ISSN:
1432-0541
Keywords:
Computational biology
;
Approximation algorithms
;
Branch- and-bound algorithms
;
Experimental analysis of algorithms
;
Edit distance
;
Permutations
;
Sorting by reversals
;
Chromosome inversions
;
Genome rearrangements
Source:
Springer Online Journal Archives 1860-2000
Topics:
Computer Science
,
Mathematics
Notes:
Abstract Motivated by the problem in computational biology of reconstructing the series of chromosome inversions by which one organism evolved from another, we consider the problem of computing the shortest series of reversals that transform one permutation to another. The permutations describe the order of genes on corresponding chromosomes, and areversal takes an arbitrary substring of elements, and reverses their order. For this problem, we develop two algorithms: a greedy approximation algorithm, that finds a solution provably close to optimal inO(n 2) time and0(n) space forn-element permutations, and a branch- and-bound exact algorithm, that finds an optimal solution in0(mL(n, n)) time and0(n 2) space, wherem is the size of the branch- and-bound search tree, andL(n, n) is the time to solve a linear program ofn variables andn constraints. The greedy algorithm is the first to come within a constant factor of the optimum; it guarantees a solution that uses no more than twice the minimum number of reversals. The lower and upper bounds of the branch- and-bound algorithm are a novel application of maximum-weight matchings, shortest paths, and linear programming. In a series of experiments, we study the performance of an implementation on random permutations, and permutations generated by random reversals. For permutations differing byk random reversals, we find that the average upper bound on reversal distance estimatesk to within one reversal fork〈1/2n andn〈100. For the difficult case of random permutations, we find that the average difference between the upper and lower bounds is less than three reversals forn〈50. Due to the tightness of these bounds, we can solve, to optimality, problems on 30 elements in a few minutes of computer time. This approaches the scale of mitochondrial genomes.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1007/BF01188586
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