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	<title>Portable Genomics&#039; Blog</title>
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	<link>http://portablegenomics.wordpress.com</link>
	<description>Your Genome Different</description>
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		<title>Portable Genomics&#039; Blog</title>
		<link>http://portablegenomics.wordpress.com</link>
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		<title>Mapping copy number variation by population-scale genome sequencing</title>
		<link>http://portablegenomics.wordpress.com/2011/02/07/mapping-copy-number-variation-by-population-scale-genome-sequencing/</link>
		<comments>http://portablegenomics.wordpress.com/2011/02/07/mapping-copy-number-variation-by-population-scale-genome-sequencing/#comments</comments>
		<pubDate>Mon, 07 Feb 2011 11:25:57 +0000</pubDate>
		<dc:creator>Vekris Antoine</dc:creator>
				<category><![CDATA[Antoine&#039;s picks]]></category>

		<guid isPermaLink="false">https://portablegenomics.wordpress.com/?p=303</guid>
		<description><![CDATA[Mapping copy number variation by population-scale genome sequencing Ryan E. Mills et al. Nature 470, 59–65 doi:10.1038/nature09708 Genomic structural variants (SVs) are abundant in humans, differing from other forms of variation in extent, origin and functional impact. Despite progress in SV characterization, the nucleotide resolution architecture of most SVs remains unknown. We constructed a map [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=portablegenomics.wordpress.com&amp;blog=9871701&amp;post=303&amp;subd=portablegenomics&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
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		<slash:comments>0</slash:comments>
	
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			<media:title type="html">antoinevekris</media:title>
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		<item>
		<title>Imputation of sequence variants for identification of genetic risks for Parkinson&#8217;s disease. The Lancet, Early Online Publication, 2 February 2011</title>
		<link>http://portablegenomics.wordpress.com/2011/02/03/imputation-of-sequence-variants-for-identification-of-genetic-risks-for-parkinsons-disease-the-lancet-early-online-publication-2-february-2011/</link>
		<comments>http://portablegenomics.wordpress.com/2011/02/03/imputation-of-sequence-variants-for-identification-of-genetic-risks-for-parkinsons-disease-the-lancet-early-online-publication-2-february-2011/#comments</comments>
		<pubDate>Thu, 03 Feb 2011 05:11:36 +0000</pubDate>
		<dc:creator>pmerel</dc:creator>
				<category><![CDATA[Patrick&#039;s picks]]></category>
		<category><![CDATA[genetic]]></category>
		<category><![CDATA[genomic]]></category>
		<category><![CDATA[medicine]]></category>

		<guid isPermaLink="false">https://portablegenomics.wordpress.com/?p=301</guid>
		<description><![CDATA[Imputation of sequence variants for identification of genetic risks for Parkinson&#8217;s disease: a meta-analysis of genome-wide association studies: &#8220;The discovery phase consisted of 5333 case and 12 019 control samples, with genotyped and imputed data at 7.689.524 SNPs. The replication phase consisted of 7053 case and 9007 control samples. We identified 11 loci that surpassed the [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=portablegenomics.wordpress.com&amp;blog=9871701&amp;post=301&amp;subd=portablegenomics&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
		<wfw:commentRss>http://portablegenomics.wordpress.com/2011/02/03/imputation-of-sequence-variants-for-identification-of-genetic-risks-for-parkinsons-disease-the-lancet-early-online-publication-2-february-2011/feed/</wfw:commentRss>
		<slash:comments>0</slash:comments>
	
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			<media:title type="html">pmerel</media:title>
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		<item>
		<title>DNAVISION, Belgium</title>
		<link>http://portablegenomics.wordpress.com/2011/01/18/dnavision-belgium/</link>
		<comments>http://portablegenomics.wordpress.com/2011/01/18/dnavision-belgium/#comments</comments>
		<pubDate>Tue, 18 Jan 2011 06:39:27 +0000</pubDate>
		<dc:creator>Oldcola</dc:creator>
				<category><![CDATA[Antoine&#039;s picks]]></category>

		<guid isPermaLink="false">https://portablegenomics.wordpress.com/?p=285</guid>
		<description><![CDATA[Dans un premier temps, DNAVision s’appuyera sur ces systèmes [systèmes SOLiD™ de Life Technologies] pour proposer le séquençage complet du génome humain [au prix de 7,500 €] pour les acteurs du monde pharmaceutique et de la recherche médicale. Source (pdf)<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=portablegenomics.wordpress.com&amp;blog=9871701&amp;post=285&amp;subd=portablegenomics&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
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		<slash:comments>0</slash:comments>
	
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			<media:title type="html">Oldcola</media:title>
		</media:content>
	</item>
		<item>
		<title>Maternal Plasma DNA Sequencing Reveals the Genome-Wide Genetic and Mutational Profile of the Fetus</title>
		<link>http://portablegenomics.wordpress.com/2011/01/16/maternal-plasma-dna-sequencing-reveals-the-genome-wide-genetic-and-mutational-profile-of-the-fetus/</link>
		<comments>http://portablegenomics.wordpress.com/2011/01/16/maternal-plasma-dna-sequencing-reveals-the-genome-wide-genetic-and-mutational-profile-of-the-fetus/#comments</comments>
		<pubDate>Sun, 16 Jan 2011 15:22:46 +0000</pubDate>
		<dc:creator>Oldcola</dc:creator>
				<category><![CDATA[Antoine&#039;s picks]]></category>

		<guid isPermaLink="false">https://portablegenomics.wordpress.com/?p=283</guid>
		<description><![CDATA[Maternal Plasma DNA Sequencing Reveals the Genome-Wide Genetic and Mutational Profile of the Fetus Y. M. D. Lo, K. C. A. Chan, H. Sun, E. Z. Chen, P. Jiang, F. M. F. Lun, Y. W. Zheng, T. Y. Leung, T. K. Lau, C. R. Cantor, R. W. K. Chiu Sci. Transl. Med. 2, 61ra91 (2010) [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=portablegenomics.wordpress.com&amp;blog=9871701&amp;post=283&amp;subd=portablegenomics&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
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		<slash:comments>0</slash:comments>
	
		<media:content url="http://1.gravatar.com/avatar/38061a8ce7125c778c0f114ae99f0ff5?s=96&#38;d=identicon&#38;r=G" medium="image">
			<media:title type="html">Oldcola</media:title>
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		<item>
		<title>Carrier Testing for Severe Childhood Recessive Diseases by Next-Generation Sequencing</title>
		<link>http://portablegenomics.wordpress.com/2011/01/16/carrier-testing-for-severe-childhood-recessive-diseases-by-next-generation-sequencing/</link>
		<comments>http://portablegenomics.wordpress.com/2011/01/16/carrier-testing-for-severe-childhood-recessive-diseases-by-next-generation-sequencing/#comments</comments>
		<pubDate>Sun, 16 Jan 2011 15:14:51 +0000</pubDate>
		<dc:creator>Oldcola</dc:creator>
				<category><![CDATA[Antoine&#039;s picks]]></category>

		<guid isPermaLink="false">https://portablegenomics.wordpress.com/?p=281</guid>
		<description><![CDATA[Carrier Testing for Severe Childhood Recessive Diseases by Next-Generation Sequencing C. J. Bell, D. L. Dinwiddie, N. A. Miller, S. L. Hateley, E. E. Ganusova, J. Mudge, R. J. Langley, L. Zhang, C. C. Lee, F. D. Schilkey, V. Sheth, J. E. Woodward, H. E. Peckham, G. P. Schroth, R. W. Kim, S. F. Kingsmore [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=portablegenomics.wordpress.com&amp;blog=9871701&amp;post=281&amp;subd=portablegenomics&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
		<wfw:commentRss>http://portablegenomics.wordpress.com/2011/01/16/carrier-testing-for-severe-childhood-recessive-diseases-by-next-generation-sequencing/feed/</wfw:commentRss>
		<slash:comments>0</slash:comments>
	
		<media:content url="http://1.gravatar.com/avatar/38061a8ce7125c778c0f114ae99f0ff5?s=96&#38;d=identicon&#38;r=G" medium="image">
			<media:title type="html">Oldcola</media:title>
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		<item>
		<title>Effect of Direct-to-Consumer Genomewide Profiling to Assess Disease Risk</title>
		<link>http://portablegenomics.wordpress.com/2011/01/13/effect-of-direct-to-consumer-genomewide-profiling-to-assess-disease-risk/</link>
		<comments>http://portablegenomics.wordpress.com/2011/01/13/effect-of-direct-to-consumer-genomewide-profiling-to-assess-disease-risk/#comments</comments>
		<pubDate>Thu, 13 Jan 2011 15:21:56 +0000</pubDate>
		<dc:creator>Oldcola</dc:creator>
				<category><![CDATA[Antoine&#039;s picks]]></category>

		<guid isPermaLink="false">https://portablegenomics.wordpress.com/?p=279</guid>
		<description><![CDATA[Effect of Direct-to-Consumer Genomewide Profiling to Assess Disease Risk Cinnamon S. Bloss, Ph.D., Nicholas J. Schork, Ph.D., and Eric J. Topol, M.D. doi:10.1056/NEJMoa1011893 was published on January 12, 2011, at NEJM Background The use of direct-to-consumer genomewide profiling to assess disease risk is controversial, and little is known about the effect of this technology on [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=portablegenomics.wordpress.com&amp;blog=9871701&amp;post=279&amp;subd=portablegenomics&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
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		<slash:comments>0</slash:comments>
	
		<media:content url="http://1.gravatar.com/avatar/38061a8ce7125c778c0f114ae99f0ff5?s=96&#38;d=identicon&#38;r=G" medium="image">
			<media:title type="html">Oldcola</media:title>
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		<item>
		<title>Genetic Link for Depression Furthered by Analysis of 54 Studies</title>
		<link>http://portablegenomics.wordpress.com/2011/01/07/genetic-link-for-depression-furthered-by-analysis-of-54-studies/</link>
		<comments>http://portablegenomics.wordpress.com/2011/01/07/genetic-link-for-depression-furthered-by-analysis-of-54-studies/#comments</comments>
		<pubDate>Fri, 07 Jan 2011 21:48:15 +0000</pubDate>
		<dc:creator>pmerel</dc:creator>
				<category><![CDATA[genomic medicine]]></category>
		<category><![CDATA[Patrick&#039;s picks]]></category>
		<category><![CDATA[depression]]></category>
		<category><![CDATA[medicine]]></category>
		<category><![CDATA[predictive]]></category>
		<category><![CDATA[serotonin]]></category>
		<category><![CDATA[suceptibility]]></category>
		<category><![CDATA[u-m]]></category>

		<guid isPermaLink="false">https://portablegenomics.wordpress.com/?p=277</guid>
		<description><![CDATA[Genetic Link for Depression Furthered by Analysis of 54 Studies: University of Michigan Health System researchers say that genes determine susceptibility to depression. Their findings challenge a 2009 study that called the genetic link into question and add support to previous research that revealed this link. &#8220;For their research the U-M team examined 54 studies [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=portablegenomics.wordpress.com&amp;blog=9871701&amp;post=277&amp;subd=portablegenomics&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
		<wfw:commentRss>http://portablegenomics.wordpress.com/2011/01/07/genetic-link-for-depression-furthered-by-analysis-of-54-studies/feed/</wfw:commentRss>
		<slash:comments>0</slash:comments>
	
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			<media:title type="html">pmerel</media:title>
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		<item>
		<title>Portable Genomics dans la presse: compléments d&#8217;information</title>
		<link>http://portablegenomics.wordpress.com/2011/01/01/portable-genomics-dans-la-presse-complements-dinformation/</link>
		<comments>http://portablegenomics.wordpress.com/2011/01/01/portable-genomics-dans-la-presse-complements-dinformation/#comments</comments>
		<pubDate>Sat, 01 Jan 2011 00:00:35 +0000</pubDate>
		<dc:creator>pmerel</dc:creator>
				<category><![CDATA[Antoine&#039;s picks]]></category>
		<category><![CDATA[genomic medicine]]></category>
		<category><![CDATA[Patrick&#039;s picks]]></category>
		<category><![CDATA[dtc-genomics]]></category>
		<category><![CDATA[genome]]></category>
		<category><![CDATA[genomic]]></category>
		<category><![CDATA[genomics]]></category>
		<category><![CDATA[genomique]]></category>
		<category><![CDATA[health 2.0]]></category>
		<category><![CDATA[medecine personalisee]]></category>
		<category><![CDATA[santé]]></category>
		<category><![CDATA[sequencing]]></category>
		<category><![CDATA[wireless healthcare]]></category>

		<guid isPermaLink="false">https://portablegenomics.wordpress.com/?p=254</guid>
		<description><![CDATA[Yves Eude signe un papier sur Portable Genomics paru dans Le Monde du 29 Décembre 2010. Nos remerciements publiques ici pour cette présentation de notre projet et pour le débat lancé sur des sujets comme génome et bioéthique, médecine 2.0, innovation et entrepreneuriat. Nous profitons de l&#8217;espace, plus disponible, du blog pour compléter cette enquête [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=portablegenomics.wordpress.com&amp;blog=9871701&amp;post=254&amp;subd=portablegenomics&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
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		<slash:comments>10</slash:comments>
	
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			<media:title type="html">pmerel</media:title>
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			<media:title type="html">PGexplicit.jpg</media:title>
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		<item>
		<title>DTC-Genomics Players List 2.0 &#8211; A collaborative table through SocialCompare.com</title>
		<link>http://portablegenomics.wordpress.com/2010/11/30/dtc-genomics-players-list-2-0-a-collaborative-table-through-socialcompare-com/</link>
		<comments>http://portablegenomics.wordpress.com/2010/11/30/dtc-genomics-players-list-2-0-a-collaborative-table-through-socialcompare-com/#comments</comments>
		<pubDate>Tue, 30 Nov 2010 10:54:38 +0000</pubDate>
		<dc:creator>pmerel</dc:creator>
				<category><![CDATA[Patrick&#039;s picks]]></category>
		<category><![CDATA[ancestry]]></category>
		<category><![CDATA[dtc-genomics]]></category>
		<category><![CDATA[genetic]]></category>
		<category><![CDATA[genome]]></category>
		<category><![CDATA[genomic]]></category>
		<category><![CDATA[health]]></category>
		<category><![CDATA[healthcare 2.0]]></category>
		<category><![CDATA[social]]></category>
		<category><![CDATA[test]]></category>

		<guid isPermaLink="false">https://portablegenomics.wordpress.com/?p=245</guid>
		<description><![CDATA[We have created a collaborative table, thanxx to SocialCompare, trying to bring a full list of the players in the field of Direct-to-Consumer Genomics. SocialCompare allows you to participate into this effort, make any correction if needed, rate and tell everyone if you like the company&#8217;s service. Let&#8217;s try Genomics 2.0. Table is here. (URL: http://socialcompare.com/en/w/dtc-genomics-players-gfy0dlz) [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=portablegenomics.wordpress.com&amp;blog=9871701&amp;post=245&amp;subd=portablegenomics&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
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		<slash:comments>1</slash:comments>
	
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			<media:title type="html">pmerel</media:title>
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		<title>Canadian scientists discover pattern of DNA mutation in 40 diseases</title>
		<link>http://portablegenomics.wordpress.com/2010/08/18/canadian-scientists-discover-pattern-of-dna-mutation-in-40-diseases/</link>
		<comments>http://portablegenomics.wordpress.com/2010/08/18/canadian-scientists-discover-pattern-of-dna-mutation-in-40-diseases/#comments</comments>
		<pubDate>Wed, 18 Aug 2010 13:43:02 +0000</pubDate>
		<dc:creator>pmerel</dc:creator>
				<category><![CDATA[Patrick&#039;s picks]]></category>
		<category><![CDATA[medicine]]></category>

		<guid isPermaLink="false">https://portablegenomics.wordpress.com/?p=241</guid>
		<description><![CDATA[A team of investigators at Sick Kids Hospital in Toronto (Christopher Pearson, lead researcher and senior scientist) collaborated with doctors in Paris, in a six-year international study that closely examined how progressive diseases rapidly develop in victims. &#8220;&#8230;Pearson&#8217;s findings, published Sunday in the scientific journal Nature Structural and Molecular Biology, are also the first to [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=portablegenomics.wordpress.com&amp;blog=9871701&amp;post=241&amp;subd=portablegenomics&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
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		<slash:comments>0</slash:comments>
	
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			<media:title type="html">pmerel</media:title>
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