Related papers: Phase Transitions of the Moran Process and Algorit…

We study the contact process on a class of geometric random graphs with scale-free degree distribution, defined on a Poisson point process on $\mathbb{R}^d$. This class includes the age-dependent random connection model and the soft Boolean…

We show that by restricting the degrees of the vertices of a graph to an arbitrary set \( \Delta \), the threshold point $ \alpha(\Delta) $ of the phase transition for a random graph with $ n $ vertices and $ m = \alpha(\Delta) n $ edges…

A significant generalization of the Erd\"os-R\'enyi random graph model is an `inhomogeneous' random graph where the edge probabilities vary according to vertex types. We identify the threshold value for this random graph with a finite…

We study the stabilization time of a wide class of processes on graphs, in which each node can only switch its state if it is motivated to do so by at least a $\frac{1+\lambda}{2}$ fraction of its neighbors, for some $0 < \lambda < 1$. Two…

We consider a synchronous process of particles moving on the vertices of a graph $G$, introduced by Cooper, McDowell, Radzik, Rivera and Shiraga (2018). Initially, $M$ particles are placed on a vertex of $G$. In subsequent time steps, all…

We consider a system of interacting random walks known as the frog model. Let $\mathcal{K}_n=(\mathcal{V}_n,\mathcal{E}_n)$ be the complete graph with $n$ vertices and $o\in\mathcal{V}_n$ be a special vertex called the root. Initially,…

In this paper, we present two main results. First, by only one conjecture (Conjecture 2.9) for recognizing a vertex symmetric graph, which is the hardest task for our problem, we construct an algorithm for finding an isomorphism between two…

We study the time that the simple exclusion process on the complete graph needs to reach equilibrium in terms of total variation distance. For the graph with n vertices and 1<<k<n/2 particles we show that the mixing time is of order…

Consider a system of $K$ particles moving on the vertex set of a finite connected graph with at most one particle per vertex. If there is one, the particle at $x$ chooses one of the $\hbox{deg} (x)$ neighbors of its location uniformly at…

Graph-limit theory focuses on the convergence of sequences of graphs when the number of nodes becomes arbitrarily large. This framework defines a continuous version of graphs allowing for the study of dynamical systems on very large graphs,…

We present the first algorithm to morph graphs on the torus. Given two isotopic essentially 3-connected embeddings of the same graph on the Euclidean flat torus, where the edges in both drawings are geodesics, our algorithm computes a…

We study one specific version of the contact process on a graph. Here, we allow multiple infections carried by the nodes and include a probability of removing nodes in a graph. The removal probability is purely determined by the number of…

Consider branching Brownian motion in which we begin with one particle at the origin, particles independently move according to Brownian motion, and particles split into two at rate one. It is well-known that the right-most particle at time…

In evolutionary game theory, an important measure of a mutant trait (strategy) is its ability to invade and take over an otherwise-monomorphic population. Typically, one quantifies the success of a mutant strategy via the probability that a…

For a graph $H$ and an $n$-vertex graph $G$, the $H$-bootstrap process on $G$ is the process which starts with $G$ and, at every time step, adds any missing edges on the vertices of $G$ that complete a copy of $H$. This process eventually…

Majority bootstrap percolation is a monotone cellular automata that can be thought of as a model of infection spreading in networks. Starting with an initially infected set, new vertices become infected once more than half of their…

We consider the problem of morphing between contact representations of a plane graph. In an $\mathcal F$-contact representation of a plane graph $G$, vertices are realized by internally disjoint elements from a family $\mathcal F$ of…

We introduce and study the mutating contact process, a variant of the multitype contact process, where one type mutates at a constant rate to the other type. We prove that on $\mathbb{Z}$ a single mutant cannot survive while on…

We consider a Moran model with recombination in a haploid population of size $N$. At each birth event, with probability $1-\rho_N R$ the offspring copies one parent's chromosome, and with probability $\rho_N R$ she inherits a chromosome…

Mendelian randomization (MR) is a natural experimental design based on the random transmission of genes from parents to offspring. However, this inferential basis is typically only implicit or used as an informal justification. As…