23andMe, the personal genetics company has begun a new program funded in part by Google co-founder Sergey Brin. They are now looking for at least 10,000 PD patients to provide genetic samples and answer questionnaires about their own health experiences.
23andMe takes DNA samples from individuals (people spit in a cup) and then help them read and understand the results. The information provided includes data about ancestry, inherited traits and disease risk. Because their service is web based, they can get both specific information about a person's background (phenotype) through questionnaires as well as their genetic profile (genotype) via the DNA samples. This makes them a perfect central repository for genome-wide association studies (GWAS).
By centralizing the recruitment of individuals, the lab work and the collection of phenotypic data, we believe we’ll be able to move beyond traditional hurdles and take GWAS to a whole new level that we’re calling Research 2.0. We think the study of human disease and drug response deserves the application of 21st century technology, including the use of social networking tools proving so effective in web-based sharing of information à la Facebook and YouTube.
They are working with the Michael J. Fox Foundation and the Parkinson's Institute. As a person with Parkinson's (PWP), I am happy about the study and hope it yields some interesting results. I have requested a discount code via this link at the Michael J. Fox Foundation and encourage any PWP to do the same. The cost will be $25 vs. the standard $399 rate, and you will get all of the standard ancestry, inherited traits and disease risk information as well as the ability to participate in a Parkinson's specific community on their website.