Team:VT-ENSIMAG/User primer

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This tool will be useful also for biologist working on the VBI lab, as they had to do it manually before, and it was pretty slow and subject to human errors.
This tool will be useful also for biologist working on the VBI lab, as they had to do it manually before, and it was pretty slow and subject to human errors.
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Example: here is a detailled example of an extraction of PCR primers.
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[[Image:PCR2.jpg|590px|center]]
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Revision as of 10:23, 28 September 2010


VT-ENSIMAG over VT campus long.png

Helping an iGEM team




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Home

Our team

Sequence screening

The software: GenoTHREAT

Tests and Results

Screening of the iGEM registry

PCR fusion primer

Lab notebook

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In addition of screening the entire iGEM registry, we have developed a tool to help a biology iGEM team. This team is the Virginia United team. A part of this team was indeed working at Virginia Bioinformatics Institute, so we had the opportunity to meet each other. It consisted in finding the DNA sequence of the primer, given three input sequences: the two sequences that will undergo the PCR, and the complete resulting sequence.

The software will find 4 primers: the forward primer overlapping with the first input, the reverse user primer that overlaps with the first sequence and the gap sequence added on the PCR, the forward user sequence, overlapping with the second sequence and the gap sequence, and endly the reverse primer, which overlaps with the second sequence. If some suffix, prefix or terminator are added on the full sequence, they will be added in the forward and reverse primers. To detect the length of the overlapping part of the primers, we search for the correct length that will have the desired melting temperature. This melting temperature is calculated with the equation:

deltaH
Tm = ----------------------------------------- - 273.15 + 16.6log[Na+]
-10.8 + deltaS + Rln([oligo]/4)

with R = 1.987 cal/(mol K) Gas constant, [oligo] = 5E-07 M, [Na+] = 0.05 M. The find the position of the cutting enzyme (where the nucleotide U was placed), we search for an A in the gap sequence, and a matching T 8~13bp further. The A will be replaced by the U in the reverse user primer, and the T will be replace by the U in the forward user primer.

This tool will be useful also for biologist working on the VBI lab, as they had to do it manually before, and it was pretty slow and subject to human errors.


Example: here is a detailled example of an extraction of PCR primers.

PCR2.jpg


An executable with explanantions to use it (on windows or on linux) are available here:_________. This software can be used with the interface shown previously, or with command line only (to automatisized it easily). The input can be the 3 sequences or a file containing these 3 sequences. The source code of this software is also available ____________.

ALIEN DNA.png
VT-ENSIMAG logo.png
ALIEN DNA.png