Team:Shenzhen BGIC 0101/Home

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Revision as of 19:30, 26 September 2013 by Czh (Talk | contribs)

igem
  • 1All members of our team.
  • 2Nucleotide modification allow users to modify sequence as their wishes by utilizing codon synonomousness.
  • 3We can help you creat a new chromosome.
  • 4Genove can help you design a new pathway.
  • 5test
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Genovo

Genovo is a Computer-Aided Design(CAD) tool to create genome denovo. The current version is 1.2. It consists of 10 plugins belonging to 3 design modules.
The first module, NeoChr, would assist users to grab related genes in different pathways manually, to rewire genes’ relationship logically, and to replace genes with ortholog that score higher. Then it would allow users to define gene order and orientation in DRAP&DROP way, and add chromosome features to build a brand new genome automatically.
The second one , NucleoMod, would optimize the CDS regions and reduce their synthesis difficulty. And it helps design the CRIPSR site so that we can silence the wild type genes, and in the meanwhile, differentiate the wild type and synthesis type when assemling. This module also can erase or create enzyme site locally.
The third one, SegmMan will cut chromosome into pieces with different sizes with Gibson, Goldengate, Homologous adaptors to them so that they are able to be assembled into whole experimentally.
SegmMan, in another level, provide a complementary OLSDesign will guide users to get the chrosome fragments by chip and how to assembly them together.

  • SegmMan

    SegmMan

    SegmMan will cut chromosome into pieces with different sizes with Gibson, Goldengate, Homologous adaptors to them so that they are able to be assembled into whole experimentally. SegmMan, in another level, provide a complementary OLSDesign will guide users to get the chrosome fragments by chip and how to assembly them together.

    more →
  • NucleoMod

    Nucleotide Modification

    NucleoMod, would optimize the CDS regions and reduce their synthesis difficulty. And it helps design the CRIPSR site so that we can silence the wild type genes, and in the meanwhile, differentiate the wild type and synthesis type when assemling. This module also can erase or create enzyme site locally.

    more →
  • NeoChr

    NeoChr

    NeoChr, would assist users to grab related genes in different pathways manually, to rewire genes’ relationship logically$1, and to replace genes with ortholog that score higher$2. Then it would allow users to define gene order and orientation in DRAP&DROP way, and add chromosome features to build a brand new genome automatically

    more →