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| - | {{:Team:Paris_Bettencourt/tpl_test}}
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| - | <html>
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| - | <h2>Risc project</h2>
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| - | <p>
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| - | The risc is a long term project. It consist in a Database of pre-constructed pattern describing minimalist biological behaviours.
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| - | <br/>
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| - | So, it introduce the concept of usualy used Biobrick's pattern database based on the frequency of biobrick construct in Igem team.
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| - | The objective is to simplify design of synthetic systems by using intuitive pattern describing the behaviour we need insteed of combining a lot of biobrick.
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| - | It is a way of having an abstraction of the biobrick level. also : for a behaviour, we can find different patterns.
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| - | For example, for an inhibition behaviour, we can use a promoter, a RBS or RNA degradation.
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| - | The idea is having behind this description a compiler working on those behaviour and choosing the finest pattern for the behaviour we are looking for.
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| - | </p>
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| - | <h2>compilation</h2>
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| - | <table>
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| - | <tr>
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| - | <td>
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| - | <p>This project is based on an other project witch consist in using a high level behavious langage for synthetic biology.
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| - | </p>
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| - | </td></tr>
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| - | <tr><td>
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| - | <img src="https://static.igem.org/mediawiki/2011/a/a5/Igemparis2011Compil.png" width="800"/>
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| - | </td></tr>
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| - | <tr><td>
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| - | <p>
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| - | we will use those minimalist patterns by combination and substitution to simulate the model described by the langage.
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| - | </p>
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| - | <table>
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| - | <tr>
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| - | <td align="center"><h3>Combination</h3></td><td align="right"><img src="https://static.igem.org/mediawiki/2011/e/e6/Igemparis2011Combinaison.png"/></td>
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| - | </tr><tr>
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| - | <td align="center"><h3>Substitution</h3></td><td align="right"><img src="https://static.igem.org/mediawiki/2011/7/74/Paris2011Substitution.png"/></td>
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| - | </tr>
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| - | </table>
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| - | </td></tr>
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| - | <tr><td>
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| - | <p>
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| - | Our approach is to propose to creat a comportemental description of those patterns instead of a structural design. This to facilitate the usage of these construct.
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| - | this idea is different from other modeling method by not trying to modelize biologic systems but having the biologic system simulating the model(doing possibly more than the model but not less).
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| - | </p>
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| - | </td></tr>
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| - | <tr><td><p>
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| - | We starded by analysing older igem project looking for common used biobrick circuit and define the behaviour of those circuits.
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| - | </tr></td></p>
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| - | </table>
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| - | <h2>Example of patterns</h2>
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| - | <table border="2px">
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| - | <tr>
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| - | <td><h3>Mechanism</h3></td>
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| - | <td><h3>Pattern description</h3></td>
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| - | <td><h3>Pattern code</h3></td>
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| - | </tr><tr>
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| - | <td>Transposon<img src="https://static.igem.org/mediawiki/2011/2/27/Paris2011Transposon.png" width="200"/></td>
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| - | <td><ul><li>in : one sequence with 2 extraction site</li><li>out : 1 sequence extracted and the original sequence regenerated</li><li>behaviours : extract a part of a sequence and potentialy active another</li></ul></td>
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| - | <td><img src="https://static.igem.org/mediawiki/2011/d/d7/Igem2011Transposoncode.png" width="400"/></td>
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| - | </tr><tr>
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| - | <td>Phage<img src="https://static.igem.org/mediawiki/2011/2/2e/Paris2011Phage.png" width="200"/></td>
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| - | <td><ul><li>in : 1 sequence with 2 insertion site and 1 plasmid with 2 attachment sites</li><li>out : 1 sequence combination of the two first</li><li>behaviours : insert a subsequence in a DNA sequence</li></ul></td>
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| - | <td><img src="https://static.igem.org/mediawiki/2011/c/c0/Paris2011Phagecode.png" width="400"/></td>
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| - | </tr>
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| - | </table>
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