Team:EPF Lausanne/Judging

EPFL 2015 iGEM bioLogic Logic Orthogonal gRNA Implemented Circuits EPFL 2015 iGEM bioLogic Logic Orthogonal gRNA Implemented Circuits

Judging

Take a look at our judging form for more details!

Medal criteria

Bronze medal

Criterion Description Link
Register for iGEM, have a great summer, and attend the Giant Jamboree. The team from EPFL (Ecole Polythencique Fédérale de Lausanne) is successful registered for iGEM, the student competition in Synthetic Biology. EPF_Lausanne
Complete judging form The judging form helps iGEM judges to find important informations in order to equally evaluate each team. Judging form
Create and share a Description of the team's project using the iGEM wiki. All the work done by the EPFL iGEM team is documented in this website, called Wiki because powered by Mediawiki. Have a look! Wiki
Present a poster and a talk at the iGEM Jamboree. EPFL iGEM team will fly in Boston on Septenber 24 in order to present the project to other teams coming from all around the world and to discuss it with the judges.
Create a page on your team wiki with clear attribution of each aspect of your project. An iGEM team is often composed of several students with different backgrounds and they are helped by PhD students or professors. The work is attributed clearly to each person which contributed to the project. Attributions
Document at least one new standard BioBrick Part or Device central to your project and submit this part to the iGEM Registry For S. cerevisiae we created new BioBricks. They consists on dCas9 fused with the VP64 RNA polymerase subunit and different synthetic gRNAs. BBa_K1723021
BBa_K1723009
BBa_K1723010
BBa_K1723011
BBa_K1723012
BBa_K1723013
BBa_K1723014
BBa_K1723015
BBa_K1723016
BBa_K1723017
BBa_K1723018
BBa_K1723019
BBa_K1723020

Silver medal

Criterion Description Link
Experimentally validate that at least one new BioBrick Part or Device of your own design and construction works as expected. For E. coli we created new BioBricks and we were able to test them experimentally (cf. our Results page). As for S. cerevisiae these new BioBricks consists on dCas9 fused with a RNA polymerase subunit and synthetic gRNAs. In addition we biobriked a promoter from Bikard et al. and a new entirely synthetic version of it containing others gRNA targeted sites. BBa_K1723000
BBa_K1723005
BBa_K1723002
BBa_K1723003
BBa_K1723004
BBa_K1723006
BBa_K1723007
BBa_K1723008
Submit this new part to the iGEM Parts Registry. All the parts created and experimentally validated in E. coli are submitted to the iGEM Parts Registry. Note that also S. cerevisiae BioBricks (presented as a Bronze Medal requirement) are submitted to the iGEM Parts Registry. BBa_K1723000
BBa_K1723005
BBa_K1723002
BBa_K1723003
BBa_K1723004
BBa_K1723006
BBa_K1723007
BBa_K1723008
iGEM projects involve important questions beyond the bench. Demonstrate how your team has identified, investigated and addressed one or more of these questions in the context of your project. New genome editing and regulation techniques such as CRISPR-Cas9 and dCas have reopened one of the most fundamental debates in synthetic biology: “until where are we allowed to edit genomes, ours included?” thus generating an important media hype. We interested ourselves in how the general public perceives the information coming from the scientific world by organizing a survey in the streets of Lausanne. We also organized a day of activities going from the lab to ethics debates for highschool students. Practices

Gold medal

Criterion Description Link
Expand on your silver medal Human Practices activity or demonstrate an innovative Human Practices activity that relates to your project. In the shadows of the debate raging around new genome editing and regulation techniques such as CRISPR-Cas9 and dCas9, we decided to discuss the data from our public survey with a panel of eleven experts in science, ethics, politics, journalism, industry and religion. We investigated the matters of communication, interaction and responsibility in scientific research in Switzerland and then analyzed and synthesized the views of the experts in a long article. Practices
Improve the function or characterization of a previously existing BioBrick Part or Device Bikard et al. used dCas9-\(\omega\) in order to regulate gene expression. Their dCas9 system works with tracRNAs, while our system works with simpler gRNAs. We also added to the iGEM Parts Registry Bikard's promoter, which is an improved version of the J23117 (BBa_J23117). In addition, to test new gRNA sequences we created a fully synthetic modified version of this promoter. BBa_K1723000
BBa_K1723001
BBa_K1723005
Demonstrate a functional prototype of your project. Design
EPFL 2015 iGEM bioLogic Logic Orthogonal gRNA Implemented Circuits

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