Team:BostonU

From 2014.igem.org

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<p class="tab"><li> transcriptional units assembled from individual parts (with both new and previously made MoClo parts), and </p>
<p class="tab"><li> transcriptional units assembled from individual parts (with both new and previously made MoClo parts), and </p>
<p class="tab"><li> a complex genetic device (our goal is a <a href="https://2014.igem.org/Team:BostonU/Encoder">priority encoder</a>).</p>
<p class="tab"><li> a complex genetic device (our goal is a <a href="https://2014.igem.org/Team:BostonU/Encoder">priority encoder</a>).</p>
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<br><br><strong><a href="https://2014.igem.org/Team:BostonU/Overview">Click here to explore our project!</a></strong></td></tr></table>
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<br><br><strong><a href="https://2014.igem.org/Team:BostonU/Chimera">Click here to explore our project!</a></strong></td></tr></table>
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Revision as of 23:39, 17 October 2014



Chimera

an optimized synthetic biology workflow

Abstract

If BU can clone it, so can you! With a pinch of wet lab work and a dash of computational tools, we have developed a new recipe called Chimera that will help fellow synthetic biology cloners in the creation of their genetic devices! Chimera utilizes bio-design automation software tools with experimental protocols and builds upon a thoroughly characterized library of MoClo parts. This recipe, or workflow, integrates software tools to reduce human error and to structure the way device designs are chosen, assembled, and tested. To demonstrate that this workflow can be used by any level of cloner (beginner, intermediate, and advanced), we will highlight how we used Chimera to create:

  • individual genetic parts (namely tandem promoters, fusion proteins, and different backbones),

  • transcriptional units assembled from individual parts (with both new and previously made MoClo parts), and

  • a complex genetic device (our goal is a priority encoder).



    Click here to explore our project!


    • Our Sponsors

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