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    <title>Genorama news</title>
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    <link>http://www.genorama.com/</link>
    <description>Latest News</description>
    <language>en-en</language>
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    <item>
      <title><![CDATA[ Animation - DNA analysis with APEX technology ]]></title>
      <link>http://www.genorama.com/EN/about-genorama/blog/dna-analysis-with-apex-technology/?utm_source=rss&amp;utm_medium=feed&amp;utm_campaign=Feed%3A+GenoramaNews+(Genorama+News)</link>
      <pubDate>Mon, 11 Mar 2013 00:00:00 +0200</pubDate>
      <guid isPermaLink="true">genorama73</guid>
      <description><![CDATA[ Have you ever wondered how is it possible to acquire data from the DNAs? Now you can see how it’s done with the help of the APEX technology. From https://www.youtube.com/watch?v=SDJDucBsmdA you’ll see the whole process animated in 3D. ]]></description>
    </item>
    <item>
      <title><![CDATA[ APEX Training kit for 10 reactions now launched ]]></title>
      <link>http://www.genorama.com/EN/about-genorama/blog/apex-training-kit-for-10-reactions-now-launched/?utm_source=rss&amp;utm_medium=feed&amp;utm_campaign=Feed%3A+GenoramaNews+(Genorama+News)</link>
      <pubDate>Mon, 05 Nov 2012 00:00:00 +0200</pubDate>
      <guid isPermaLink="true">genorama72</guid>
      <description><![CDATA[ You have stored the DNA and ordered the analysis kits for your experiments but you feel a bit uncertain as the amount of DNA is rather limited and you just can not afford wasting any drops of that valuable material. In case this situation is familiar then perhaps one solution could be our new product - the APEX Training Kit. ]]></description>
    </item>
    <item>
      <title><![CDATA[ Validated Genorama APEX-technology has its niche in the diagnostic lab along with NGS platforms ]]></title>
      <link>http://www.genorama.com/EN/about-genorama/blog/validated-microarray-based-genorama-apex-technology-has-its-niche-in-the-diagnostic-lab/?utm_source=rss&amp;utm_medium=feed&amp;utm_campaign=Feed%3A+GenoramaNews+(Genorama+News)</link>
      <pubDate>Mon, 01 Oct 2012 00:00:00 +0200</pubDate>
      <guid isPermaLink="true">genorama71</guid>
      <description><![CDATA[ Compiled by Hanno Roomere, M.Sc. 

As the efforts in reducing cost for Next Generation Sequencing (NGS) platforms has led to a situation where more and more laboratories have reached to the stage where they can allow themselves to acquire one, it has led us to compile this post to offer a few ideas of how one could benefit from merging both technologies. ]]></description>
    </item>
    <item>
      <title><![CDATA[ What is the difference between APEX Template Preparation Kit and APEX Reaction Mixture Kit ]]></title>
      <link>http://www.genorama.com/EN/about-genorama/blog/what-is-the-difference-between-apex-template-preparation-kit-and-apex-reaction-mixture-kit/?utm_source=rss&amp;utm_medium=feed&amp;utm_campaign=Feed%3A+GenoramaNews+(Genorama+News)</link>
      <pubDate>Mon, 24 Sep 2012 00:00:00 +0200</pubDate>
      <guid isPermaLink="true">genorama70</guid>
      <description><![CDATA[ In case the structure of our analysis kits was a bit difficult to understand then to make it easier to follow, we assembled our kits in a way that all the components would be named in a way that there would be no confusion. ]]></description>
    </item>
    <item>
      <title><![CDATA[ Hereditary Hearing Loss and  ABCA4 gene (Stargardt disease) analysis projects updated ]]></title>
      <link>http://www.genorama.com/EN/about-genorama/blog/hereditary-hearing-loss-and--abca4-gene-stargardt-disease-analysis-projects-updated/?utm_source=rss&amp;utm_medium=feed&amp;utm_campaign=Feed%3A+GenoramaNews+(Genorama+News)</link>
      <pubDate>Mon, 17 Sep 2012 00:00:00 +0200</pubDate>
      <guid isPermaLink="true">genorama69</guid>
      <description><![CDATA[ We would like to announce of two updates in our projects. One of the 
updated tests is our well welcomed Hereditary Hearing Loss test that now 
covers 249 mutations from 11 genes. And the other one is Stargardt 
disease test that now covers 632 mutations from ABCR4 gene. ]]></description>
    </item>
    <item>
      <title><![CDATA[ Ashkenazi Jewish Diseases project updated with USH3A from Usher Syndrome, type IIIA ]]></title>
      <link>http://www.genorama.com/EN/about-genorama/blog/ashkenazi-jewish-diseases-project-updated2/?utm_source=rss&amp;utm_medium=feed&amp;utm_campaign=Feed%3A+GenoramaNews+(Genorama+News)</link>
      <pubDate>Mon, 13 Aug 2012 00:00:00 +0200</pubDate>
      <guid isPermaLink="true">genorama68</guid>
      <description><![CDATA[ Genorama is pleased to announce of another update in Ashkenazi Jewish Diseases project. The Ashkenazi Jewish Diseases test now allows to detect the mutation USH3A from Usher Syndrome, type IIIA. Combined with the former variants it now enables to analyse 108 mutations from 24 genes. ]]></description>
    </item>
    <item>
      <title><![CDATA[ Microarrays for other species than human ]]></title>
      <link>http://www.genorama.com/EN/about-genorama/blog/microarrays-for-other-species-than-human/?utm_source=rss&amp;utm_medium=feed&amp;utm_campaign=Feed%3A+GenoramaNews+(Genorama+News)</link>
      <pubDate>Mon, 23 Jul 2012 00:00:00 +0200</pubDate>
      <guid isPermaLink="true">genorama67</guid>
      <description><![CDATA[ Can you spot microarrays for other species than human? To cut the long story short - yes, we can. And to stall it slightly longer again then it must be added that only for species for which the whole genome has been sequenced. ]]></description>
    </item>
    <item>
      <title><![CDATA[ Custom spotting service ]]></title>
      <link>http://www.genorama.com/EN/about-genorama/blog/custom-spotting-service/?utm_source=rss&amp;utm_medium=feed&amp;utm_campaign=Feed%3A+GenoramaNews+(Genorama+News)</link>
      <pubDate>Mon, 16 Jul 2012 00:00:00 +0200</pubDate>
      <guid isPermaLink="true">genorama66</guid>
      <description><![CDATA[ Over the years we have received several questions about custom spotted slides. The questions have varied from simple whether-you-still-do-it to more detailed do-you-provide-your-own-oligos and a large variety that fit between the above mentioned.
To the ones of you who are interested in the first one the simple answer is – yes, we are still doing it. And for the ones interested in the last one – yes, we do.
The information one has to consider whilst planning custom spotting service can be summoned up in following paragraphs. ]]></description>
    </item>
    <item>
      <title><![CDATA[ Autosomal Dominant Optic Atrophy analysis project updated ]]></title>
      <link>http://www.genorama.com/EN/about-genorama/blog/autosomal-dominant-optic-atrophy-analysis-project-updated/?utm_source=rss&amp;utm_medium=feed&amp;utm_campaign=Feed%3A+GenoramaNews+(Genorama+News)</link>
      <pubDate>Tue, 03 Apr 2012 00:00:00 +0200</pubDate>
      <guid isPermaLink="true">genorama65</guid>
      <description><![CDATA[ Two more genetic variations were added to Genorama’s Autosomal Dominant Optic Atrophy (ADOA) analysis project that makes the total number of genetic variations associated with the ADOA to 120. Please click <a href="http://www.genorama.com/EN/products/genetic-tests/autosomal-dominant-optic-atrophy-analysis-kit/" target="_blank">here</a> for more information. ]]></description>
    </item>
    <item>
      <title><![CDATA[ ABCA4 gene (Stargardt disease) analysis project updated ]]></title>
      <link>http://www.genorama.com/EN/about-genorama/blog/abca4-gene-stargardt-disease-analysis-project-updated/?utm_source=rss&amp;utm_medium=feed&amp;utm_campaign=Feed%3A+GenoramaNews+(Genorama+News)</link>
      <pubDate>Mon, 02 Apr 2012 00:00:00 +0200</pubDate>
      <guid isPermaLink="true">genorama64</guid>
      <description><![CDATA[ Genorama is pleased to announce of an update of ABCR4 gene (Stargardt
disease related) project. The test now allows detecting 72 more
genetic variations that makes the total number of genetic variations associated to Stargardt
disease 630. Please click <a href="http://www.genorama.com/EN/products/genetic-tests/abca4-gene-%28stargardt%29-analysis-kit/" target="_blank">here</a> for more information.  ]]></description>
    </item>
    <item>
      <title><![CDATA[ Ashkenazi Jewish Diseases project updated ]]></title>
      <link>http://www.genorama.com/EN/about-genorama/blog/ashkenazi-jewish-diseases-project-updated/?utm_source=rss&amp;utm_medium=feed&amp;utm_campaign=Feed%3A+GenoramaNews+(Genorama+News)</link>
      <pubDate>Wed, 12 Oct 2011 00:00:00 +0200</pubDate>
      <guid isPermaLink="true">genorama63</guid>
      <description><![CDATA[ Genorama is pleased to announce of an update of Ashkenazi Jewish Diseases project. The Ashkenazi Jewish Diseases test now allows to detect the Joubert Syndrome 2 related c.35G>T or c.218G>T mutation in gene's TMEM216 third exon. Please click here for further information. ]]></description>
    </item>
    <item>
      <title><![CDATA[ IVD CE certification issued to Genorama Cystic Fibrosis Analysis KIT ]]></title>
      <link>http://www.genorama.com/EN/about-genorama/blog/ivd-ce-certification-issued-to-genorama-cystic-fibrosis-analysis-kit/?utm_source=rss&amp;utm_medium=feed&amp;utm_campaign=Feed%3A+GenoramaNews+(Genorama+News)</link>
      <pubDate>Wed, 20 Apr 2011 00:00:00 +0200</pubDate>
      <guid isPermaLink="true">genorama62</guid>
      <description><![CDATA[ Genorama is pleased to announce of an IVD CE certificate issued to Cystic Fibrosis Analysis KIT. The kit enables to analyse  271 Cystic Fibrosis genetic variations from CFTR gene and it represents the most frequently screened mutations in both Caucasians as well as non-Caucasians populations. Click <a href="http://www.genorama.com/EN/products/ivd-genetic-tests/cystic-fibrosis-analysis-kit/" target="_blank">here</a> for more information. ]]></description>
    </item>
    <item>
      <title><![CDATA[ IVD CE marked Thalassamia testing panel launched ]]></title>
      <link>http://www.genorama.com/EN/about-genorama/blog/ivd-ce-marked-thalassamia-testing-panel-launched/?utm_source=rss&amp;utm_medium=feed&amp;utm_campaign=Feed%3A+GenoramaNews+(Genorama+News)</link>
      <pubDate>Mon, 03 Jan 2011 00:00:00 +0200</pubDate>
      <guid isPermaLink="true">genorama57</guid>
      <description><![CDATA[ Genorama has been working on Thalassemia testing since 2008 and now the comprehensive kit for testing of 69 mutations has been approved as IVD CE certified diagnostics kit. Click <a href="http://www.genorama.com/EN/products/ivd-genetic-tests/beta-thalassemia-analysis-kit/" target="_blank">here</a> for more information. ]]></description>
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