DNA Quote of the Day - Martin Varsavsky and 23andMe
by Dr. Hsien-Hsien Lei
Posted May 24, 2007 in DNA Quotes and Excerpts
23andMe investor Martin Varsavsky made the following comment in a VentureBeat post about Google’s investment in the personal genome company:
…Having said this it is not really Google here. It is [co-founders] Anne [Wojcicki] and Linda [Avey] running the show and hopefully succeeding at creating a global search engine for human genes that will help us know more about how we are related to each other and how we can fight disease and live longer and better lives.
A global search engine for human genes? Did anyone else get goosebumps after reading that? Or is it just me?
Tags: 23andme, genetics, genes, genome, genomics, dna, diseases, illness, health, medicine, google

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Search giant Google had previous plans to develop a DNA databse if they are not scrapped they still might be more to come
Google’s collaboration with genomic research institute J. Craig Venter, to create a searchable online database of all the genes on the planet,
Google founders Sergey Brin and Larry Page and genome sequencer J. Craig Venter had started collaborating in the area of genetics research in early 2005
http://news.zdnet.co.uk/itmanagement/0,1000000308,39260264,00.htm
If there is any possiblity that it would become a reality I would welcome the move, what with life science and biology becoming one most expensive research fields any attempts to make it cheap and turn out commerical viable solutions faster should be welcomed
As far as concerns of fraud or illicit use of the information available to everyone I guess we have to trust googles good reputations for the beginnign atleast
Thanks for the comment, Albin Paul! I wasn’t sure if I was getting goosebumps from excitement or fear.
FYI for anyone who’s interested, I wrote about allegations against Google and genetic privacy last year over at my old blog, Genetics and Health.
Does Google have a “good reputation?” Not so sure about that one… Yes, a little goosebumpy for me too, Hsien.
You don’t have anything to worry about, Christina, as long as you’re friends with me. I’ve got your back when it comes to all this DNA stuff.
Frankly, I am not clear on exactly what 23andme is going to do. Will people “donate” their DNA samples? How will this data be kept private and confidential? Exactly how will this data be used? Will people who provide their DNA samples be informed of possible future severe health problems based on their DNA analysis? (And how do they know the quality of the analysis?) Will they receive adequate genetic counseling? By whom? Do they really want to KNOW the results if, say, it’s a death sentence such as the case of Huntington’s disease? And I haven’t even touched on the business issues - what is 23andme’s business model, for example. I look forward to learning much more about 23andme!
All good questions, Bruce. Wish I had some answers for ya! Stay tuned.
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