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	<title>Comments on: Navigenics: The Experience</title>
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	<link>http://chilmarkresearch.com/2009/03/16/navigenics-the-experience/</link>
	<description>Providing perspective on key IT trends in the healthcare sector</description>
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		<title>By: Personal DNA Sequencing Price Dropped by 50%! &#124; angiEmedia</title>
		<link>http://chilmarkresearch.com/2009/03/16/navigenics-the-experience/#comment-3066</link>
		<dc:creator><![CDATA[Personal DNA Sequencing Price Dropped by 50%! &#124; angiEmedia]]></dc:creator>
		<pubDate>Thu, 18 Jun 2009 09:00:06 +0000</pubDate>
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		<description><![CDATA[[...] Navigenics: The Experience [...]]]></description>
		<content:encoded><![CDATA[<p>[...] Navigenics: The Experience [...]</p>
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		<title>By: Gerry Higgins, Ph.D.</title>
		<link>http://chilmarkresearch.com/2009/03/16/navigenics-the-experience/#comment-2642</link>
		<dc:creator><![CDATA[Gerry Higgins, Ph.D.]]></dc:creator>
		<pubDate>Sat, 18 Apr 2009 15:11:16 +0000</pubDate>
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		<description><![CDATA[It is not conclusive, as you suggest, that all genes that convey susceptibility to a given disease have been identified. In fact, the domain is very much in its infancy. However, you can increase the power of the existing genomic information by combining those data with your other personal  health data, as was suggested by Barbara Prainsack and Jenny Reardon in their commentary in Nature (see http://www.nature.com/nature/journal/v456/n7218/full/456034a.html).

Thus, I believe it was irresponsible for the &#039;pioneers&#039; consisting of the first 10 members of the Personal Genome Project to post their genomic data along with their own personal health information (see http://www.personalgenomes.org/pgp10.html).

It not only sets a bad precendent, but it could also harm their offspring when new disease genes are identified, placing not only themselves but also their offspring at risk of not obtaining medical insurance and other coverage (look at the actions of the Medical Information Bureau (MIB), that has been collecting personal health information for years. The MIB is an organization established by the insurance industry (as they describe it, “similar to a credit-reporting agency”) that collects data on individuals
from various healthcare insurance claims. The MIB then distributes this information, correct or not, to the health and life insurance companies as requested).]]></description>
		<content:encoded><![CDATA[<p>It is not conclusive, as you suggest, that all genes that convey susceptibility to a given disease have been identified. In fact, the domain is very much in its infancy. However, you can increase the power of the existing genomic information by combining those data with your other personal  health data, as was suggested by Barbara Prainsack and Jenny Reardon in their commentary in Nature (see <a href="http://www.nature.com/nature/journal/v456/n7218/full/456034a.html" rel="nofollow">http://www.nature.com/nature/journal/v456/n7218/full/456034a.html</a>).</p>
<p>Thus, I believe it was irresponsible for the &#8216;pioneers&#8217; consisting of the first 10 members of the Personal Genome Project to post their genomic data along with their own personal health information (see <a href="http://www.personalgenomes.org/pgp10.html" rel="nofollow">http://www.personalgenomes.org/pgp10.html</a>).</p>
<p>It not only sets a bad precendent, but it could also harm their offspring when new disease genes are identified, placing not only themselves but also their offspring at risk of not obtaining medical insurance and other coverage (look at the actions of the Medical Information Bureau (MIB), that has been collecting personal health information for years. The MIB is an organization established by the insurance industry (as they describe it, “similar to a credit-reporting agency”) that collects data on individuals<br />
from various healthcare insurance claims. The MIB then distributes this information, correct or not, to the health and life insurance companies as requested).</p>
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		<title>By: Bertalan Meskó</title>
		<link>http://chilmarkresearch.com/2009/03/16/navigenics-the-experience/#comment-2411</link>
		<dc:creator><![CDATA[Bertalan Meskó]]></dc:creator>
		<pubDate>Mon, 16 Mar 2009 18:39:53 +0000</pubDate>
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		<description><![CDATA[John, 

Excellent review and very valid points. I&#039;ll link to you post in my Twitter community and will include it in the next Gene Genie blog carnival edition, if you don&#039;t mind.

Thank you for the mention!

Berci]]></description>
		<content:encoded><![CDATA[<p>John, </p>
<p>Excellent review and very valid points. I&#8217;ll link to you post in my Twitter community and will include it in the next Gene Genie blog carnival edition, if you don&#8217;t mind.</p>
<p>Thank you for the mention!</p>
<p>Berci</p>
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		<title>By: Sean Nolan</title>
		<link>http://chilmarkresearch.com/2009/03/16/navigenics-the-experience/#comment-2410</link>
		<dc:creator><![CDATA[Sean Nolan]]></dc:creator>
		<pubDate>Mon, 16 Mar 2009 17:00:43 +0000</pubDate>
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		<description><![CDATA[Hey John ... just a quick follow-up. the Navi folks are still finishing their HealthVault upload --- but it will be done within the next few weeks. 
---S]]></description>
		<content:encoded><![CDATA[<p>Hey John &#8230; just a quick follow-up. the Navi folks are still finishing their HealthVault upload &#8212; but it will be done within the next few weeks.<br />
&#8212;S</p>
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