Ask yourselves.... how much progress could be made in Vitiligo research if scientist shared the DNA samples that they have taken from Vitiligo Patients?
Take it one-step further...How many people with Vitiligo would gladly pay a nominal fee to ship their DNA to a testing facility?
I want to start a free DNA library to support Vitiligo research, can it be done? What challenges do we face?
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My goals would be to:
1) Consolidate the existing DNA samples of Vitiligo patients that have already participated in a study.
2) Set up a DNA submission and testing process (see link) - Honestly I don't know one person with Vitiligo that wouldn't submit a saliva sample to help find a cure.
3) Then someway, there needs to be universal access to the data, so researchers can isolate the problem.
4) My last goal would be to set up an incentive, a jackpot fund, for the person/institution that finds a cure (this part would probably break non-profit guidance laws).
The challenge isn't so much setting up the DNA testing part, it's getting people to work together and share research.
Vitiligo is in limbo land when it comes to research and analysis. If pharmaceutical companies don't make a lot of money
treatingmaintaining the disease, there will not be a lot of research grants. And since its not life threatening, it drops even further down the totem pole of attention (in our medical world). My boss would call it the "zone of indifference".1.) Probably need a 501c3 (non-profit) entity.
2.) You'll need to help explain to people how their DNA data will be used and protected. Privacy is a big factor for most (HIPPA?).
3.) Find out how (logistically) people can send/ship their data. How much will it cost? How much time does it take? What types of facilities do people need to go to?
4.) With the data, what should we be looking for? DNA data is huge, we need some smart-ass people who know what they are looking for.
There was an article recently (if i remember correctly) about scientists comparing the DNA from people with vitiligo and the general population about melanoma. (http://news.suite101.com/article.cfm/gene-variant-in-vitiligo-prote...) ... they might already have a large set of data already.
Again, this is just my first thoughts. I might be totally wrong. :)