Related papers: Long-range competition on the torus
In the two-type Richardson model on a graph $\mathcal{G}=(\mathcal{V},\mathcal{E})$, each vertex is at a given time in state $0$, $1$ or $2$. A $0$ flips to a $1$ (resp.\ $2$) at rate $\lambda_1$ ($\lambda_2$) times the number of…
We study a natural growth process with competition, which was recently introduced to analyze MDLA, a challenging model for the growth of an aggregate by diffusing particles. The growth process consists of two first-passage percolation…
In the standard SIR model, infected vertices infect their neighbors at rate $\lambda$ independently across each edge. They also recover at rate $\gamma$. In this work we consider the SIR-$\omega$ model where the graph structure itself…
We consider Susceptible-Infected-Recovered (SIR) models on dense dynamic random graphs, in which the joint dynamics of vertices and edges are co-evolutionary, i.e., they influence each other bidirectionally. In particular, edges appear and…
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…
We consider the Williams Bjerknes model, also known as the biased voter model on the $d$-regular tree $\bbT^d$, where $d \geq 3$. Starting from an initial configuration of "healthy" and "infected" vertices, infected vertices infect their…
Human diseases spread over networks of contacts between individuals and a substantial body of recent research has focused on the dynamics of the spreading process. Here we examine a model of two competing diseases spreading over the same…
In majority bootstrap percolation on a graph G, an infection spreads according to the following deterministic rule: if at least half of the neighbours of a vertex v are already infected, then v is also infected, and infected vertices remain…
Consider the process where the $n$ vertices of a square $2$-dimensional torus appear consecutively in a random order. We show that typically the size of the $3$-core of the corresponding induced unit-distance graph transitions from $0$ to…
We study the contact process on the complete graph on $n$ vertices where the rate at which the infection travels along the edge connecting vertices $i$ and $j$ is equal to $ \lambda w_i w_j / n$ for some $\lambda >0$, where $w_i$ are i.i.d.…
We study the spread of multi-competitive viruses over a (possibly) time-varying network of individuals accounting for the presence of shared infrastructure networks that further enables transmission of the virus. We establish a sufficient…
The two-type Richardson model describes the growth of two competing infection types on the two or higher dimensional integer lattice. For types that spread with the same intensity, it is known that there is a positive probability for…
In this paper we are concerned with the Susceptible-Infective-Removed model with random transition rates on complete graphs $C_n$ with $n$ vertices. We assign i. i. d. copies of a positive random variable $\xi$ on each vertex as the…
RNA viruses exist in large intra-host populations which display great genotypic and phenotypic diversity. We analyze a model of viral competition between two different viral strains infecting a constantly replenished cell pool, in which we…
We consider the contact process with infection rate $\lambda$ on a random $(d+1)$-regular graph with $n$ vertices, $G_n$. We study the extinction time $\tau_{G_n}$ (that is, the random amount of time until the infection disappears) as $n$…
We consider two competing first passage percolation processes started from uniformly chosen subsets of a random regular graph on $N$ vertices. The processes are allowed to spread with different rates, start from vertex subsets of different…
We study degree-penalized contact processes on Galton-Watson trees (GW) and the configuration model. The model we consider is a modification of the usual contact process on a graph. In particular, each vertex can be either infected or…
We study the early stages of viral infection, and the distribution of times to obtain a persistent infection. The virus population proliferates by entering and reproducing inside a target cell until a sufficient number of new virus…
We introduce a two-type first passage percolation competition model on infinite connected graphs as follows. Type 1 spreads through the edges of the graph at rate 1 from a single distinguished site, while all other sites are initially…
This study extends the SIS epidemic model for single virus propagation over an arbitrary graph to an SI1SI2S epidemic model of two exclusive, competitive viruses over a two-layer network with generic structure, where network layers…