Title :
Tractable Cases of
-Bounded Parsimony Haplotyping
Author :
Keijsper, Judith ; Oosterwijk, Tim
Author_Institution :
Dept. of Math., Tech. Univ. Eindhoven, Eindhoven, Netherlands
Abstract :
Parsimony haplotyping is the problem of finding a set of haplotypes of minimum cardinality that explains a given set of genotypes, where a genotype is explained by two haplotypes if it can be obtained as a combination of the two. This problem is NP-complete in the general case, but polynomially solvable for (k, l)-bounded instances for certain k and l. Here, k denotes the maximum number of ambiguous sites in any genotype, and l is the maximum number of genotypes that are ambiguous at the same site. Only the complexity of the (*, 2)-bounded problem is still unknown, where * denotes no restriction. It has been proved that (*, 2)-bounded instances have compatibility graphs that can be constructed from cliques and circuits by pasting along an edge. In this paper, we give a constructive proof of the fact that (*, 2)-bounded instances are polynomially solvable if the compatibility graph is constructed by pasting cliques, trees and circuits along a bounded number of edges. We obtain this proof by solving a slightly generalized problem on circuits, trees and cliques respectively, and arguing that all possible combinations of optimal solutions for these graphs that are pasted along a bounded number of edges can be enumerated efficiently.
Keywords :
bioinformatics; cellular biophysics; genetics; genomics; trees (mathematics); (*, 2)-bounded parsimony haplotyping; (k,l)-bounded instances; ambiguous sites; compatibility graph; generalized problem; genotypes; minimum cardinality haplotypes; pasting cliques; tractable cases; trees; Bioinformatics; Complexity theory; Computational biology; IEEE transactions; Polynomials; Sociology; Vectors; Drug design; graph; haplotyping; health; hereditary disease; matching problem; path partition; polynomial time algorithm; shortest path;
Journal_Title :
Computational Biology and Bioinformatics, IEEE/ACM Transactions on
DOI :
10.1109/TCBB.2014.2352031