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| - | <header1>Chimera
| + | <header1>Chimera</header1><h3>an optimized characterization workflow for synthetic biology</h3> |
| - | </header1>
| + | <maincontent><br> |
| - | <h3>an optimized synthetic biology workflow</h3>
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| | <table width="100%" border="0" cellspacing="0" cellpadding="0"> | | <table width="100%" border="0" cellspacing="0" cellpadding="0"> |
| | <tr> | | <tr> |
| | <td colspan="2" scope="col"> | | <td colspan="2" scope="col"> |
| | <h3>Abstract </h3> | | <h3>Abstract </h3> |
| - | 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 <a href="https://2014.igem.org/Team:BostonU/Workflow">Chimera</a> that will help fellow synthetic biology cloners in the creation of their genetic devices! Chimera utilizes <a href="https://2014.igem.org/Team:BostonU/Software">bio-design automation software tools</a> with experimental protocols and builds upon a thoroughly characterized library of <a href="https://2014.igem.org/Team:BostonU/MoClo">MoClo</a> 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<br> | + | <strong>The Joy of Cloning: Chimera, a Recipe for Integrating Computational Tools with Experimental Protocols </strong><br> |
| - | <li> individual genetic parts (namely tandem promoters, fusion proteins, and different backbones), | + | 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 <a href="https://2014.igem.org/Team:BostonU/Workflow">Chimera</a> that will help fellow synthetic biology cloners in the creation of their genetic devices! Chimera utilizes <a href="https://2014.igem.org/Team:BostonU/Software">bio-design automation software tools</a> with experimental protocols and builds upon a thoroughly characterized library of <a href="https://2014.igem.org/Team:BostonU/MoClo">MoClo</a> 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:<br> |
| - | <li> transcriptional units assembled from individual parts (with both new and previously made MoClo parts), and | + | <p class="tab"><li> individual genetic parts (namely <a href="https://2014.igem.org/Team:BostonU/ProjectTandemPromoters">tandem promoters</a>, <a href="https://2014.igem.org/Team:BostonU/FusionProteins">fusion proteins</a>, and <a href="https://2014.igem.org/Team:BostonU/Backbones">different backbones</a>), </p> |
| - | <li> a complex genetic device (our goal is a <a href="https://2014.igem.org/Team:BostonU/Encoder">priority encoder</a>). | + | <p class="tab"><li> transcriptional units assembled from individual parts (with both new and previously made MoClo parts), and </p> |
| - | <br><br><strong>Click here to explore our project!</strong></td></tr></table> | + | <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> |
| | + | <br><br><strong><a href="https://2014.igem.org/Team:BostonU/Chimera">Click here to explore our project!</a></strong></td></tr></table> |
| | + | </maincontent> |
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| | </div></div> | | </div></div> |
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