Difference between revisions of "User:Pakpoom Subsoontorn/Notebook/Genetically Encoded Memory"

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(TO DO List)
(Conceptual questions)
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==Project Description/Abstract==
* Our review paper on [[Media:GeneticEncodeMemory.pdf |genetically encoded memory ]] (in preparation)
*  [[User:Pakpoom Subsoontorn/Notebook/Genetically Encoded Memory/2008/10/10 | Summary note on site-specific recombinase]]
# Application
# Grand Challenges
# Start-up experiments
# Review Articles
==Project List==
* [[User:Pakpoom Subsoontorn/Notebook/Genetically Encoded Memory/2008/10/06| Synthetic Jumping DNA from Integrase/excisionase system]]
*[[User:Pakpoom Subsoontorn/Notebook/Genetically Encoded Memory/2008/10/12 |Implementing N-bit memory with DNA recombination]]
*[[User:Pakpoom Subsoontorn/Notebook/Genetically Encoded Memory/2008/10/15 |Engineering cell-cycle reporter]]
* [[User:Pakpoom Subsoontorn/Notebook/Genetically Encoded Memory/2008/10/14 |Quantitative functional profiles (Database) of site-specific recombinase]]
* [[User:Pakpoom Subsoontorn/Notebook/Genetically Encoded Memory/2008/10/11 |Expanding Integrase/excisionase library]]
==Conceptual questions==
* In the abstract level, how could we live with imperfect efficiency? No matter writing mechanism we choose in the end, the fraction of cells whose genome is actually rewritten will likely to be significantly less than a hundred percent.
* What are the common/ different challenges between writing memory to DNA versus gene therapy/ transgenic?
* Why reaction line DNA integration is irreversible but mostother don't?
==TO DO List==
* [[User:Pakpoom Subsoontorn/Notebook/Genetically Encoded Memory/2008/10/09 |reading]]
* Next meeting: mention storyboard on interesting paper
* Next meeting: mention DNA-pol in vitro selection and in vivo mutagenesis
* read the poster detail from synbio 4.0, esp memory
* Write up the detail structure and mechanism of integrase
* discuss HT-in vivo protein evolution project with Jennifer, James, Quake's pp
* Maybe I should start focusing on specific memory encoding problem..like counting the number of cell cycle.
..many signaling protein rise and fall in each cell cycle, so as the copy number of genome..we might be able
to make use of them.
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Revision as of 19:16, 18 February 2011

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