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| <p> | | <p> |
- | Neochr module uses public data from <a href="www.yeastgenome.org">Saccharomyces Genome Database</a>, <a href="www.genome.jp/kegg">Kyoto Encyclopedia of Genes and Genomes</a> , <a href="www.genome.wisc.edu">E.coli genome project</a>,<a href="www.mgc.ac.cn/VFs/main.htm"> Virulence Factors of Pathogenic Bacteria </a>.<br/>Neochr module 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*. Firstly, it would allow users to define gene order and orientation in DRAG&DROP way. Secondly, decoupled these genes if have overlap and make all genes are non-redundancy. Finally, add chromosome features to build a new chromosome and show in the JBrowse. Moreover, users can drag a window in the JBrowse and delete any gene in the window. <br/> | + | Neochr module uses public data from <a href="www.yeastgenome.org">Saccharomyces Genome Database</a>, <a href="www.genome.jp/kegg">Kyoto Encyclopedia of Genes and Genomes</a> , <a href="www.genome.wisc.edu">E.coli genome project</a>,<a href="www.mgc.ac.cn/VFs/main.htm"> Virulence Factors of Pathogenic Bacteria </a>.<br/> |
- | After constructing a new chromosome, the next step is NucleoMod module which is to modify CDS based on synonymous mutation.
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- | </p>
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| <img src="https://static.igem.org/mediawiki/2013/1/11/Mm3.jpg" /> | | <img src="https://static.igem.org/mediawiki/2013/1/11/Mm3.jpg" /> |
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| <img src="https://static.igem.org/mediawiki/2013/5/5d/M4.jpg" /> | | <img src="https://static.igem.org/mediawiki/2013/5/5d/M4.jpg" /> |
| <img src="https://static.igem.org/mediawiki/2013/2/2f/Mm1.jpg" /> | | <img src="https://static.igem.org/mediawiki/2013/2/2f/Mm1.jpg" /> |
- | <img src="https://static.igem.org/mediawiki/2013/b/bf/Mm2.jpg" /><br/><br/> | + | <img src="https://static.igem.org/mediawiki/2013/b/bf/Mm2.jpg" /><br/> |
| + | The Neochr module contains three plugins: Decouple, Add and delete.<br/> |
| + | <img src="https://static.igem.org/mediawiki/2013/9/91/Decpuple.png" /><br/> |
| + | <img src="https://static.igem.org/mediawiki/2013/a/a7/Add.png" /><br/> |
| + | <img src="https://static.igem.org/mediawiki/2013/8/8c/Delete.png" /><br/> |
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| + | </p> |
| + | <br/> |
| <h2>NucleoMod</h2> | | <h2>NucleoMod</h2> |
- | <p>NucleoMod is a module to modity CDS sequence of genes which generated by Neochr module. This module contains 5 plugins: CRISPR design, erase enzyme site, create enzyme site, codon optimization, repeat smash. All of these plugin is allow user to change or optimize the gene. After NucleoMod operation, the next step is SegmMan to design synthestic method according to the length of chromosome.</p><br/><br/> | + | <p>When we extract gene from wild type genome to create a new chromosome, We need to silence the original wild type gene. The NucleoMod module can design CRISPR site to reach this goal. And the module can optimize the codon to increase expression level of genes. |
| + | <img src="https://static.igem.org/mediawiki/2013/8/82/Crispr-01.png" /><br/> |
| + | <img src="https://static.igem.org/mediawiki/2013/0/09/Create_enzyme_site-01.png" /><br/> |
| + | <img src="https://static.igem.org/mediawiki/2013/2/2f/Erase_enzyme_site-01.png" /><br/> |
| + | <img src="https://2013.igem.org/File:Codon_optization-01.png" /><br/> |
| + | <img src="https://static.igem.org/mediawiki/2013/4/42/Repeat_smash-01.png" /><br/> |
| + | </p><br/><br/> |
| <h2>SegmMan</h2> | | <h2>SegmMan</h2> |
- | <p></p><br/> | + | <p>The synthesizer or synthesis chip can up to 3kb DNA sequence with high accuracy, but chromosome is not that short.<br/> |
| + | SegmMan can settle this problem, it splits chromosome into 30k fragments, after parsing its exited enzyme sites, continues segmentation into 10k and 2k fragments. In 10k and 2k level, its will add vector homologous region and design enzyme sites.<br/> |
| + | <img src="https://static.igem.org/mediawiki/2013/e/ec/Segmentation_principle_general.jpg" /><br/> |
| + | </p><br/> |
| <h2>Others</h2> | | <h2>Others</h2> |
| <p>Presentation from KGML<br/> | | <p>Presentation from KGML<br/> |