Difference between revisions of "Part:BBa K4347005:Design"

(→‎Conserved Motif Analysis)
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The BL primer was designed using [whichever software works].  
 
The BL primer was designed using [whichever software works].  
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===References===
 
===References===
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1. https://journals.plos.org/ploscompbiol/article?id=10.1371/journal.pcbi.1008991
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1. Nystrom, S. L., &amp; McKay, D. J. (2021). Memes: A motif analysis environment in R using tools from the meme suite. PLOS Computational Biology, 17(9). https://doi.org/10.1371/journal.pcbi.1008991

Revision as of 19:46, 22 July 2022

Backward Loop primer (BL)


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]

Conserved Motif Analysis

To detect STEC E.coli strains, campylobacter, shigella and salmonella strains in water, a conserved motif analysis was ran through the MEME SUITE software[1] to compare 16s rRNA regions of these pathogens. Over 400 16s rRNA regions for different strains of STEC E.coli, campylobacter, shigella and salmonella were extracted from the NCBI gene databank and complied into a FASTA file which was ran on MEME SUITE. Extremely high conservation was found between the 16s rRNA regions from these pathogens, thus a universal set of LAMP primers was designed for these pathogens and were vailaded through laboratory experiments.

MEME SUTIE conserved motif analysis. Each colour represents a conserved motif and each line a different pathogen/strain.

BL Design

The BL primer was designed using [whichever software works].


References

1. Nystrom, S. L., & McKay, D. J. (2021). Memes: A motif analysis environment in R using tools from the meme suite. PLOS Computational Biology, 17(9). https://doi.org/10.1371/journal.pcbi.1008991