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

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             <a href="#" class="btn btn-default"><img src="https://static.igem.org/mediawiki/2015/e/ef/Vanderbilt_2015_flask_red_unselected.png" alt="project" height="36" width="32"/></a>
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             <a href="https://2015.igem.org/Team:Vanderbilt/Project/Sequence" class="btn btn-default">Sequence</a>

Revision as of 15:42, 19 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

Organism

  • 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

Circuit

  • 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