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Team:Tsinghua-A/Modeling/GILLESPIE/part3
From 2012.igem.org
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1000 trajectories:</br> | 1000 trajectories:</br> | ||
<img src="https://static.igem.org/mediawiki/2012/7/73/THU-AMGP34.png"/> | <img src="https://static.igem.org/mediawiki/2012/7/73/THU-AMGP34.png"/> | ||
| + | From the result, we can see the process more clearly. From the figure of one trajectory, we can see the inversion is reversible so a gene may reverse a lot when Cre-Loxp exists. And the inversion stops when Cre-Loxp is degraded to zero. From all the figures we can see the randomness decreases when the number of trajectories increases. And finally 50% of the genes become the state we want.</br> | ||
</p> | </p> | ||
Revision as of 05:42, 26 September 2012
Tsinghua-A::Modeling
Simulating every single trajectory
1000 genes which are in state ‘A’ are seen as a whole in the above model. To make the simulation more convincing, we then simulate the trajectory of every single molecule. After that we synthesize all trajectories to get the final result.
Result
The concentration of Cre-Loxp :
Then we use green line to denote the number of genes which are in the original state and red line to denote the number of genes which are in the state after inversion.
1 trajectory:
10 trajectories:
100 trajectories:
1000 trajectories:
From the result, we can see the process more clearly. From the figure of one trajectory, we can see the inversion is reversible so a gene may reverse a lot when Cre-Loxp exists. And the inversion stops when Cre-Loxp is degraded to zero. From all the figures we can see the randomness decreases when the number of trajectories increases. And finally 50% of the genes become the state we want.
