

    Hitoshi YAMASAKI  Takayoshi SHOUDAI  

     
    PAPER

      Vol:
    E92-D No:2
      Page(s):
    120-129

    A graph is an interval graph if and only if each vertex in the graph can be associated with an interval on the real line such that any two vertices are adjacent in the graph exactly when the corresponding intervals have a nonempty intersection. A number of interesting applications for interval graphs have been found in the literature. In order to find structural features common to structural data which can be represented by intervals, this paper proposes new interval graph structured patterns, called linear interval graph patterns, and a polynomial time algorithm for finding a minimally generalized linear interval graph pattern explaining a given finite set of interval graphs.

  • 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.