Related papers: Chromatic Symmetric Functions of Hypertrees
In the mid-1990s, Stanley and Stembridge conjectured that the chromatic symmetric functions of claw-free co-comparability (also called incomparability) graphs were e-positive. The quest for the proof of this conjecture has led to an…
Fix an integer $k \ge 3$. A $k$-uniform hypergraph is simple if every two edges share at most one vertex. We prove that there is a constant $c$ depending only on $k$ such that every simple $k$-uniform hypergraph $H$ with maximum degree $\D$…
This paper realizes of two families of combinatorial symmetric functions via the complex character theory of the finite general linear group $\mathrm{GL}_{n}(\mathbb{F}_{q})$: chromatic quasisymmetric functions and vertical strip LLT…
An edge-coloring of a connected graph $G$ is called a {\it monochromatic connection coloring} (MC-coloring, for short), introduced by Caro and Yuster, if there is a monochromatic path joining any two vertices of the graph $G$. Let $mc(G)$…
For every positive integer $n$, we construct a Hasse diagram with $n$ vertices and chromatic number $\Omega(n^{1/4})$, which significantly improves on the previously known best constructions of Hasse diagrams having chromatic number…
In this paper, we continue the study of $2$-colorings in hypergraphs. A hypergraph is $2$-colorable if there is a $2$-coloring of the vertices with no monochromatic hyperedge. It is known (see Thomassen [J. Amer. Math. Soc. 5 (1992),…
Let $\Omega_q=\Omega_q(H)$ denote the set of proper $[q]$-colorings of the hypergraph $H$. Let $\Gamma_q$ be the graph with vertex set $\Omega_q$ and an edge ${\sigma,\tau\}$ where $\sigma,\tau$ are colorings iff $h(\sigma,\tau)=1$. Here…
A strong edge colouring of a graph is an assignment of colours to the edges of the graph such that for every colour, the set of edges that are given that colour form an induced matching in the graph. The strong chromatic index of a graph…
A coloring of the vertices of a connected graph is convex if each color class induces a connected subgraph. We address the convex recoloring (CR) problem defined as follows. Given a graph $G$ and a coloring of its vertices, recolor a…
Given a multi-hypergraph $G$ that is edge-colored into color classes $E_1, \ldots, E_n$, a full rainbow matching is a matching of $G$ that contains exactly one edge from each color class $E_i$. One way to guarantee the existence of a full…
We prove that for any tree with a vertex of degree at least six, its chromatic symmetric function is not $e$-positive, that is, it cannot be written as a nonnegative linear combination of elementary symmetric functions. This makes…
The pseudoachromatic index of a graph is the maximum number of colors that can be assigned to its edges, such that each pair of different colors is incident to a common vertex. If for each vertex its incident edges have different color,…
The chromatic polynomial is characterized as the unique polynomial invariant of graphs, compatible with two interacting bialgebras structures: the first coproduct is given by partitions of vertices into two parts, the second one by a…
A hypergraph is "$d$-degenerate" if every subhypergraph has a vertex of degree at most $d$. A greedy algorithm colours every such hypergraph with at most $d+1$ colours. We show that this bound is tight, by constructing an $r$-uniform…
We define a perfect coloring of a graph $G$ as a proper coloring of $G$ such that every connected induced subgraph $H$ of $G$ uses exactly $\omega(H)$ many colors where $\omega(H)$ is the clique number of $H$. A graph is perfectly colorable…
For a hypergraph $H$, let $q(H)$ denote the expected number of monochromatic edges when the color of each vertex in $H$ is sampled uniformly at random from the set of size 2. Let $s_{\min}(H)$ denote the minimum size of an edge in $H$.…
Tree representations of (sets of) symmetric binary relations, or equivalently edge-colored undirected graphs, are of central interest, e.g.\ in phylogenomics. In this context symbolic ultrametrics play a crucial role. Symbolic ultrametrics…
Binary relations derived from labeled rooted trees play an import role in mathematical biology as formal models of evolutionary relationships. The (symmetrized) Fitch relation formalizes xenology as the pairs of genes separated by at least…
This paper investigates methods for calculating the chromatic symmetric function (CSF) of a graph in chromatic-bases and the $m_\lambda$-basis. Our key contributions include a novel approach for calculating the CSF in chromatic-bases…
Let $H=(V(H),E(H))$ be a graph. A $k$-coloring of $H$ is a mapping $\pi : V(H) \longrightarrow \{1,2,\ldots, k\}$ so that each color class induces a $K_2$-free subgraph. For a graph $G$ of order at least $2$, a $G$-free $k$-coloring of $H$…