Difference between revisions of "Missouri Western/Davidson iGEM2009"

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<center>'''Biology-based'''</center>
 
<center>'''Biology-based'''</center>
 
#What is msDNA?
 
#What is msDNA?
 
 
#How is msDNA normally produced?
 
#How is msDNA normally produced?
 
 
#How is msDNA stored in E. coli? How many copies are carried per cell?  
 
#How is msDNA stored in E. coli? How many copies are carried per cell?  
 
 
#What is the sequence of bacterial reverse transcriptase and can we clone that gene?
 
#What is the sequence of bacterial reverse transcriptase and can we clone that gene?
 
 
#Can we redesign the normal msDNA pathway to produce new segments of DNA of our choosing?
 
#Can we redesign the normal msDNA pathway to produce new segments of DNA of our choosing?
  
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<center>'''Math-based'''</center>
 
<center>'''Math-based'''</center>
 
#What interesting challenges or problems does origami offer?
 
#What interesting challenges or problems does origami offer?
 
 
#Can we produce a series of increasingly difficult goals that might be possible to produce in the lab?
 
#Can we produce a series of increasingly difficult goals that might be possible to produce in the lab?
 
 
#What has been done before and how can we improve upon that?
 
#What has been done before and how can we improve upon that?
 
 
#We can perform some pilot experiments using synthesized DNA and later switch to msDNA (maybe).
 
#We can perform some pilot experiments using synthesized DNA and later switch to msDNA (maybe).

Revision as of 13:43, 2 April 2009

This space will be used starting April, 2009 for brainstorming and a shared whiteboard space.

We need to learn more about these topics:

Biology-based
  1. What is msDNA?
  2. How is msDNA normally produced?
  3. How is msDNA stored in E. coli? How many copies are carried per cell?
  4. What is the sequence of bacterial reverse transcriptase and can we clone that gene?
  5. Can we redesign the normal msDNA pathway to produce new segments of DNA of our choosing?


Math-based
  1. What interesting challenges or problems does origami offer?
  2. Can we produce a series of increasingly difficult goals that might be possible to produce in the lab?
  3. What has been done before and how can we improve upon that?
  4. We can perform some pilot experiments using synthesized DNA and later switch to msDNA (maybe).