Virginia Tech/Updates
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- | + | <a href="https://2007.igem.org/Virginia_Tech"><h3>Home</h3></a> | |
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+ | <a href="https://2007.igem.org/Virginia_Tech/Project"><h3>TheProject</h3></a> | ||
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+ | <a href="https://2007.igem.org/Virginia_Tech/Team"><h3>OurTeam</h3></a> | ||
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+ | <a href="https://2007.igem.org/Virginia_Tech/Updates"><h3>Progress</h3></a> | ||
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+ | <a href="https://2007.igem.org/Virginia_Tech/JC"><h3>JournalClub</h3></a> | ||
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+ | <a href="https://2007.igem.org/Virginia_Tech/Links"><h3>Links</h3></a> | ||
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- | < | + | <h3>On this page we will periodically publish updates on our progress.</h3> |
- | </ | + | We maintain an internal wiki on a daily basis. Here we will post highlights from that wiki as well as important milestones as we reach them. Click one of the section headings below to read about our recent progress. |
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- | + | [[Virginia_Tech/Updates/Modeling|Modeling]] | |
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- | + | The model and computer simulations of the infection. | |
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- | + | • Skip to [[Virginia_Tech/Updates/Modeling/Infection_Model|One Population Infection Model]] | |
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+ | • Skip to [[Virginia_Tech/Updates/Modeling/PopInter_Model|Population Interaction Model]] | ||
+ | [[Virginia_Tech/Updates/Phage|Phage Culture]] | ||
+ | Growing and manipulating phage lysates, observing their interaction with cells. | ||
+ | [[Virginia_Tech/Updates/Plasmid|Reporter Plasmid]] | ||
+ | Engineering the plasmid and transforming it into E. coli. | ||
+ | • Skip to [[Virginia_Tech/Updates/Plasmid/Design|Design of the Reporter Plasmid]] | ||
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Revision as of 00:13, 17 October 2007
On this page we will periodically publish updates on our progress.We maintain an internal wiki on a daily basis. Here we will post highlights from that wiki as well as important milestones as we reach them. Click one of the section headings below to read about our recent progress.
The model and computer simulations of the infection. • Skip to One Population Infection Model • Skip to Population Interaction Model Growing and manipulating phage lysates, observing their interaction with cells. Engineering the plasmid and transforming it into E. coli. • Skip to Design of the Reporter Plasmid
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