Team:PoznanBioInf

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<h1 >WELCOME TO iGEM 2014! </h1>
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<h2>MUFASA: Multiple fragments assembler for scarless cloning of big genetic constructs.</h2>
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<p>Your team has been approved and you are ready to start the iGEM season!
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<br>On this page you can document your project, introduce your team members, document your progress <br> and share your iGEM experience with the rest of the world! </p>
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Overlap-based cloning techniques like Gibson Assembly and Circular Polimerase Extension Cloning (CPEC) have been recently becoming more and more popular. While available software allows rapid overlap design for constructs of conventional size, details of its functioning are not always fully transparent. MUFASA aims not only at facilitating the scarless cloning from the oligonucleotide design to putting the tubes into the thermocycler, but also at designing the fragments themselves in parallel with the overlaps for synthesis of big constructs de novo. Use of multiple overlaps pose a risk of non-specific hybridization and overlap “shadowing”. Such “shadowy places” may be eliminated by thermodynamic sequence optimization of both CPEC primers and fragments of the desired construct.
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<p style="color:#E7E7E7"> <a href="https://2014.igem.org/wiki/index.php?title=Team:PoznanBioInf&action=edit"style="color:#FFFFFF"> Click here  to edit this page!</a> </p>
<p style="color:#E7E7E7"> <a href="https://2014.igem.org/wiki/index.php?title=Team:PoznanBioInf&action=edit"style="color:#FFFFFF"> Click here  to edit this page!</a> </p>

Revision as of 20:27, 5 September 2014


MUFASA: Multiple fragments assembler for scarless cloning of big genetic constructs.

Overlap-based cloning techniques like Gibson Assembly and Circular Polimerase Extension Cloning (CPEC) have been recently becoming more and more popular. While available software allows rapid overlap design for constructs of conventional size, details of its functioning are not always fully transparent. MUFASA aims not only at facilitating the scarless cloning from the oligonucleotide design to putting the tubes into the thermocycler, but also at designing the fragments themselves in parallel with the overlaps for synthesis of big constructs de novo. Use of multiple overlaps pose a risk of non-specific hybridization and overlap “shadowing”. Such “shadowy places” may be eliminated by thermodynamic sequence optimization of both CPEC primers and fragments of the desired construct.


Click here to edit this page!

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