Team:Paris/Modeling
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We had different approaches to model the biological system. We found interesting to explain at least two ways that we went throught. It is important to understand that both models aim at different goals in the process of understanding our system. | We had different approaches to model the biological system. We found interesting to explain at least two ways that we went throught. It is important to understand that both models aim at different goals in the process of understanding our system. | ||
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= APE (APE Parameters Estimation) Approach = | = APE (APE Parameters Estimation) Approach = | ||
- | + | The second approach was motivated by our will to characterize our system in the most precise way. Each step is taken into account at a fundamental kinetic processes level or at a more global level by a Hill function which is | |
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- | [[Team:Paris/Modeling/ | + | [[Team:Paris/Modeling/BOB|Read more]] |
* What is at stake here is to determine the real parameters that govern the dynamics of our system. | * What is at stake here is to determine the real parameters that govern the dynamics of our system. | ||
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*** Since the β parameter of the Hill function has a linear influence, it is possible to translate this error directly on the parameter; for example: '''β_err = random('norm',β,err)''' where '''β''' is the estimated value of the parameter and '''err''' is the mean of the normalized standard deviations of the experimental values. | *** Since the β parameter of the Hill function has a linear influence, it is possible to translate this error directly on the parameter; for example: '''β_err = random('norm',β,err)''' where '''β''' is the estimated value of the parameter and '''err''' is the mean of the normalized standard deviations of the experimental values. | ||
*** For each cell in the model, we could use such noised values for Vmax parameter, in order to reproduce randomness estimated in the wet lab. | *** For each cell in the model, we could use such noised values for Vmax parameter, in order to reproduce randomness estimated in the wet lab. | ||
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+ | <center>([[Team:Paris/Modeling/Bibliography|Bibliographic References]] - [[Team:Paris/Modeling/linear_approach|Depreciated BoB page]] - [[Team:Paris/Modeling/hill_approach|Depreciated APE page]] - [[Team:Paris/Modeling/estimation|Depreciated Estimation page]] - [[Team:Paris/Modeling/Roadmap|Depreciated Roadmad page]])</center> |
Revision as of 15:20, 27 August 2008
We had different approaches to model the biological system. We found interesting to explain at least two ways that we went throught. It is important to understand that both models aim at different goals in the process of understanding our system. BOB (Based On Bibliography) ApproachOur first approach is quite rough and simple but effective. The goal here was to guess the behavior of our Bacteri'OClock, considering the overall system. Since it is a preliminary approach, we could not yet fill the model with data from the wet lab. This is why our work is mainly based on a bibliographic work, which allow us to use parameters and datas from scientific articles. The keys points of this approach:
APE (APE Parameters Estimation) ApproachThe second approach was motivated by our will to characterize our system in the most precise way. Each step is taken into account at a fundamental kinetic processes level or at a more global level by a Hill function which is
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