Difference between revisions of "Team:Vanderbilt/Project/Achievements"

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<li>Cloned five exogenous DNA repair enzymes </li>
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<li>Introduced quantitative metric of expected evolutionary stability and computationally modeled simple circuits</li>
<li>Incorporated KIKO vector for genomic integration and simultaneous knock-out</li>
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<li>Invented software tool to analyze circuit designs, calculate stability, and suggest modifications to improvements </li>
<li>Designed “Incorruptible Cell” that commits suicide instead of passing on mutations
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<li>Developed assays for measuring decreased recombination with homology-minimization software</li>
 +
<li>Constructed optimized circuit to demonstrate improved stability with VERT technique</li>
 +
<li>Validated bidirectional promoter for use with system to select against promoter mutation
 
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   <img src="https://static.igem.org/mediawiki/2015/1/14/VU15_circuit_logo.png" width="300px" />
 
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<ul>
 
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<li>Introduced quantitative metric of expected evolutionary stability and computationally modeled simple circuits</li>
+
<li>Cloned five exogenous DNA repair enzymes </li>
<li>Invented software tool to analyze circuit designs, calculate stability, and suggest modifications to improvements </li>
+
<li>Incorporated KIKO vector for genomic integration and simultaneous knock-out</li>
<li>Developed assays for measuring decreased recombination with homology-minimization software</li>
+
<li>Designed “Incorruptible Cell” that commits suicide instead of passing on mutations
<li>Constructed optimized circuit to demonstrate improved stability with VERT technique</li>
+
<li>Validated bidirectional promoter for use with system to select against promoter mutation
+
 
</li></ul>
 
</li></ul>
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Revision as of 06:57, 20 November 2015

Vanderbilt iGEM 2015

Sequence

  • Invented an innovative software tool for minimizing any gene’s susceptibility to mutation
  • Validated rapid spread of mutants in a genetically modified population by mathematical and empirical techniques
  • Experimentally validated decreased mutation in optimized sequences with
    • Multiple mutagen types (UV radiation, oxidation)
    • Multiple quantification protocols (Alkaline gel, plasmid conformation, PCR inhibition)
  • Established high expression of optimized sequences
  • Modeling and computational strategies for further improvements and expansion of software
  • Investigated potential for nanopore sequencing to become next-generation of ultra high-throughput DNA damage detection

Circuit

  • Introduced quantitative metric of expected evolutionary stability and computationally modeled simple circuits
  • Invented software tool to analyze circuit designs, calculate stability, and suggest modifications to improvements
  • Developed assays for measuring decreased recombination with homology-minimization software
  • Constructed optimized circuit to demonstrate improved stability with VERT technique
  • Validated bidirectional promoter for use with system to select against promoter mutation

Organism

  • Cloned five exogenous DNA repair enzymes
  • Incorporated KIKO vector for genomic integration and simultaneous knock-out
  • Designed “Incorruptible Cell” that commits suicide instead of passing on mutations