23andMe makes personalized genetics more affordable

http://www.23andme.com/

by russ • 18 years ago

15 15 18 years ago

23andme.com

mechanical_fish• 18 years ago

Still a little expensive, but downright fascinating. Someone has put a heck of a lot of time into this.

It looks like they give you your own raw genomics data! Fun fun fun!

vaksel• 18 years ago

so I guess this means the injunction was lifted?

russ4• 18 years ago

We are officially licensed in California, NY is still pending.

brfox2• 18 years ago

Let me know when you've got a 454 or Solexa, then I'll sign up... :)

chaostheory• 18 years ago

Great news =)

Good but here are things that will help me bite:

- $299-199

- a better database for people with Asian heritage. I could be wrong but I think no company in the West has this yet - well a company in Greenland is working on a partnership with a Hong Kong company

- something like HIPAA or some privacy clause. I don't want my insurance companies to know I'm genetically prone to X

- I'm not keen on someone trying to patent my genes either (don't know if you guys will or not though)

russ4• 18 years ago

To address some of the things you mentioned:

- as we add more people to our database (including Asians), we can make new discoveries relevant to particular genetic groups

- GINA prohibits employers/insurers from discriminating against you based on your genetic info

- we will not patent genes. we want to empower people by giving them the ability to access and interact with their genetic information

natch• 18 years ago

>GINA prohibits employers/insurers from discriminating against you based on your genetic info

Laws change. And the value of words like "discriminating" also changes with various interpretations.

There are right and wrong ways to protect the privacy of customers. Relying on laws is one of the wrong ways.

pius• 18 years ago

GINA prohibits employers/insurers from discriminating against you based on your genetic info

That's an incredibly weak response. Someone asks you about the privacy you provide and you say it's illegal for other people to misuse the information. That's like me asking a company what they're going to do with and how they're going to protect my social security number and the company rep pausing and saying "Um, yeah . . . don't worry, identity fraud is illegal." Not the most confidence inspiring thing I've ever heard.

I spent several years in the privacy sector and take it from me that protecting this kind of information is hard enough when the organization actually has a commitment to meeting industry standard privacy best practices and laws, let alone at a company that apparently ignores them. (Please correct me if your company actually does comply with HIPAA or any other federal privacy laws -- I'm just going by you responding to a question about your privacy compliance by rattling off a reference to some newly-passed law that is non-binding on your company.)

Relying on GINA here is completely irresponsible. If you're serious about handling sensitive health information, you ought to comply with HIPAA and have that compliance routinely audited. Period.

Otherwise no one should trust your company or, in my opinion, take it seriously at all.

gleb• 18 years ago

I hate to be negative about a startup that way, but it's important to realize that "direct-to-consumer genomics" is a scam. I went to a presentation by a founder of one the competitors (there are 3-4 high-flying competitors in the business), and I had the highest expectations. But then throughout the presentation I couldn't quite figure out what the company actually does. So I asked. And the answer is marketing and litigation.

* these companies don't do any research

* they don't even own sequencing equipment

* all they do is send a sample of your spit to the lab, and send you a pretty writeup

* consider why is there no "direct-to-consumer blood tests" even though that information is far more actionable

I wouldn't even have a problem with this if it was a proper scam, like XanGo MLM, a nice nutritional supplement scheme, make-money-fast setup, etc. With these you know upfront what you are getting into. But these guys look so clean, and go out of their way to skate the narrow line next to the true medical advice. Needless to say the legal budgets must be non-trivial.

I ran this by my cousin who is in nursing school. And she goes "Oh yuh, they are teaching us how to talk to people about all the nonsense results people [in increasing numbers] will get through these outfits."

Some more reading: http://microarray.wordpress.com/2008/06/24/deadline-today-fo...

russ4• 18 years ago

Not sure all personalized genetics companies are created equal. You seem to be pretty misinformed about what we do.

* We indeed do conduct our own research and are currently collaborating with some prominent research institutions (Parkinson's institute).

* Why do we have to own sequencing equipment to be useful and/or legit? Does Google own the webpages they index?

* We give you much more than a "pretty writeup". This includes crowd-sourced research initiatives, ancestry and health communities, and many interactive ways of analyzing your own data. A ton more things coming in the future.

huhtenberg• 18 years ago

Just to clarify, is this you - https://www.23andme.com/about/advisors ? Thanks.

sungam• 18 years ago

The problem with SNP-based association is that, for the vast majority of disease-associated SNPs, the relative risk is only increased on the order of a few percent at most. When it comes to predicting the risk of an individual (as opposed to a population) developing a particular disease this is virtually meaningless. No doubt the current technology will appeal to some out of curiosity. However I do think that the vast quantities of sequence that will be generated by next generation platforms over the next few years will lead to the ability to usefully predict disease susceptibility of an individual basis.

23andMe makes personalized genetics more affordable

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