Colouring exact distance graphs of chordal graphs

For a graph $G=(V,E)$ and positive integer $p$, the exact distance-$p$ graph $G^{[\natural p]}$ is the graph with vertex set $V$ and with an edge between vertices $x$ and $y$ if and only if $x$ and $y$ have distance $p$. Recently, there has been an effort to obtain bounds on the chromatic number $\chi(G^{[\natural p]})$ of exact distance-$p$ graphs for $G$ from certain classes of graphs. In particular, if a graph $G$ has tree-width $t$, it has been shown that $\chi(G^{[\natural p]}) \in \mathcal{O}(p^{t-1})$ for odd $p$, and $\chi(G^{[\natural p]}) \in \mathcal{O}(p^{t}\Delta(G))$ for even $p$. We show that if $G$ is chordal and has tree-width $t$, then $\chi(G^{[\natural p]}) \in \mathcal{O}(p\, t^2)$ for odd $p$, and $\chi(G^{[\natural p]}) \in \mathcal{O}(p\, t^2 \Delta(G))$ for even $p$. If we could show that for every graph $H$ of tree-width $t$ there is a chordal graph $G$ of tree-width $t$ which contains $H$ as an isometric subgraph (i.e., a distance preserving subgraph), then our results would extend to all graphs of tree-width $t$. While we cannot do this, we show that for every graph $H$ of genus $g$ there is a graph $G$ which is a triangulation of genus $g$ and contains $H$ as an isometric subgraph.Comment: 11 pages, 2 figures. Versions 2 and 3 include minor changes, which arise from reviewers' comment

Reconstruction/Non-reconstruction Thresholds for Colourings of General Galton-Watson Trees

The broadcasting models on trees arise in many contexts such as discrete mathematics, biology statistical physics and cs. In this work, we consider the colouring model. A basic question here is whether the root's assignment affects the distribution of the colourings at the vertices at distance h from the root. This is the so-called "reconstruction problem". For a d-ary tree it is well known that d/ln (d) is the reconstruction threshold. That is, for k=(1+eps)d/ln(d) we have non-reconstruction while for k=(1-eps)d/ln(d) we have. Here, we consider the largely unstudied case where the underlying tree is chosen according to a predefined distribution. In particular, our focus is on the well-known Galton-Watson trees. This model arises naturally in many contexts, e.g. the theory of spin-glasses and its applications on random Constraint Satisfaction Problems (rCSP). The aforementioned study focuses on Galton-Watson trees with offspring distribution B(n,d/n), i.e. the binomial with parameters n and d/n, where d is fixed. Here we consider a broader version of the problem, as we assume general offspring distribution, which includes B(n,d/n) as a special case. Our approach relates the corresponding bounds for (non)reconstruction to certain concentration properties of the offspring distribution. This allows to derive reconstruction thresholds for a very wide family of offspring distributions, which includes B(n,d/n). A very interesting corollary is that for distributions with expected offspring d, we get reconstruction threshold d/ln(d) under weaker concentration conditions than what we have in B(n,d/n). Furthermore, our reconstruction threshold for the random colorings of Galton-Watson with offspring B(n,d/n), implies the reconstruction threshold for the random colourings of G(n,d/n)

Forwarding and optical indices of 4-regular circulant networks

An all-to-all routing in a graph $G$ is a set of oriented paths of $G$, with exactly one path for each ordered pair of vertices. The load of an edge under an all-to-all routing $R$ is the number of times it is used (in either direction) by paths of $R$, and the maximum load of an edge is denoted by $\pi(G,R)$. The edge-forwarding index $\pi(G)$ is the minimum of $\pi(G,R)$ over all possible all-to-all routings $R$, and the arc-forwarding index $\overrightarrow{\pi}(G)$ is defined similarly by taking direction into consideration, where an arc is an ordered pair of adjacent vertices. Denote by $w(G,R)$ the minimum number of colours required to colour the paths of $R$ such that any two paths having an edge in common receive distinct colours. The optical index $w(G)$ is defined to be the minimum of $w(G,R)$ over all possible $R$, and the directed optical index $\overrightarrow{w}(G)$ is defined similarly by requiring that any two paths having an arc in common receive distinct colours. In this paper we obtain lower and upper bounds on these four invariants for $4$-regular circulant graphs with connection set $\{\pm 1,\pm s\}$, $1<s<n/2$. We give approximation algorithms with performance ratio a small constant for the corresponding forwarding index and routing and wavelength assignment problems for some families of $4$-regular circulant graphs.Comment: 19 pages, no figure in Journal of Discrete Algorithms 201

Directed Ramsey number for trees

In this paper, we study Ramsey-type problems for directed graphs. We first consider the $k$-colour oriented Ramsey number of $H$, denoted by $\overrightarrow{R}(H,k)$, which is the least $n$ for which every $k$-edge-coloured tournament on $n$ vertices contains a monochromatic copy of $H$. We prove that $\overrightarrow{R}(T,k) \le c_k|T|^k$ for any oriented tree $T$. This is a generalisation of a similar result for directed paths by Chv\'atal and by Gy\'arf\'as and Lehel, and answers a question of Yuster. In general, it is tight up to a constant factor. We also consider the $k$-colour directed Ramsey number $\overleftrightarrow{R}(H,k)$ of $H$, which is defined as above, but, instead of colouring tournaments, we colour the complete directed graph of order $n$. Here we show that $\overleftrightarrow{R}(T,k) \le c_k|T|^{k-1}$ for any oriented tree $T$, which is again tight up to a constant factor, and it generalises a result by Williamson and by Gy\'arf\'as and Lehel who determined the $2$-colour directed Ramsey number of directed paths.Comment: 27 pages, 14 figure

Reconstruction of Random Colourings

Reconstruction problems have been studied in a number of contexts including biology, information theory and and statistical physics. We consider the reconstruction problem for random $k$-colourings on the $\Delta$-ary tree for large $k$. Bhatnagar et. al. showed non-reconstruction when $\Delta \leq \frac12 k\log k - o(k\log k)$ and reconstruction when $\Delta \geq k\log k + o(k\log k)$. We tighten this result and show non-reconstruction when $\Delta \leq k[\log k + \log \log k + 1 - \ln 2 -o(1)]$ and reconstruction when $\Delta \geq k[\log k + \log \log k + 1+o(1)]$.Comment: Added references, updated notatio

On the editing distance of graphs

An edge-operation on a graph $G$ is defined to be either the deletion of an existing edge or the addition of a nonexisting edge. Given a family of graphs $\mathcal{G}$, the editing distance from $G$ to $\mathcal{G}$ is the smallest number of edge-operations needed to modify $G$ into a graph from $\mathcal{G}$. In this paper, we fix a graph $H$ and consider ${\rm Forb}(n,H)$, the set of all graphs on $n$ vertices that have no induced copy of $H$. We provide bounds for the maximum over all $n$-vertex graphs $G$ of the editing distance from $G$ to ${\rm Forb}(n,H)$, using an invariant we call the {\it binary chromatic number} of the graph $H$. We give asymptotically tight bounds for that distance when $H$ is self-complementary and exact results for several small graphs $H$