Fork me on GitHub

Playing personal genomics catchup

One week into the year and we have already seen a flurry of personal genomics activity and news.

lifecodeThe first piece of info that caught my eye was that GATC Biotech, a next-gen sequencing service provider and genomics company, had annouced LifeCode, which they call the EU’s first personal genomics company. The company says that they will focus on placing an individual’s genomic data in a “medical context”. I presume that they plan to use next-gen sequencing for their efforts, but the pricing and methodology is not known at this time. The service will launch in April

knomeKnome, which has said it will sequence the entire genome (as opposed to genotyping) for $350K announced a deal with Beijing Genomics Institute for sequencing services

The NEJM’s report on personal genomics, resulted in a flurry of discussion. Notable follow up includes blog posts by Blaine Bettinger and Steve Murphy. I maintain my position that the cat is out of the bag, and there are enough people with money and the interest to use the available services (not all will survive, but some will). Our goal should focus on education, and making sure that people are aware of the risks, not only patients, but also physicians who are having to deal with patients that not only search web resources like WebMD (often second guessing their physicians), but might also come armed with a report listing some potential disease-causing SNPs.

On that note, Paul Kedrosky points to a press release from a public interest group which has this memorable line

basing decisions solely on online hysteria and fear could lead to a public health crisis or even death.

It is true that there is so much information available on the web today that it is difficult to distill it down. It is also true that a little knowledge can be more dangerous than none at all. However, if we are to move towards an aware, educated population, our emphasis should be on the aforementioned education, and a change in approach, where we work with our medical providers to understand what the online information might mean. Physicians shouldn’t feel threatened, and patients should realize that they are not the experts. This “problem” is only going to get worse before things reach a point of equilibrium.

Technorati Tags: , , ,

This entry was posted in Healthcare, Your personal health. Bookmark the permalink. Post a comment or leave a trackback: Trackback URL.

4 Comments

  1. Posted January 12, 2008 at 19:33 | Permalink

    Deepak,
    I totally agree. This will get MUCH worse, before it reaches equilibrium.
    -Steve
    http://www.helixhealth.org

  2. Posted January 12, 2008 at 21:33 | Permalink

    Deepak,
    I totally agree. This will get MUCH worse, before it reaches equilibrium.
    -Steve
    http://www.helixhealth.org

  3. Posted January 13, 2008 at 16:28 | Permalink

    The timing of your blog is interesting. Just last Wednesday the Winter Bioinformatics kick-off event at UMich focused on these topics. In particular, comprehending what personal genomics really means. Clearly it is something accessible to the public. Time will make it moreso.

    I didn’t see a link to the Wired article about 23andMe’s service. I bet you’ve already read it.

    http://www.wired.com/medtech/genetics/magazine/15-12/ff_genomics

    We used this article to prime discussion at the kick-off event. I couldn’t help but notice relatively polarized arguments overall. Two clear trends were present. Everyone seemed to agree that personal genomics is upon us. Everyone also seemed to agree that little to no legal or ethical guidelines exist.

    I’m curious to see what becomes of these new services. ‘Personal proteomics’ and related fields are surely right around the corner….the total body scan folks in the mall will have to make some space.

  4. Posted January 13, 2008 at 18:28 | Permalink

    The timing of your blog is interesting. Just last Wednesday the Winter Bioinformatics kick-off event at UMich focused on these topics. In particular, comprehending what personal genomics really means. Clearly it is something accessible to the public. Time will make it moreso.

    I didn't see a link to the Wired article about 23andMe's service. I bet you've already read it.

    http://www.wired.com/medtech/genetics/magazine/...

    We used this article to prime discussion at the kick-off event. I couldn't help but notice relatively polarized arguments overall. Two clear trends were present. Everyone seemed to agree that personal genomics is upon us. Everyone also seemed to agree that little to no legal or ethical guidelines exist.

    I'm curious to see what becomes of these new services. 'Personal proteomics' and related fields are surely right around the corner….the total body scan folks in the mall will have to make some space.

Post a Comment

Your email is never published nor shared. Required fields are marked *

*
*

You may use these HTML tags and attributes: <a href="" title=""> <abbr title=""> <acronym title=""> <b> <blockquote cite=""> <cite> <code> <del datetime=""> <em> <i> <q cite=""> <strike> <strong>

blog comments powered by Disqus
  • Archives

  • Disclaimer

    All opinions on this blog are my own and do not reflect those of my employers, past or present