10 research outputs found

    Polynomial Delay Algorithm for Listing Minimal Edge Dominating sets in Graphs

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    The Transversal problem, i.e, the enumeration of all the minimal transversals of a hypergraph in output-polynomial time, i.e, in time polynomial in its size and the cumulated size of all its minimal transversals, is a fifty years old open problem, and up to now there are few examples of hypergraph classes where the problem is solved. A minimal dominating set in a graph is a subset of its vertex set that has a non empty intersection with the closed neighborhood of every vertex. It is proved in [M. M. Kant\'e, V. Limouzy, A. Mary, L. Nourine, On the Enumeration of Minimal Dominating Sets and Related Notions, In Revision 2014] that the enumeration of minimal dominating sets in graphs and the enumeration of minimal transversals in hypergraphs are two equivalent problems. Hoping this equivalence can help to get new insights in the Transversal problem, it is natural to look inside graph classes. It is proved independently and with different techniques in [Golovach et al. - ICALP 2013] and [Kant\'e et al. - ISAAC 2012] that minimal edge dominating sets in graphs (i.e, minimal dominating sets in line graphs) can be enumerated in incremental output-polynomial time. We provide the first polynomial delay and polynomial space algorithm that lists all the minimal edge dominating sets in graphs, answering an open problem of [Golovach et al. - ICALP 2013]. Besides the result, we hope the used techniques that are a mix of a modification of the well-known Berge's algorithm and a strong use of the structure of line graphs, are of great interest and could be used to get new output-polynomial time algorithms.Comment: proofs simplified from previous version, 12 pages, 2 figure

    Beyond Hypergraph Dualization

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    International audienceThis problem concerns hypergraph dualization and generalization to poset dualization. A hypergraph H = (V, E) consists of a finite collection E of sets over a finite set V , i.e. E ⊆ P(V) (the powerset of V). The elements of E are called hyperedges, or simply edges. A hypergraph is said simple if none of its edges is contained within another. A transversal (or hitting set) of H is a set T ⊆ V that intersects every edge of E. A transversal is minimal if it does not contain any other transversal as a subset. The set of all minimal transversal of H is denoted by T r(H). The hypergraph (V, T r(H)) is called the transversal hypergraph of H. Given a simple hypergraph H, the hypergraph dualization problem (Trans-Enum for short) concerns the enumeration without repetitions of T r(H). The Trans-Enum problem can also be formulated as a dualization problem in posets. Let (P, ≤) be a poset (i.e. ≤ is a reflexive, antisymmetric, and transitive relation on the set P). For A ⊆ P , ↓ A (resp. ↑ A) is the downward (resp. upward) closure of A under the relation ≤ (i.e. ↓ A is an ideal and ↑ A a filter of (P, ≤)). Two antichains (B + , B −) of P are said to be dual if ↓ B + ∪ ↑ B − = P and ↓ B + ∩ ↑ B − = ∅. Given an implicit description of a poset P and an antichain B + (resp. B −) of P , the poset dualization problem (Dual-Enum for short) enumerates the set B − (resp. B +), denoted by Dual(B +) = B − (resp. Dual(B −) = B +). Notice that the function dual is self-dual or idempotent, i.e. Dual(Dual(B)) = B

    Structural and functional analysis of cellular networks with CellNetAnalyzer

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    BACKGROUND: Mathematical modelling of cellular networks is an integral part of Systems Biology and requires appropriate software tools. An important class of methods in Systems Biology deals with structural or topological (parameter-free) analysis of cellular networks. So far, software tools providing such methods for both mass-flow (metabolic) as well as signal-flow (signalling and regulatory) networks are lacking. RESULTS: Herein we introduce CellNetAnalyzer, a toolbox for MATLAB facilitating, in an interactive and visual manner, a comprehensive structural analysis of metabolic, signalling and regulatory networks. The particular strengths of CellNetAnalyzer are methods for functional network analysis, i.e. for characterising functional states, for detecting functional dependencies, for identifying intervention strategies, or for giving qualitative predictions on the effects of perturbations. CellNetAnalyzer extends its predecessor FluxAnalyzer (originally developed for metabolic network and pathway analysis) by a new modelling framework for examining signal-flow networks. Two of the novel methods implemented in CellNetAnalyzer are discussed in more detail regarding algorithmic issues and applications: the computation and analysis (i) of shortest positive and shortest negative paths and circuits in interaction graphs and (ii) of minimal intervention sets in logical networks. CONCLUSION: CellNetAnalyzer provides a single suite to perform structural and qualitative analysis of both mass-flow- and signal-flow-based cellular networks in a user-friendly environment. It provides a large toolbox with various, partially unique, functions and algorithms for functional network analysis.CellNetAnalyzer is freely available for academic use

    Urinary biomarkers of smokers’ exposure to tobacco smoke constituents in tobacco products assessment: a fit for purpose approach

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