[dluan]

One of the biggest challenges they've had to and continue to try to overcome is an outdated policy system around personal health data, within the U.S., and I'm not sure if Jack Andraka has attempted to mass produce and mass release his pancreatic kit. The statement was about their recent FDA battles, not about 'advancing science'.

The 23andme dataset provides more value than HGP since it's an dataset of active participants. I don't know too much about the specifics or privacy mechanics, so I can't comment on how, but this article is an example (http://www.mercurynews.com/science/ci_27487046/23andme-quest...). The way researchers are using the dataset is very different because they are able to do followups. That's a very significant difference, it's why they have pharma companies lining up to get access to the dataset.

Last I heard, they were closer to 1M than 850k, unfortunately can't find any live stats. Maybe someone else can chime in?

I don't have any affiliation, and I'm surprised that you'd assume so. I recognize that there's an overeagerness from both startup people and academics to crap on biotech startups, rightly or wrongly. I haven't quite figured out why spectators are motivated to do so.

[jghn]

One big negative is that they're only running a snp pnel for most cases and just now starting to toe the water of exomes