Math Questions
From 2006.igem.org
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* What is the distribution of the number of flips required, if each flip is random?<br> | * What is the distribution of the number of flips required, if each flip is random?<br> | ||
* What designs might allow us to track flips made?<br> | * What designs might allow us to track flips made?<br> | ||
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* Can we create "dummy" pieces of DNA to measure rate and frequency of flipping? | * Can we create "dummy" pieces of DNA to measure rate and frequency of flipping? | ||
* Can we create a series of target sites (e.g. LLLLL --------- RRRRRR) such that any one of several flip sites can be chosen and if hixC is dead end, we could continue flipping? | * Can we create a series of target sites (e.g. LLLLL --------- RRRRRR) such that any one of several flip sites can be chosen and if hixC is dead end, we could continue flipping? | ||
| + | * Can we incorporate probabilities for flipping regions into our model? | ||
Revision as of 14:17, 13 June 2006
- What is the distribution of the number of flips required, if each flip is random?
- What designs might allow us to track flips made?
- Can we model the distance of RE from pancake vs. time or number of flips
- Can we model the kinetics of n flips?
- Is it possible to simulate the impact of one-time flipping lox/hix sites?
- Help us design the fewest number of constructs that will allow us to scale up the number of flips in our constructs (1, 2, 3, 4...n)
- How can we count the number of Flips? (even vs. odd only?)
- Can we use antibiotic resistence percentage (100% vs. 50% to determine number of flips for a single pancake?
- Can we create "dummy" pieces of DNA to measure rate and frequency of flipping?
- Can we create a series of target sites (e.g. LLLLL --------- RRRRRR) such that any one of several flip sites can be chosen and if hixC is dead end, we could continue flipping?
- Can we incorporate probabilities for flipping regions into our model?
