Biomod/2012/Harvard/BioDesign/approaches: Difference between revisions
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[[Biomod/2012/Harvard/BioDesign/small_canvas_SST |a small SST canvas]], | [[Biomod/2012/Harvard/BioDesign/small_canvas_SST |a small SST canvas]], | ||
[[Biomod/2012/Harvard/BioDesign/large_canvas_SST |a large SST canvas]], | [[Biomod/2012/Harvard/BioDesign/large_canvas_SST |a large SST canvas]], | ||
and [[Biomod/2012/Harvard/BioDesign/DNA_origami |a | and [[Biomod/2012/Harvard/BioDesign/DNA_origami |a 3D DNA origami structure]]. | ||
Second, we optimized the nucleotide sequence of the [[Biomod/2012/Harvard/BioDesign/L-DNA_layer |L-DNA layer]] for infinite tiling and a low melting temperature. | Second, we optimized the nucleotide sequence of the [[Biomod/2012/Harvard/BioDesign/L-DNA_layer |L-DNA layer]] for infinite tiling and a low melting temperature. | ||
Revision as of 22:53, 26 October 2012
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Approaches
Our project had multiple parallel pathways. There were two sub-problems to solve in approaching the templating problem.
One was the templating technique, for which we experimented with three different D-DNA designs;
a small SST canvas, a large SST canvas, and a 3D DNA origami structure.
Second, we optimized the nucleotide sequence of the L-DNA layer for infinite tiling and a low melting temperature.
