Team:Washington/Outreach/iGEM Collaborations

From 2011.igem.org

(Difference between revisions)
(Implemented Bug Fixes & Features)
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[[File:Washington_collab_test.png|left|550px|thumb|An example of the output from the tool based off of input from our luxC biobrick, multiple primers with various melting temperatures are given]]
[[File:Washington_collab_test.png|left|550px|thumb|An example of the output from the tool based off of input from our luxC biobrick, multiple primers with various melting temperatures are given]]
==Implemented Bug Fixes & Features==
==Implemented Bug Fixes & Features==
-
# Added cyanobacteria to available genomes
+
#Added cyanobacteria to available genomes
#Switch coding sequences in the primer designer to allow for the user to incude a stop codon in a coding sequence. Before, software insisted that coding sequences not include the stop codon
#Switch coding sequences in the primer designer to allow for the user to incude a stop codon in a coding sequence. Before, software insisted that coding sequences not include the stop codon
#Made primer designer default to only check for biobrick restriction enzymes. Before, Primer Designer defaulted to checking  for all restriction sites, making the user scroll to the bottom of the page for results
#Made primer designer default to only check for biobrick restriction enzymes. Before, Primer Designer defaulted to checking  for all restriction sites, making the user scroll to the bottom of the page for results
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[[File:Washington_OldPrimerDesignerdefault.png|left|550px|thumb|Old Default  Primer Designer Output]]
 
#added support for FASTA files with headers
#added support for FASTA files with headers
#added desriptions for each column of the Primer Designer output.
#added desriptions for each column of the Primer Designer output.
 +
[[File:Washington_OldPrimerDesignerdefault.png|left|550px|thumb|Old Default  Primer Designer Output]]

Revision as of 23:46, 21 September 2011


Primer Design Tool with LMU-Munich

We worked with LMU-Munich 2011 iGEM team this summer on the testing and development of their PrimerDesign tool. To learn more about it check out their website.

Software Testing

We helped LMU-Munich test their primer design software by sending our primer data and comparing it with the output of their automated designer. To do this, we compared the sequences of the primers used to amplify out parts of the LuxBrick with the primers that their software designed and concluded that their software works as expected. We also gave feedback on other possible features and spotted a few bugs to fix. Unfortunately, we did not have enough time to order the primers that the software designed to test it ourselves. Overall, we found the tool easy to use and potentially very useful for future primer design.

An example of the output from the tool based off of input from our luxC biobrick, multiple primers with various melting temperatures are given

Implemented Bug Fixes & Features

  1. Added cyanobacteria to available genomes
  2. Switch coding sequences in the primer designer to allow for the user to incude a stop codon in a coding sequence. Before, software insisted that coding sequences not include the stop codon
  3. Made primer designer default to only check for biobrick restriction enzymes. Before, Primer Designer defaulted to checking for all restriction sites, making the user scroll to the bottom of the page for results
  4. added support for FASTA files with headers
  5. added desriptions for each column of the Primer Designer output.
Old Default Primer Designer Output