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2.5 KiB
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38 lines
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2.5 KiB
HTML
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<title>
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Comments on: Open Access! Million Veteran Program Genome-Wide PheWAS Results Now Available in dbGaP! </title>
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<link>https://ncbiinsights.ncbi.nlm.nih.gov/2024/07/22/million-veteran-program-dbgap/</link>
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By: John Hasty </title>
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<link>https://ncbiinsights.ncbi.nlm.nih.gov/2024/07/22/million-veteran-program-dbgap/comment-page-1/#comment-128292</link>
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<dc:creator><![CDATA[John Hasty]]></dc:creator>
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<pubDate>Mon, 22 Jul 2024 18:36:27 +0000</pubDate>
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<guid isPermaLink="false">https://ncbiinsights.ncbi.nlm.nih.gov/?p=13612#comment-128292</guid>
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<description><![CDATA[This type of connectivity is definitely a step in the right direction. I have my VA blood testing done every 6 months and I am essentially interested in my thyroid chemistries. My genome sequencing data done at Nebula indicates a predisposition for thyroid problems. It would be interesting if a MVP participant could download their sequencing data from the MVP for personal comparison and evaluation.
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An even bigger step in the right direction would be to connect all participants with a single condition or trait with their related blood work values. Thanks for the great job!]]></description>
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<content:encoded><![CDATA[<p>This type of connectivity is definitely a step in the right direction. I have my VA blood testing done every 6 months and I am essentially interested in my thyroid chemistries. My genome sequencing data done at Nebula indicates a predisposition for thyroid problems. It would be interesting if a MVP participant could download their sequencing data from the MVP for personal comparison and evaluation.</p>
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<p>An even bigger step in the right direction would be to connect all participants with a single condition or trait with their related blood work values. Thanks for the great job!</p>
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