Difference between revisions of "Csc334 DT lab Ideas"

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* Get familiar with Proce55ing [[CSC334_Lab0| Lab #0]]
 
* Get a DNA sequence [[CSC334_Lab1| Lab #1]]
 
* Get a DNA sequence [[CSC334_Lab1| Lab #1]]
 
* Get a protein sequence [[CSC334_Lab2 | Lab #2]]
 
* Get a protein sequence [[CSC334_Lab2 | Lab #2]]
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* BLAST lab: take a sequence (protein and/or DNA) and find other sequences that are close to it
 
* BLAST lab: take a sequence (protein and/or DNA) and find other sequences that are close to it
 
* given N sequences that overlap, find the best way in which they form a long sequence.  Use processing and a circle approach to represent them
 
* given N sequences that overlap, find the best way in which they form a long sequence.  Use processing and a circle approach to represent them
* display alignment of two sequences
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* display alignment of two sequences [[CSC334_Lab3| Lab #3]]
 
** limit to end to end overlapping
 
** limit to end to end overlapping
 
** from output of blast
 
** from output of blast

Revision as of 09:21, 24 July 2008

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  • Get familiar with Proce55ing Lab #0
  • Get a DNA sequence Lab #1
  • Get a protein sequence Lab #2
  • given a series of nucleotides, find and display the 6 reading frames
  • finding repeats within a sequence
  • BLAST lab: take a sequence (protein and/or DNA) and find other sequences that are close to it
  • given N sequences that overlap, find the best way in which they form a long sequence. Use processing and a circle approach to represent them
  • display alignment of two sequences Lab #3
    • limit to end to end overlapping
    • from output of blast
    • from result of computing local alignment
  • Orfing: (page 146) Finding a sequence longer than some number (proteins are typically 350 residues in length, and at least 100 minimum), between a start (ATG), and a stop (TAA, TAG, TGA) sequence.
  • FoldIt.png


FoldIt! http://fold.it. Read NYT Article If You Have a Problem, Use Innocentive to Ask Everyone for background.











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