"
Team:Dundee/Modelling4
From 2012.igem.org
(Difference between revisions)
| Line 69: | Line 69: | ||
<b><h2>Overview</h2></b> | <b><h2>Overview</h2></b> | ||
| - | The problem addressed in this project is characterised by processes occurring over a vast range of spatial and temporal scales: from the protein structure of the type VI secretion system to large-scale effects in the colon. This range of scales presents a chain of biological questions: can we engineer an E.coli that produce enough endolysin to kill C. diff? What are the factors that could lead to success and failure of an E. coli therapy? What if processes are stochastic? Could our engineered E. coli be an efficient solution in realistic conditions? The mathematical modelling component of this project attempts address these questions by both underpinning the lab work and extending it beyond what is capable on the bench. Clicking on the tabs to the right and linking to the Software page, will reveal the variety of modelling techniques used - from ODE and PDE models to our bespoke CellSym cellular automata. Our results obtained so far summarised there. The work continues… | + | The problem addressed in this project is characterised by processes occurring over a vast range of spatial and temporal scales: from the protein structure of the type VI secretion system to large-scale effects in the colon. This range of scales presents a chain of biological questions: can we engineer an E.coli that produce enough endolysin to kill C. diff? What are the factors that could lead to success and failure of an E. coli therapy? What if processes are stochastic? Could our engineered E. coli be an efficient solution in realistic conditions? The mathematical modelling component of this project attempts address these questions by both underpinning the lab work and extending it beyond what is capable on the bench. Clicking on the tabs to the right and linking to the Software page, will reveal the variety of modelling techniques used - from ODE and PDE models to our bespoke CellSym cellular automata. Our results obtained so far summarised there. The work continues…<br><br> |
| - | </div> | + | |
| + | <center> | ||
| + | <img src="https://static.igem.org/mediawiki/2012/a/a9/Mathspic.jpg"> | ||
| + | <center> | ||
| + | |||
| + | |||
| + | </div> | ||
<div class="pickerbox"> | <div class="pickerbox"> | ||
Revision as of 19:59, 23 September 2012
Overview
The problem addressed in this project is characterised by processes occurring over a vast range of spatial and temporal scales: from the protein structure of the type VI secretion system to large-scale effects in the colon. This range of scales presents a chain of biological questions: can we engineer an E.coli that produce enough endolysin to kill C. diff? What are the factors that could lead to success and failure of an E. coli therapy? What if processes are stochastic? Could our engineered E. coli be an efficient solution in realistic conditions? The mathematical modelling component of this project attempts address these questions by both underpinning the lab work and extending it beyond what is capable on the bench. Clicking on the tabs to the right and linking to the Software page, will reveal the variety of modelling techniques used - from ODE and PDE models to our bespoke CellSym cellular automata. Our results obtained so far summarised there. The work continues…
