IGEM
From OpenWetWare
iGEM is the international genetically engineered machines competition. The objective of the competition is to design and build an engineered biological system using DNA. Systems will be constructed from standard biological parts. You can read more about last year's competition here or check out the 2008 wiki. |
See iGEM:Help for useful help pages for iGEM teams! Please add to the list. |
Team pages hosted on OWW
2008
- Brown University
- Caltech
- Harvard
- Johns Hopkins University
- Kyoto University
- Melbourne
- MIT
- Nanyang Technological University
- Newcastle University
- TU Delft
- University of Hawaii
- University of Warsaw
- University of Washington
2007
- Brown University
- Caltech
- Harvard
- Imperial
- MIT
- NYMU
- Peking
- Penn State
- Tianjin University
- Tsinghua
- Turkey
- Virginia
- UCSF
- Davidon/Missouri Western State University
2006
Useful pages for inter-team collaboration
- iGEM:Instructions on starting a lab notebook -- Use OWW's new lab notebook too organize and share your work over the summer.
- IGEM:Idea exchange -- Post ideas your team didn't decide to use, maybe another team has the expertise/interest to pull it off.
- Sidebar:iGEM -- Add to your Sidebar an iGEM related set of links. Add any generally useful links to that page for iGEM.
- Helpful tutorials from John Chris Anderson at berkeley
Wiki tips
- To easily add a link to a part's Registry page, use the
<bbpart></bbpart>
tags. For instance,<bbpart>BBa_R0011</bbpart>
gives <bbpart>BBa_R0011</bbpart>.
History
==IGEM recent changes==
List of abbreviations:
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N 18:40 | 3D Cell Culture - McLean Taggart, Emma Villares, Maximillian Marek, Scott LeBlanc, Adam Lyons and Jacob Belden diffhist +24,060 CarterPaul talk contribs (Created page with "{{Template:CHEM-ENG590E}} ==Introduction== While most microfluidic devices incorporate a 2D cell culture design, in which a single layer of cells is grown on the bottom of a device, these systems suffer from poor <i>in vivo</i> mimicry, as, in the human body, most cells grow in all directions.<sup>https://doi.org/10.5114/aoms.2016.63743 1</sup> To address this limitation, 3D cell culture devices have been developed - in w...") |
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18:36 | 3D Cell Culture - McLean Taggart, Emma Villares, Maximillian Marek, Scott LeBlanc, and Adam Lyons diffhist +5,343 CarterPaul talk contribs (Added a Technique and applications section) |
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10:20 | Yarn Microfluidics - Roger Dirth 12 changes history +442 [Rcostello (12×)] | |||
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08:18 | 3D Printed Microfluidic Robots - Helen Hua 2 changes history +6 [Michele Caggioni (2×)] | |||
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22:11 | The paper that launched microfluidics - Xi Ning 11 changes history +4,793 [Xning098 (11×)] | |||
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