Team:ETH Zurich/Modeling/Overview
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'''Questions:'''<br> | '''Questions:'''<br> | ||
- | * Which are the available cutting patterns? | + | * Which are the available restriction enzymes and cutting patterns? |
- | * How is the distribution of genes in each fragment related to the frequence of cutting? | + | * How is the distribution of the genes in each fragment related to the frequence of cutting? |
- | * Is it possible to identify a restriction enzyme that | + | * Is it possible to identify a restriction enzyme that optimizes the probability of genome reduced but vital strains?<br><br> |
'''Method:'''<br> | '''Method:'''<br> | ||
E.Coli K12 genome and annotation was digested using 713 different restriction enzymes and statistical analysis applied on the fragment pattern. | E.Coli K12 genome and annotation was digested using 713 different restriction enzymes and statistical analysis applied on the fragment pattern. |
Revision as of 15:42, 11 October 2008
Overview on the modelling frameworkThis page is meant to give an introduction to the the overall modelling framework we have constructed in order to asses feasibility analysis, temporal scale details and other parameter estimations that regard our project setup. As introduced in the project overview section, four main components can be identified in the deviced mechanism. Accordingly, we divided the modelling framework in four modules that tackles the relative problematics.
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