1,968 research outputs found

    List circular backbone colouring

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    Graph TheoryInternational audienceA natural generalization of graph colouring involves taking colours from a metric space and insisting that the endpoints of an edge receive colours separated by a minimum distance dictated by properties of the edge. In the q-backbone colouring problem, these minimum distances are either q or 1, depending on whether or not the edge is in the backbone. In this paper we consider the list version of this problem, with particular focus on colours in ℤp - this problem is closely related to the problem of circular choosability. We first prove that the list circular q-backbone chromatic number of a graph is bounded by a function of the list chromatic number. We then consider the more general problem in which each edge is assigned an individual distance between its endpoints, and provide bounds using the Combinatorial Nullstellensatz. Through this result and through structural approaches, we achieve good bounds when both the graph and the backbone belong to restricted families of graphs

    A general framework for coloring problems: old results, new results, and open problems

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    In this survey paper we present a general framework for coloring problems that was introduced in a joint paper which the author presented at WG2003. We show how a number of different types of coloring problems, most of which have been motivated from frequency assignment, fit into this framework. We give a survey of the existing results, mainly based on and strongly biased by joint work of the author with several different groups of coauthors, include some new results, and discuss several open problems for each of the variants

    Backbone Colouring of Graphs

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    Consider an undirected graph G and a subgraph of G, H. A q-backbone k-colouring of (G,H) is a mapping f: V(G) {1, 2, ..., k} such that G is properly coloured and for each edge of H, the colours of its endpoints differ by at least q. The minimum number k for which there is a backbone k-colouring of (G,H) is the backbone chromatic number, BBCq(G,H). It has been proved that backbone k-colouring of (G,T) is at most 4 if G is a connected C4-free planar graph or non-bipartite C5-free planar graph or Cj-free, j∈{6,7,8} planar graph without adjacent triangles. In this thesis we improve the results mentioned above and prove that 2-backbone k-colouring of any connected planar graphs without adjacent triangles is at most 4 by using a discharging method. In the second part of this thesis we further improve these results by proving that for any graph G with χ(G) ≥ 4, BBC(G,T) = χ(G). In fact, we prove the stronger result that a backbone tree T in G exists, such that ∀ uv ∈ T, |f(u)-f(v)|=2 or |f(u)-f(v)| ≥ k-2, k = χ(G). For the case that G is a planar graph, according to Four Colour Theorem, χ(G) = 4; so, BBC(G,T) = 4

    Backbone colorings for networks: tree and path backbones

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    We introduce and study backbone colorings, a variation on classical vertex colorings: Given a graph G=(V,E)G=(V,E) and a spanning subgraph HH of GG (the backbone of GG), a backbone coloring for GG and HH is a proper vertex coloring V→{1,2,…}V\rightarrow \{1,2,\ldots\} of GG in which the colors assigned to adjacent vertices in HH differ by at least two. We study the cases where the backbone is either a spanning tree or a spanning path

    Solving problems on generalized convex graphs via mim-width

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    A bipartite graph G = (A, B, E) is H-convex, for some family of graphs H, if there exists a graph H ∈ H with V (H) = A such that the set of neighbours in A of each b ∈ B induces a connected subgraph of H. Many NP-complete problems become polynomial-time solvable for H-convex graphs when H is the set of paths. In this case, the class of H-convex graphs is known as the class of convex graphs. The underlying reason is that this class has bounded mim-width. We extend the latter result to families of H-convex graphs where (i) H is the set of cycles, or (ii) H is the set of trees with bounded maximum degree and a bounded number of vertices of degree at least 3. As a consequence, we can reprove and strengthen a large number of results on generalized convex graphs known in the literature. To complement result (ii), we show that the mim-width of H-convex graphs is unbounded if H is the set of trees with arbitrarily large maximum degree or an arbitrarily large number of vertices of degree at least 3. In this way we are able to determine complexity dichotomies for the aforementioned graph problems. Afterwards we perform a more refined width-parameter analysis, which shows even more clearly which width parameters are bounded for classes of H-convex graphs

    Vertex and edge covers with clustering properties: complexity and algorithms

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    We consider the concepts of a t-total vertex cover and a t-total edge cover (t≥1), which generalise the notions of a vertex cover and an edge cover, respectively. A t-total vertex (respectively edge) cover of a connected graph G is a vertex (edge) cover S of G such that each connected component of the subgraph of G induced by S has at least t vertices (edges). These definitions are motivated by combining the concepts of clustering and covering in graphs. Moreover they yield a spectrum of parameters that essentially range from a vertex cover to a connected vertex cover (in the vertex case) and from an edge cover to a spanning tree (in the edge case). For various values of t, we present NP-completeness and approximability results (both upper and lower bounds) and FTP algorithms for problems concerned with finding the minimum size of a t-total vertex cover, t-total edge cover and connected vertex cover, in particular improving on a previous FTP algorithm for the latter problem

    An interference-aware virtual clustering paradigm for resource management in cognitive femtocell networks

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    Femtocells represent a promising alternative solution for high quality wireless access in indoor scenarios where conventional cellular system coverage can be poor. They are randomly deployed by the end user, so only post deployment network planning is possible. Furthermore, this uncoordinated deployment creates severe interference to co-located femtocells, especially in dense deployments. This paper presents a new architecture using a generalised virtual cluster femtocell (GVCF) paradigm, which groups together FAP into logical clusters. It guarantees severely interfering and overlapping femtocells are assigned to different clusters. Since each cluster operates on different band of frequencies, the corresponding virtual cluster controller only has to manage its own FAPs, so the overall system complexity is low. The performance of the GVCF algorithm is analysed from both a resource availability and cluster number perspective. Simulation results conclusively corroborate the superior performance of the GVCF model in interference mitigation, particularly in high density FAP scenarios

    The Phyre2 web portal for protein modeling, prediction and analysis

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    Phyre2 is a suite of tools available on the web to predict and analyze protein structure, function and mutations. The focus of Phyre2 is to provide biologists with a simple and intuitive interface to state-of-the-art protein bioinformatics tools. Phyre2 replaces Phyre, the original version of the server for which we previously published a paper in Nature Protocols. In this updated protocol, we describe Phyre2, which uses advanced remote homology detection methods to build 3D models, predict ligand binding sites and analyze the effect of amino acid variants (e.g., nonsynonymous SNPs (nsSNPs)) for a user's protein sequence. Users are guided through results by a simple interface at a level of detail they determine. This protocol will guide users from submitting a protein sequence to interpreting the secondary and tertiary structure of their models, their domain composition and model quality. A range of additional available tools is described to find a protein structure in a genome, to submit large number of sequences at once and to automatically run weekly searches for proteins that are difficult to model. The server is available at http://www.sbg.bio.ic.ac.uk/phyre2. A typical structure prediction will be returned between 30 min and 2 h after submission
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