| || || || || || ||1|
|30|| || || || || || ||
Search the School of Mathematical Sciences
People matching "+Mathematical +biology"
Courses matching "+Mathematical +biology"
Mathematical Biology III
The application of mathematics to problems arising in the life sciences is a rapidly growing area yielding quantitative understanding of questions about such things as the spread of infectious diseases, population growth and interaction, organ (e.g. heart) function, cell signalling, nutrient supply, and more. This course will introduce students to the fascinating world of modelling biological systems. A variety of biological problems will be considered, in the context of which students will be exposed to a variety of mathematical techniques. No previous exposure to biology is necessary. Topics covered are: Scalar, discrete-time models, analysed using the mathematical tools of cobwebbing and linear stability analysis of fixed points; Linear stability analysis of systems of discrete-time equations; The theory of dynamical systems for models comprised of linear and nonlinear scalar and coupled ordinary differential equations, including vector fields, phase-plane analysis and elementary bifurcation theory; Reaction-advection-diffusion models, including equation derivation from the law of mass conservation and Fick's law. The 1D Fisher equation is examined in particular, a Hamiltonian function is introduced for analysis of the steady equation, while travelling wave solutions of the unsteady equation are obtained.
More about this course...
Events matching "+Mathematical +biology"
Watching evolution in real time; problems and potential research areas.
15:10 Fri 26 May, 2006 :: G08. Mathematics Building University of Adelaide :: Prof Alan Cooper (Federation Fellow)
Recent studies (1) have indicated problems with our
ability to use the genetic distances between species to estimate the
time since their divergence (so called molecular clocks). An
exponential decay curve has been detected in comparisons of closely
related taxa in mammal and bird groups, and rough approximations
suggest that molecular clock calculations may be problematic for the
recent past (eg <1 million years). Unfortunately, this period
encompasses a number of key evolutionary events where estimates of
timing are critical such as modern human evolutionary history, the
domestication of animals and plants, and most issues involved in
conservation biology. A solution (formulated at UA) will be briefly
outlined. A second area of active interest is the recent suggestion
(2) that mitochondrial DNA diversity does not track population size in
several groups, in contrast to standard thinking. This finding has
been interpreted as showing that mtDNA may not be evolving neutrally,
as has long been assumed.
Large ancient DNA datasets provide a means to examine these issues, by
revealing evolutionary processes in real time (3). The data also
provide a rich area for mathematical investigation as temporal
information provides information about several parameters that are
unknown in serial coalescent calculations (4).References:
- Ho SYW et al. Time dependency of molecular rate estimates and
systematic overestimation of recent divergence
times. Mol. Biol. Evol. 22, 1561-1568 (2005);
Penny D, Nature 436, 183-184 (2005).
- Bazin E., et al. Population size does not influence mitochondrial
genetic diversity in animals. Science 312, 570 (2006);
Eyre-Walker A. Size does not matter for mitochondrial DNA,
Science 312, 537 (2006).
- Shapiro B, et al. Rise and fall of the Beringian steppe
bison. Science 306: 1561-1565 (2004);
Chan et al. Bayesian estimation of the timing and severity of a
population bottleneck from ancient DNA. PLoS Genetics, 2 e59
- Drummond et al. Measurably evolving populations, Trends in
Ecol. Evol. 18, 481-488 (2003);
Drummond et al. Bayesian coalescent inference of past population
dynamics from molecular sequences. Molecular Biology Evolution
22, 1185-92 (2005).
Multi-scale tools for interpreting cell biology data 15:10 Fri 17 Apr, 2009 :: Napier LG29 :: Dr Matthew Simpson :: University of Melbourne
Trajectory data from observations of a random walk process are often used to characterize macroscopic transport coefficients and to infer motility mechanisms in cell biology. New continuum equations describing the average moments of the position of an individual agent in a population of interacting agents are derived and validated. Unlike standard noninteracting random walks, the new moment equations explicitly represent the interactions between agents as they are coupled to the macroscopic agent density. Key issues associated with the validity of the new continuum equations and the interpretation of experimental data will be explored.
Dispersing and settling populations in biology 15:10 Tue 23 Jun, 2009 :: Napier G03 :: Prof Kerry Landman :: University of Melbourne
Partial differential equations are used to model populations (such as cells, animals or molecules) consisting of individuals that undergo two important processes: dispersal and settling. I will describe some general characteristics of these systems, as well as some of our recent projects.
Mathematica Seminar 15:10 Wed 28 Jul, 2010 :: Engineering Annex 314 :: Kim Schriefer :: Wolfram Research
The Mathematica Seminars 2010 offer an opportunity to experience the applicability, ease-of-use, as well as the advancements of Mathematica 7 in education and academic research. These seminars will highlight the latest directions in technical computing with Mathematica, and the impact this technology has across a wide range of academic fields, from maths, physics and biology to finance, economics and business.
Those not yet familiar with Mathematica will gain an overview of the system and discover the breadth of applications it can address, while experts will get firsthand experience with recent advances in Mathematica like parallel computing, digital image processing, point-and-click palettes, built-in curated data, as well as courseware examples.
Why is a pure mathematician working in biology? 15:10 Fri 15 Apr, 2011 :: Mawson Lab G19 lecture theatre :: Associate Prof Andrew Francis :: University of Western Sydney
A pure mathematician working in biology should be a contradiction in
terms. In this talk I will describe how I became interested in working in
biology, coming from an algebraic background. I will also describe some
areas of evolutionary biology that may benefit from an algebraic approach.
Finally, if time permits I will reflect on the sometimes difficult
distinction between pure and applied mathematics, and perhaps venture some
thoughts on mathematical research in general.
Multiscale models of collective cell behaviour: Linear or nonlinear diffusion? 15:10 Fri 4 May, 2012 :: B.21 Ingkarni Wardli :: Dr Matthew Simpson :: Queensland University of Technology
Continuum diffusion models are often used to represent the collective motion of cell populations. Most previous studies have simply used linear diffusion to represent collective cell spreading, while others found that degenerate nonlinear diffusion provides a better match to experimental cell density profiles. There is no guidance available in the mathematical biology literature with regard to which approach is more appropriate. Furthermore, there is no knowledge of particular experimental measurements that can be made to distinguish between situations where these two models are appropriate. We provide a link between individual-based and continuum models using a multiscale approach in which we analyse the collective motion of a population of interacting agents in a generalized lattice-based exclusion process. For round agents that occupy a single lattice site, we find that the relevant continuum description is a linear diffusion equation, whereas for elongated rod-shaped agents that occupy L adjacent lattice sites we find that the relevant continuum description is a nonlinear diffusion equation related to the porous media equation. We show that there are several reasonable approaches for dealing with agent size effects, and that these different approaches are related mathematically through the concept of mean action time. We extend our results to consider proliferation and travelling waves where greater care must be taken to ensure that the continuum model replicates the discrete process. This is joint work with Dr Ruth Baker (Oxford) and Dr Scott McCue (QUT).
Infectious diseases modelling: from biology to public health policy 15:10 Fri 24 Aug, 2012 :: B.20 Ingkarni Wardli :: Dr James McCaw :: The University of Melbourne
The mathematical study of human-to-human transmissible pathogens has
established itself as a complementary methodology to the traditional
epidemiological approach. The classic susceptible--infectious--recovered
model paradigm has been used to great effect to gain insight into the
epidemiology of endemic diseases such as influenza and pertussis, and
the emergence of novel pathogens such as SARS and pandemic influenza.
The modelling paradigm has also been taken within the host and used to
explain the within-host dynamics of viral (or bacterial or parasite)
infections, with implications for our understanding of infection,
emergence of drug resistance and optimal drug-interventions.
In this presentation I will provide an overview of the mathematical
paradigm used to investigate both biological and epidemiological
infectious diseases systems, drawing on case studies from influenza,
malaria and pertussis research. I will conclude with a summary of how
infectious diseases modelling has assisted the Australian government in
developing its pandemic preparedness and response strategies.
How fast? Bounding the mixing time of combinatorial Markov chains 15:10 Fri 22 Mar, 2013 :: B.18 Ingkarni Wardli :: Dr Catherine Greenhill :: University of New South Wales
A Markov chain is a stochastic process which is "memoryless",
in that the next state of the chain depends only on the current state,
and not on how it got there. It is a classical result that an ergodic
Markov chain has a unique stationary distribution.
However, classical theory does not provide any information on the rate of
convergence to stationarity. Around 30 years ago, the mixing time of
a Markov chain was introduced to measure the number of steps required
before the distribution of the chain is within some small distance of
the stationary distribution. One reason why this is important is that
researchers in areas such as physics and biology use Markov chains to
sample from large sets of interest. Rigorous bounds on the mixing time
of their chain allows these researchers to have confidence in their results.
Bounding the mixing time of combinatorial Markov chains can be a challenge, and there are only a few approaches available. I will discuss the main methods and give examples for each (with pretty pictures).
Network-based approaches to classification and biomarker identification in metastatic melanoma 15:10 Fri 2 May, 2014 :: B.21 Ingkarni Wardli :: Associate Professor Jean Yee Hwa Yang :: The University of Sydney
Finding prognostic markers has been a central question in much of current research in medicine and biology. In the last decade, approaches to prognostic prediction within a genomics setting are primarily based on changes in individual genes / protein. Very recently, however, network based approaches to prognostic prediction have begun to emerge which utilize interaction information between genes. This is based on the believe that large-scale molecular interaction networks are dynamic in nature and changes in these networks, rather than changes in individual genes/proteins, are often drivers of complex diseases such as cancer.
In this talk, I use data from stage III melanoma patients provided by Prof. Mann from Melanoma Institute of Australia to discuss how network information can be utilize in the analysis of gene expression analysis to aid in biological interpretation. Here, we explore a number of novel and previously published network-based prediction methods, which we will then compare to the common single-gene and gene-set methods with the aim of identifying more biologically interpretable biomarkers in the form of networks.
Multi-scale modeling in biofluids and particle aggregation 15:10 Fri 17 Jun, 2016 :: B17 Ingkarni Wardli :: Dr Sarthok Sircar :: University of Adelaide
In today's seminar I will give 2 examples in mathematical biology which describes the multi-scale organization at 2 levels: the meso/micro level and the continuum/macro level. I will then detail suitable tools in statistical mechanics to link these different scales.
The first problem arises in mathematical physiology: swelling-de-swelling mechanism of mucus, an ionic gel. Mucus is packaged inside cells at high concentration (volume fraction) and when released into the extracellular environment, it expands in volume by two orders of magnitude in a matter of seconds. This rapid expansion is due to the rapid exchange of calcium and sodium that changes the cross-linked structure of the mucus polymers, thereby causing it to swell. Modeling this problem involves a two-phase, polymer/solvent mixture theory (in the continuum level description), together with the chemistry of the polymer, its nearest neighbor interaction and its binding with the dissolved ionic species (in the micro-scale description). The problem is posed as a free-boundary problem, with the boundary conditions derived from a combination of variational principle and perturbation analysis. The dynamics of neutral gels and the equilibrium-states of the ionic gels are analyzed.
In the second example, we numerically study the adhesion fragmentation dynamics of rigid, round particles clusters subject to a homogeneous shear flow. In the macro level we describe the dynamics of the number density of these cluster. The description in the micro-scale includes (a) binding/unbinding of the bonds attached on the particle surface, (b) bond torsion, (c) surface potential due to ionic medium, and (d) flow hydrodynamics due to shear flow.
On the Willmore energy 15:10 Fri 7 Oct, 2016 :: Napier G03 :: Dr Yann Bernard :: Monash University
The Willmore energy of a surface captures its bending. Originally discovered 200 years ago by Sophie Germain in the context of elasticity theory, it has since then been rediscovered numerous times in several areas of science: general relativity, optics, string theory, conformal geometry, and cell biology. For example, our red blood cells assume a peculiar shape that minimises the Willmore energy.
In this talk, I will present the thrilling history of the Willmore energy, its applications, and its main properties. The presentation will be accessible to all mathematicians as well as to advanced undergraduate students.
Mathematics is Biology's Next Microscope (Only Better!) 15:10 Fri 11 Aug, 2017 :: Ingkarni Wardli B17 :: Dr Robyn Araujo :: Queensland University of Technology
While mathematics has long been considered "an essential tool for physics", the foundations of biology and the life sciences have received significantly less influence from mathematical ideas and theory. In this talk, I will give a brief discussion of my recent research on robustness in molecular signalling networks, as an example of a complex biological question that calls for a mathematical answer. In particular, it has been a long-standing mystery how the extraordinarily complex communication networks inside living cells, comprising thousands of different interacting molecules, are able to function robustly since complexity is generally associated with fragility. Mathematics has now suggested a resolution to this paradox through the discovery that robust adaptive signalling networks must be constructed from a just small number of well-defined universal modules (or "motifs"), connected together. The existence of these newly-discovered modules has important implications for evolutionary biology, embryology and development, cancer research, and drug development.
Mathematics is Biology'ÂÂs Next Microscope (Only Better!) 15:10 Fri 11 Aug, 2017 :: Ingkarni Wardli B17 :: Dr Robyn Araujo :: Queensland University of Technology
While mathematics has long been considered Ã¢ÂÂan essential tool for physics", the foundations of biology and the life sciences have received significantly less influence from mathematical ideas and theory. In this talk, I will give a brief discussion of my recent research on robustness in molecular signalling networks, as an example of a complex biological question that calls for a mathematical answer. In particular, it has been a long-standing mystery how the extraordinarily complex communication networks inside living cells, comprising thousands of different interacting molecules, are able to function robustly since complexity is generally associated with fragility. Mathematics has now suggested a resolution to this paradox through the discovery that robust adaptive signalling networks must be constructed from a just small number of well-defined universal modules (or Ã¢ÂÂmotifsÃ¢ÂÂ), connected together. The existence of these newly-discovered modules has important implications for evolutionary biology, embryology and development, cancer research, and drug development.
How oligomerisation impacts steady state gradient in a morphogen-receptor system 15:10 Fri 20 Oct, 2017 :: Ingkarni Wardli 5.57 :: Mr Phillip Brown :: University of Adelaide
In developmental biology an important process is cell fate determination, where cells start to differentiate their form and function. This is an element of the broader concept of morphogenesis. It has long been held that cell differentiation can occur by a chemical signal providing positional information to 'undecided' cells. This chemical produces a gradient of concentration that indicates to a cell what path it should develop along. More recently it has been shown that in a particular system of this type, the chemical (protein) does not exist purely as individual molecules, but can exist in multi-protein complexes known as oligomers.
Mathematical modelling has been performed on systems of oligomers to determine if this concept can produce useful gradients of concentration. However, there are wide range of possibilities when it comes to how oligomer systems can be modelled and most of them have not been explored.
In this talk I will introduce a new monomer system and analyse it, before extending this model to include oligomers. A number of oligomer models are proposed based on the assumption that proteins are only produced in their oligomer form and can only break apart once they have left the producing cell. It will be shown that when oligomers are present under these conditions, but only monomers are permitted to bind with receptors, then the system can produce robust, biologically useful gradients for a significantly larger range of model parameters (for instance, degradation, production and binding rates) compared to the monomer system. We will also show that when oligomers are permitted to bind with receptors there is negligible difference compared to the monomer system.
The Markovian binary tree applied to demography and conservation biology 15:10 Fri 27 Oct, 2017 :: Ingkarni Wardli B17 :: Dr Sophie Hautphenne :: University of Melbourne
Markovian binary trees form a general and tractable class of continuous-time branching processes, which makes them well-suited for real-world applications. Thanks to their appealing probabilistic and computational features, these processes have proven to be an excellent modelling tool for applications in population biology. Typical performance measures of these models include the extinction probability of a population, the distribution of the population size at a given time, the total progeny size until extinction, and the asymptotic population composition. Besides giving an overview of the main performance measures and the techniques involved to compute them, we discuss recently developed statistical methods to estimate the model parameters, depending on the accuracy of the available data. We illustrate our results in human demography and in conservation biology.
News matching "+Mathematical +biology"
Welcome to Dr Joshua Ross We welcome Dr Joshua Ross as a new lecturer in the School of Mathematical Sciences. Joshua has moved over to Adelaide from the University of Cambridge. His research interests are mathematical modelling (especially mathematical biology) and operations research. Posted Mon 15 Mar 10.
A/Prof Joshua Ross, 2017 Moran Medal recipient Congratulations to Associate Professor Joshua Ross who has won the 2017 Moran Medal, awarded by the Australian Academy of Science.
The Moran Medal recognises outstanding research by scientists up to 10 years post-PhD in applied probability, biometrics, mathematical genetics, psychometrics and statistics.
Associate Professor Ross has made influential contributions to public health and conservation biology using mathematical modelling and statistics to help in decision making.
Posted Fri 23 Dec 16.
Publications matching "+Mathematical +biology"
|Deterministic and stochastic modelling of endosome escape by Staphylococcus aureus: "quorum" sensing by a single bacterium|
Koerber, Adrian; King, J; Williams, P, Journal of Mathematical Biology 50 (440–488) 2005
|Cell-signalling repression in bacterial quorum sensing|
Ward, J; King, J; Koerber, Adrian; Croft, J; Sockett, R; Williams, P, Mathematical Medicine and Biology (Print Edition) 21 (169–204) 2004
|Early development and quorum sensing in bacterial biofilms|
Ward, J; King, J; Koerber, Adrian; Croft, J; Sockett, R; Williams, P, Journal of Mathematical Biology 47 (23–55) 2003
|Modelling host tissue degradation by extracellular bacterial pathogens|
King, J; Koerber, Adrian; Croft, J; Ward, J; Williams, P; Sockett, R, Mathematical Medicine and Biology (Print Edition) 20 (227–260) 2003
|A mathematical model of partial-thickness burn-wound infection by Pseudomonas aeruginosa: Quorum sensing and the build-up to invasion|
Koerber, Adrian; King, J; Ward, J; Williams, P; Croft, J; Sockett, R, Bulletin of Mathematical Biology 64 (239–259) 2002
|Mathematical modelling of quorum sensing in bacteria|
Ward, J; King, J; Koerber, Adrian; Williams, P; Croft, J; Sockett, R, Mathematical Medicine and Biology (Print Edition) 18 (263–292) 2001
Advanced search options
You may be able to improve your search results by using the following syntax:
|Query||Matches the following|
|Asymptotic Equation||Anything with "Asymptotic" or "Equation".
|+Asymptotic +Equation||Anything with "Asymptotic" and "Equation".
|+Stokes -"Navier-Stokes"||Anything containing "Stokes" but not "Navier-Stokes".
|Dynam*||Anything containing "Dynamic", "Dynamical", "Dynamicist" etc.