Introduction and Overview
Networks arise in many scientific applications, from resource allocation/transportation problems, to electrical engineering networks, to the study of biochemical reactions systems. While the intended applications and analytic techniques vary significantly in these disciplines, the core goal remains the same: to extract as much information as possible about the dynamical behaviors of the resulting systems from the structure of the network itself.
Organization and Contacts
The Networks Seminar is currently organized by Matthew D. Johnston, David F. Anderson, and Gheorghe Craciun. Contact information, including how to join the mailing list, is contained below:
Matthew D. Johnston
David F. Anderson
Join Mailing List: join-math-networks-seminar[at]lists.wisc.edu
Email Mailing List: networksem[at]math.wisc.edu
The seminar will take place on Wednesdays in 901 Van Vleck Hall at 2:25 PM, unless otherwise noted.
Wednesday, January 28
Wednesday, February 4
Wednesday, February 11
Wednesday, February 18
Wednesday, February 25
Wednesday, September 17, Matthew D. Johnston (UW-Madison)
Title: An Introduction to Chemical Reaction Network Theory
Abstract: There has been significant interest recently in the relationship between the kinetic of models of biochemical reaction networks and the underlying network structure. In this introductory talk, we will discuss the basic features of so-called Chemical Reaction Network Theory which has been an active area of research since the 1970s. In particular, graph-theoretic notions such as weak reversibility and network deficiency will be introduced. We will also discuss reasonable modeling choices---including deterministic and stochastic formulations---and summarize a few surprising results which hold for deterministically modeled mass action systems.
Monday, September 22 (2:25 p.m. in Van Vleck B105) Casian Pantea (WVU)
Title: Injectivity and multistationarity in chemical reaction networks
Abstract: Much attention has been paid recently to bistability and switch-like behavior that might be resident in important biochemical reaction networks. It turns out that large classes of extremely complex networks cannot give rise to multistationarity, no matter what their reaction rates might be. In turn, absence of multistationarity in a reaction network is often a consequence of the corresponding vector field being injective. In this talk I will give an overview of both older and newer injectivity results for vector fields associated with a biochemical reaction network. As much as possible, the matrix-theoretic techniques behind these results will also be discussed.
Wednesday, October 1 David F. Anderson (UW-Madison)
Title: Deficiency and stochastic models of biochemical reaction networks
Abstract: The deficiency of a reaction network is central to many results from chemical reaction network theory. In this talk, I will explain what the deficiency of a reaction network is, and how it can be used to shed light on the behavior of the associated mathematical models. I will try to discuss results for both deterministic and stochastic models.
Wednesday, October 15, Daniele Cappelletti (University of Copenhagen)
Title: Elimination of intermediate species in biochemical reaction networks
Abstract: Biochemical reactions often proceed through the formation of transient intermediate species. These species are usually more unstable than the other species and degraded at a faster rate. Due to the complexity and intractability of many reaction networks, intermediate species are therefore often ignored in the models. In this talk I will formally introduce stochastic reaction networks and unveil a connection with the deterministic ones. Further, I will show an asymptotic result giving some condition on when it is possible to safely ignore intermediate species, both in the stochastic and deterministic frameworks. I will finally show some further issues on intermediate species I am currently working on.
Wednesday, October 22; October 29; November 5, Gheorghe Craciun (UW-Madison)
Title: Persistence properties of mass action systems
Abstract: A positive trajectory of a dynamical system is called persistent if, in the long run, it does not approach the boundary of the positive orthant. In biological applications, the persistence property is critical in deciding if a species in an ecosystem will become extinct, an infection will die off, or a chemical species will be completely consumed by a reaction network. We describe some classes of dynamical systems for which all positive trajectories are persistent. We also describe connections to the Global Attractor Conjecture, which says that a large class of mass-action systems (called complex balanced or toric dynamical systems) have a global attractor within any invariant subspace.
Wednesday, November 19 Matthew D. Johnston (UW-Madison)
Title: Recent Results in Chemical Reaction Network Theory
Abstract: In this talk, I will present some recent results in two related areas of Chemical Reaction Network Theory. (1) I will present a method called network translation which is often capable of determinining characteristics of the steady state sets of deterministically modeled mass action systems. The method associates the original reaction network to a related non-physical network which is more strongly connected than the original one. (2) I will investigate differences in long-term behavior between traditional deterministic models of chemical reaction systems and the more physically realistic stochastic models. I will present a classification of systems for which the deterministic model often predicts positivity, but for which an extinction event necessarily occurs when modeled stochastically.
Friday, December 5 (11:00 a.m. in Van Vleck 901), Nikki Meshkat (NCSU)
Title: Finding identifiable functions of linear and nonlinear biological models
Abstract: Identifiability concerns finding which unknown parameters of a model can be quantified from given input-output data. Many linear ODE models, used primarily in Systems Biology, are unidentifiable, which means that parameters can take on an infinite number of values and yet yield the same input-output data. For a given unidentifiable model, the goal is then to find a set of identifiable functions, i.e. parameter combinations, and then attempt to find a scaling reparametrization so that the resulting model is identifiable. We examine this problem of finding a simple set of identifiable parameter combinations for both linear and nonlinear models. In particular, we use a graph-theoretic approach to find identifiable parameter combinations for linear compartment models and also demonstrate an algorithm using Grobner bases to find identifiable parameter combinations for nonlinear models. We demonstrate these results using our web implementation, COMBOS.