131 research outputs found

    Stable set meeting every longest path

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    AbstractLaborde, Payan and Xuong conjectured that every digraph has a stable set meeting every longest path. We prove that this conjecture holds for digraphs with stability number at most 2

    Acyclic edge colouring of planar graphs

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    b-coloring is NP-hard on co-bipartite graphs and polytime solvable on tree-cographs

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    A b-coloring of a graph is a proper coloring such that every color class contains a vertex that is adjacent to all other color classes. The b-chromatic number of a graph G, denoted by \chi_b(G), is the maximum number t such that G admits a b-coloring with t colors. A graph G is called b-continuous if it admits a b-coloring with t colors, for every t = \chi(G),\ldots,\chi_b(G), and b-monotonic if \chi_b(H_1) \geq \chi_b(H_2) for every induced subgraph H_1 of G, and every induced subgraph H_2 of H_1. We investigate the b-chromatic number of graphs with stability number two. These are exactly the complements of triangle-free graphs, thus including all complements of bipartite graphs. The main results of this work are the following: - We characterize the b-colorings of a graph with stability number two in terms of matchings with no augmenting paths of length one or three. We derive that graphs with stability number two are b-continuous and b-monotonic. - We prove that it is NP-complete to decide whether the b-chromatic number of co-bipartite graph is at most a given threshold. - We describe a polynomial time dynamic programming algorithm to compute the b-chromatic number of co-trees. - Extending several previous results, we show that there is a polynomial time dynamic programming algorithm for computing the b-chromatic number of tree-cographs. Moreover, we show that tree-cographs are b-continuous and b-monotonic

    A contribution to the second neighborhood problem

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    Seymour's Second Neighborhood Conjecture asserts that every digraph (without digons) has a vertex whose first out-neighborhood is at most as large as its second out-neighborhood. It is proved for tournaments, tournaments missing a matching and tournaments missing a generalized star. We prove this conjecture for classes of digraphs whose missing graph is a comb, a complete graph minus 2 independent edges, or a complete graph minus the edges of a cycle of length 5

    Lower Bounds for the Graph Homomorphism Problem

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    The graph homomorphism problem (HOM) asks whether the vertices of a given nn-vertex graph GG can be mapped to the vertices of a given hh-vertex graph HH such that each edge of GG is mapped to an edge of HH. The problem generalizes the graph coloring problem and at the same time can be viewed as a special case of the 22-CSP problem. In this paper, we prove several lower bound for HOM under the Exponential Time Hypothesis (ETH) assumption. The main result is a lower bound 2Ω(nlog⁥hlog⁥log⁥h)2^{\Omega\left( \frac{n \log h}{\log \log h}\right)}. This rules out the existence of a single-exponential algorithm and shows that the trivial upper bound 2O(nlog⁥h)2^{{\mathcal O}(n\log{h})} is almost asymptotically tight. We also investigate what properties of graphs GG and HH make it difficult to solve HOM(G,H)(G,H). An easy observation is that an O(hn){\mathcal O}(h^n) upper bound can be improved to O(hvc⁥(G)){\mathcal O}(h^{\operatorname{vc}(G)}) where vc⁥(G)\operatorname{vc}(G) is the minimum size of a vertex cover of GG. The second lower bound hΩ(vc⁥(G))h^{\Omega(\operatorname{vc}(G))} shows that the upper bound is asymptotically tight. As to the properties of the "right-hand side" graph HH, it is known that HOM(G,H)(G,H) can be solved in time (f(Δ(H)))n(f(\Delta(H)))^n and (f(tw⁥(H)))n(f(\operatorname{tw}(H)))^n where Δ(H)\Delta(H) is the maximum degree of HH and tw⁥(H)\operatorname{tw}(H) is the treewidth of HH. This gives single-exponential algorithms for graphs of bounded maximum degree or bounded treewidth. Since the chromatic number χ(H)\chi(H) does not exceed tw⁥(H)\operatorname{tw}(H) and Δ(H)+1\Delta(H)+1, it is natural to ask whether similar upper bounds with respect to χ(H)\chi(H) can be obtained. We provide a negative answer to this question by establishing a lower bound (f(χ(H)))n(f(\chi(H)))^n for any function ff. We also observe that similar lower bounds can be obtained for locally injective homomorphisms.Comment: 19 page

    Contraception and screening for cervical and breast cancer in neuromuscular disease: A retrospective study of 50 patients monitored at a clinical reference centre

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    AbstractObjectiveTo analyse contraceptive methods and the extent of screening for breast and cervical cancer in women with neuromuscular disease, compare these results with data and guidelines for the general population and determine the environmental and attitudinal barriers encountered.Patients and methodsA retrospective, descriptive study in a population of female neuromuscular disease patients (aged 20 to 74) monitored at a clinical reference centre.ResultsComplete datasets were available for 49 patients. Seventy percent used contraception (hormonal contraception in most cases). Sixty-eight percent had undergone screening for cervical cancer at some time in the previous 3 years and 100% of the patients over 50 had undergone a mammography. Architectural accessibility and practical problems were the most common barriers to care and were more frequently encountered by wheelchair-bound, ventilated patients.ConclusionsIn general, the patients had good access to contraceptive care and cervical and breast cancer screening. However, specific measures may be useful for the most severely disabled patients

    Nonrepetitive Colouring via Entropy Compression

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    A vertex colouring of a graph is \emph{nonrepetitive} if there is no path whose first half receives the same sequence of colours as the second half. A graph is nonrepetitively kk-choosable if given lists of at least kk colours at each vertex, there is a nonrepetitive colouring such that each vertex is coloured from its own list. It is known that every graph with maximum degree Δ\Delta is cΔ2c\Delta^2-choosable, for some constant cc. We prove this result with c=1c=1 (ignoring lower order terms). We then prove that every subdivision of a graph with sufficiently many division vertices per edge is nonrepetitively 5-choosable. The proofs of both these results are based on the Moser-Tardos entropy-compression method, and a recent extension by Grytczuk, Kozik and Micek for the nonrepetitive choosability of paths. Finally, we prove that every graph with pathwidth kk is nonrepetitively O(k2)O(k^{2})-colourable.Comment: v4: Minor changes made following helpful comments by the referee

    Prognostic significance of cortactin levels in head and neck squamous cell carcinoma: comparison with epidermal growth factor receptor status

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    Cortactin is an actin-binding Src substrate involved in cell motility and invasion. In this study, we sought to examine the prognostic importance of cortactin protein expression in head and neck squamous cell carcinoma (HNSCC). To do so, cortactin and EGF receptor (EGFR) expression was retrospectively evaluated by immunohistochemistry in a tissue microarray composed of 176 HNSCCs with a mean follow-up time of 5 years. Cortactin immunoreactivity was weak to absent in normal epithelial tissue. Overexpression of the protein in 77 out of 176 tumours (44%) was associated with more advanced tumour-node-metastasis stage and higher histologic grade. Cortactin overexpression was associated with significantly increased local recurrence rates (49 vs 28% for high and low expressing carcinomas, respectively), decreased disease-free survival (17 vs 61%), and decreased the 5-year overall survival of (21 vs 58%), independently of the EGFR status. In multivariate analysis, cortactin expression status remained an independent prognostic factor for local recurrence, disease-free survival, and overall survival. Importantly, we identified a subset of patients with cortactin-overexpressing tumours that displayed low EGFR levels and a survival rate that equalled that of patients with tumoral overexpression of both EGFR and cortactin. These findings identify cortactin as a relevant prognostic marker and may have implications for targeted therapies in patients with HNSCC

    A Unified Approach to Distance-Two Colouring of Graphs on Surfaces

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    In this paper we introduce the notion of Σ\Sigma-colouring of a graph GG: For given subsets Σ(v)\Sigma(v) of neighbours of vv, for every v∈V(G)v\in V(G), this is a proper colouring of the vertices of GG such that, in addition, vertices that appear together in some Σ(v)\Sigma(v) receive different colours. This concept generalises the notion of colouring the square of graphs and of cyclic colouring of graphs embedded in a surface. We prove a general result for graphs embeddable in a fixed surface, which implies asymptotic versions of Wegner's and Borodin's Conjecture on the planar version of these two colourings. Using a recent approach of Havet et al., we reduce the problem to edge-colouring of multigraphs, and then use Kahn's result that the list chromatic index is close to the fractional chromatic index. Our results are based on a strong structural lemma for graphs embeddable in a fixed surface, which also implies that the size of a clique in the square of a graph of maximum degree Δ\Delta embeddable in some fixed surface is at most 32 Δ\frac32\,\Delta plus a constant.Comment: 36 page
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