Related papers: Phase transitions for contact processes on sparse …
We show that the contact process on the rank-one inhomogeneous random graphs and Erdos-R{\'e}nyi graphs with mean degree large enough survives a time exponential in the size of these graphs for any positive infection rate. In addition, a…
The contact process with an asymptomatic state, introduced in [Belhadji, Lanchier and Mercer, Stochastic Process. Appl., 176:104417, 2024], is a natural variant of the basic contact process that distinguishes between asymptomatic (state 1)…
We consider a continuous-time stochastic model of spiking neurons. In this model, we have a finite or countable number of neurons which are vertices in some graph $G$ where the edges indicate the synaptic connection between them. We focus…
We consider the limiting behavior of the count of subgraphs isomorphic to a graph $G$ with $m\geq 0$ fixed endpoints (or roots) in the random-connection model, as the intensity $\lambda$ of the underlying Poisson point process tends to…
We present general results for the contact process by a method which applies to all transitive graphs of bounded degree, including graphs of exponential growth. The model's infection rates are varied through a control parameter, for which…
To study later spatial evolutionary games based on the multitype contact process, we first focus in this paper on the conditions for survival/extinction in the presence of only one strategy, in which case our model consists of a variant of…
We study the asymptotic spectral behavior of high-dimensional random Gram matrices with sparsity and a variance profile, motivated by applications in wireless communications. Specifically, we consider the Gram matrices $\mathbf S_n=\mathbf…
We consider the contact process on a random graph with fixed degree distribution given by a power law. We follow the work of Chatterjee and Durrett, who showed that for arbitrarily small infection parameter $\lambda$, the survival time of…
We study the contact process on random graphs with low infection rate $\lambda$. For random $d$-regular graphs, it is known that the survival time is $O(\log n)$ below the critical $\lambda_c$. By contrast, on the Erd\H{o}s-R\'enyi random…
The presence of one or more species at some spatial locations but not others is a central matter in ecology. This phenomenon is related to ecological pattern formation. Nonlocal interactions can be considered as one of the mechanisms…
We study the two-species symbiotic contact process (2SCP), recently proposed in [de Oliveira, Santos and Dickman, Phys. Rev. E {\bf 86}, 011121 (2012)] . In this model, each site of a lattice may be vacant or host single individuals of…
We consider the statistical inference problem of recovering an unknown perfect matching, hidden in a weighted random graph, by exploiting the information arising from the use of two different distributions for the weights on the edges…
A superprocess limit for an interacting birth-death particle system modelling a population with trait and physical age-structures is established. Traits of newborn offspring are inherited from the parents except when mutations occur, while…
In a recent paper, Caron and Fox suggest a probabilistic model for sparse graphs which are exchangeable when associating each vertex with a time parameter in $\mathbb{R}_+$. Here we show that by generalizing the classical definition of…
It is known that the limiting behavior of the contact process strongly depends upon the geometry of the graph on which particles evolve: while the contact process on the regular lattice exhibits only two phases, the process on homogeneous…
We classify the possible behaviors of a class of one-dimensional stochastic recurrent growth models. In our main result, we obtain nearly optimal bounds for the tail of hitting times of some compact sets. If the process is an aperiodic…
We present simulation results for the contact process on regular, cubic networks that are composed of a one-dimensional lattice and a set of long edges with unbounded length. Networks with different sets of long edges are considered, that…
We prove a scaling limit theorem for two-type Galton-Waston branching processes with interaction. The limit theorem gives rise to a class of mixed state branching processes with interaction using to simulate the evolution for cell division…
We consider a null-recurrent randomly biased walk $\mathbb{X}$ on a Galton-Watson tree in the (sub)-diffusive regime and we prove that properly renormalized, the local time in a critical generation converges in law towards some function of…
Extinction of a long-lived isolated stochastic population can be described as an exponentially slow decay of quasi-stationary probability distribution of the population size. We address extinction of a population in a two-population system…