Difference between revisions of "Team:Toronto/Gold Integrated"

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<h1>Safety</h1>
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<h1>HP/Gold</h1>
<p>Safety is the number one priority</p>
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<h2>General Lab Safety</h2>
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<h2>Guide</h2>
  
<p>Before starting the project, our team completed the biosafety and the biosecurity trainings provided by the University of Toronto Biosafety office, and our project supervisor, Dr. Radhakrishnan Mahadevan. The training modules completed include lab access and rules, biosafety levels and equipment, emergency procedures etc.</p>
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<p>Establishing meaningful and informed dialogue with our stakeholders is one of the overarching goals of our human practices. We therefore a video interview series with various scientific and social stakeholders to identify the state of the current research and current ethical shoertcomings. In particular, we found a clear ethical guideline as a key unmet need for shaping future application of our system to human gene editing. Based on key principles put forward by the Committee on Human Gene Editing: Scientific, Medical, and Ethical Considerations in their 2017 report on science, ethics and governance, we developed a guideline for iGEM teams to develop integrative human practices to their project design. We then evaluated our team’s efforts based on those criteria and identified strengths and areas for improvement. In particular, transparency through clear documentation and public engagement, identification of vulnerable groups and collaborations were some of our strengths while due care through the development of scenarios and economic considerations in the distribution of our technology are some areas that were touched upon but could be improved by following the recommendations made in our guide.</p>
<p>Overall, our team adhered to the Canadian Biosafety Standards and Guidelines.<sup><a href="#ref1">[1]</a></sup> The biosafety of our lab was overseen by the University's Institutional Biosafety Committee, with administrative and technical support provided by the Biosafety Team in the Office of Environmental Health and Safety.<sup><a href="#ref2">[2]</a></sup></p>
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<a href='https://2017.igem.org/Team:Toronto/Guide'><button class="btn-primary red">Guide</button></a>
 
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<h2>Hardware</h2>
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<p>Throughout our project, we developed multiple hardware devices in order to assay the biological parts that we created in the lab. As we began to integrate LacILOV into a CRISPR switch and began to conceptualize upon its role in gene editing, we recognized that this application would require a tailored hardware device with unique needs compared to the previous versions employed for our experiments.</p>
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Since we were already engaging with stakeholders as a part of our human practices interview series, we decided to use this opportunity to garner feedback regarding future designs of our hardware. Ultimately, this consultation with our interviewees as well as other individuals experienced with mammalian cell cultures led us to develop v4.0 Lancelot. V4.0 Lancelot is a conceptual design intended to be compatible with gene editing applications in mammalian cells. For more technical information about Lancelot, see <a href='https://2017.igem.org/Team:Toronto/Hardware'>Hardware</a>
<li id="ref1">Canadian Biosafety Standards and Guidelines - <a href="https://www.canada.ca/en/public-health/services/canadian-biosafety-standards-guidelines.html">https://www.canada.ca/en/public-health/services/canadian-biosafety-standards-guidelines.html</a></li>
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Based from the feedback we received, if constructed, v4.0 Lancelot would serve as a valuable device that would aid the transition of LacILOV, and tools such as our switch, into mammalian gene editing applications applications.
<li id="ref2">Biosafety Team in the Office of Environmental Health and Safety - <a href="https://ehs.utoronto.ca/our-services/biosafety/">https://ehs.utoronto.ca/our-services/biosafety/</a></li>
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<li id="ref3">NIH Guidelines - <a href="https://www.canada.ca/en/public-health/services/laboratory-biosafety-biosecurity/pathogen-safety-data-sheets-risk-assessment.html">https://www.canada.ca/en/public-health/services/laboratory-biosafety-biosecurity/pathogen-safety-data-sheets-risk-assessment.html</a></li>
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<a href='https://2017.igem.org/Team:Toronto/Hardware'><button class="btn-primary red">Guide</button></a>
<li id="ref4">iGEM Risk Groups - <a href="https://2017.igem.org/Safety/Risk_Groups">https://2017.igem.org/Safety/Risk_Groups</a></li>
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Revision as of 03:40, 2 November 2017

HP/Gold

Guide

Establishing meaningful and informed dialogue with our stakeholders is one of the overarching goals of our human practices. We therefore a video interview series with various scientific and social stakeholders to identify the state of the current research and current ethical shoertcomings. In particular, we found a clear ethical guideline as a key unmet need for shaping future application of our system to human gene editing. Based on key principles put forward by the Committee on Human Gene Editing: Scientific, Medical, and Ethical Considerations in their 2017 report on science, ethics and governance, we developed a guideline for iGEM teams to develop integrative human practices to their project design. We then evaluated our team’s efforts based on those criteria and identified strengths and areas for improvement. In particular, transparency through clear documentation and public engagement, identification of vulnerable groups and collaborations were some of our strengths while due care through the development of scenarios and economic considerations in the distribution of our technology are some areas that were touched upon but could be improved by following the recommendations made in our guide.

Hardware

Throughout our project, we developed multiple hardware devices in order to assay the biological parts that we created in the lab. As we began to integrate LacILOV into a CRISPR switch and began to conceptualize upon its role in gene editing, we recognized that this application would require a tailored hardware device with unique needs compared to the previous versions employed for our experiments.

Since we were already engaging with stakeholders as a part of our human practices interview series, we decided to use this opportunity to garner feedback regarding future designs of our hardware. Ultimately, this consultation with our interviewees as well as other individuals experienced with mammalian cell cultures led us to develop v4.0 Lancelot. V4.0 Lancelot is a conceptual design intended to be compatible with gene editing applications in mammalian cells. For more technical information about Lancelot, see Hardware Based from the feedback we received, if constructed, v4.0 Lancelot would serve as a valuable device that would aid the transition of LacILOV, and tools such as our switch, into mammalian gene editing applications applications.