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    <title>microarray at Yahoo! Groups</title>
    <link>http://tech.groups.yahoo.com/group/microarray/</link>
    <description>micro &amp; macro arrays</description>

    <item>
      <title>Re: Experiment design</title>
      <pubDate>Wed, 04 Nov 2009 09:04:00 GMT</pubDate>
      <dc:creator>Neil Graham</dc:creator>
      <link>http://tech.groups.yahoo.com/group/microarray/message/19890</link>
      <guid isPermaLink="true">http://tech.groups.yahoo.com/group/microarray/message/19890</guid>
      <description>Dear Muhammad, The experimental design looks fine and having 3 biological should be ok. With the 1 time point issue, I would recommend making sure that the </description>
    </item>
    <item>
      <title>Re: Experiment design</title>
      <pubDate>Wed, 04 Nov 2009 09:03:56 GMT</pubDate>
      <dc:creator>Luigi Marchionni</dc:creator>
      <link>http://tech.groups.yahoo.com/group/microarray/message/19889</link>
      <guid isPermaLink="true">http://tech.groups.yahoo.com/group/microarray/message/19889</guid>
      <description>you need to specify, platform, color scheme, and the like, otherwise it will be impossible to answer. Luigi Marchionni ... [Non-text portions of this message</description>
    </item>
    <item>
      <title>Re: Experiment design</title>
      <pubDate>Wed, 04 Nov 2009 09:03:13 GMT</pubDate>
      <dc:creator>sadia saeed</dc:creator>
      <link>http://tech.groups.yahoo.com/group/microarray/message/19888</link>
      <guid isPermaLink="true">http://tech.groups.yahoo.com/group/microarray/message/19888</guid>
      <description>Hello Javid, I am sorry, i cannot comment on your design as it is not my field. But nice to see a muslim guy here. Regards, Sadia ... From: javid_mirza</description>
    </item>
    <item>
      <title>Re: Experiment design</title>
      <pubDate>Tue, 03 Nov 2009 14:58:28 GMT</pubDate>
      <dc:creator>Agnieszka Lichanska</dc:creator>
      <link>http://tech.groups.yahoo.com/group/microarray/message/19887</link>
      <guid isPermaLink="true">http://tech.groups.yahoo.com/group/microarray/message/19887</guid>
      <description>Hi Muhammad, single time point has to be compared to some sort of baseline, untreated plants/leaves will be the most obvious choice as a baseline. Also an</description>
    </item>
    <item>
      <title>Re: Experiment design</title>
      <pubDate>Tue, 03 Nov 2009 14:57:46 GMT</pubDate>
      <dc:creator>crosbyseth</dc:creator>
      <link>http://tech.groups.yahoo.com/group/microarray/message/19886</link>
      <guid isPermaLink="true">http://tech.groups.yahoo.com/group/microarray/message/19886</guid>
      <description>Hello Muhammad, Statistically speaking, the experiment is fine as long as it addresses your hypothesis.  You could possibly find, after looking at the data,</description>
    </item>
    <item>
      <title>Re: Gene expression differences and fold change interpretation</title>
      <pubDate>Mon, 02 Nov 2009 12:23:56 GMT</pubDate>
      <dc:creator>Chris Seidel</dc:creator>
      <link>http://tech.groups.yahoo.com/group/microarray/message/19885</link>
      <guid isPermaLink="true">http://tech.groups.yahoo.com/group/microarray/message/19885</guid>
      <description>Hi Mervi, ... The fold-change, and the scale used to plot changes are usually different things. When people discuss fold-change, they do so in linear space, so</description>
    </item>
    <item>
      <title>Experiment design</title>
      <pubDate>Mon, 02 Nov 2009 12:19:11 GMT</pubDate>
      <dc:creator>javid_mirza</dc:creator>
      <link>http://tech.groups.yahoo.com/group/microarray/message/19884</link>
      <guid isPermaLink="true">http://tech.groups.yahoo.com/group/microarray/message/19884</guid>
      <description>Hi Fellows, I&#39;m starting RNA extractions from stressed leaves for microarray work with following parameters in mind Genotype= 1 Time point= 1 (4 weeks after</description>
    </item>
    <item>
      <title>LIMS swap program</title>
      <pubDate>Fri, 30 Oct 2009 09:14:34 GMT</pubDate>
      <dc:creator>Manoj</dc:creator>
      <link>http://tech.groups.yahoo.com/group/microarray/message/19883</link>
      <guid isPermaLink="true">http://tech.groups.yahoo.com/group/microarray/message/19883</guid>
      <description>I thought of passing this around to see if there are any such needs at your lab. Please feel free to pass this around to others whom you think might benefit</description>
    </item>
    <item>
      <title>International qPCR 2010 Symposium &amp; Exhibition in Vienna</title>
      <pubDate>Mon, 26 Oct 2009 09:34:43 GMT</pubDate>
      <dc:creator>genequantification</dc:creator>
      <link>http://tech.groups.yahoo.com/group/microarray/message/19882</link>
      <guid isPermaLink="true">http://tech.groups.yahoo.com/group/microarray/message/19882</guid>
      <description>International qPCR 2010 Symposium &amp; Exhibition in Vienna 7th ? 9th April 2010 The focus of the qPCR 2010 Event will be &quot;The ongoing evolution of qPCR&quot; Our</description>
    </item>
    <item>
      <title>Gene expression differences and fold change interpretation</title>
      <pubDate>Mon, 26 Oct 2009 08:40:41 GMT</pubDate>
      <dc:creator>Seth Crosby</dc:creator>
      <link>http://tech.groups.yahoo.com/group/microarray/message/19881</link>
      <guid isPermaLink="true">http://tech.groups.yahoo.com/group/microarray/message/19881</guid>
      <description>Illumina claims with the HT-12 you can believe down to a 1.3-fold change with a p-value of 0.01. The reason we log transform (and, by the way, it is usually</description>
    </item>
    <item>
      <title>Next Gen Sequencing Lab posts</title>
      <pubDate>Mon, 26 Oct 2009 08:40:03 GMT</pubDate>
      <dc:creator>Ian McFarlane</dc:creator>
      <link>http://tech.groups.yahoo.com/group/microarray/message/19880</link>
      <guid isPermaLink="true">http://tech.groups.yahoo.com/group/microarray/message/19880</guid>
      <description>Hi, We have three open positions in Cambridge (UK) for lab staff to run our complement of 5 next-gen sequencers (3xSOLiD, 1x454, 1xIllumina). The lab also</description>
    </item>
    <item>
      <title>Gene expression differences and fold change interpretation</title>
      <pubDate>Fri, 23 Oct 2009 17:26:40 GMT</pubDate>
      <dc:creator>smurffi03</dc:creator>
      <link>http://tech.groups.yahoo.com/group/microarray/message/19879</link>
      <guid isPermaLink="true">http://tech.groups.yahoo.com/group/microarray/message/19879</guid>
      <description>Dear All, I&#39;m analysing a pilot study with Illumina HT-12 data. I want to find differentially expressed genes but I&#39;m struggling with the interpretation of</description>
    </item>
    <item>
      <title>a survey from the Jackson Laboratory</title>
      <pubDate>Fri, 09 Oct 2009 07:35:21 GMT</pubDate>
      <dc:creator>Eric Antoniou</dc:creator>
      <link>http://tech.groups.yahoo.com/group/microarray/message/19878</link>
      <guid isPermaLink="true">http://tech.groups.yahoo.com/group/microarray/message/19878</guid>
      <description>Dear Colleagues The Jackson Laboratory gene expression and Next Generation Sequencing core laboratory is doing a survey of comparable core labs to benchmark</description>
    </item>
    <item>
      <title>Re: metatranscriptome</title>
      <pubDate>Mon, 05 Oct 2009 07:30:16 GMT</pubDate>
      <dc:creator>crosbyseth</dc:creator>
      <link>http://tech.groups.yahoo.com/group/microarray/message/19877</link>
      <guid isPermaLink="true">http://tech.groups.yahoo.com/group/microarray/message/19877</guid>
      <description>There are many platforms and many arrays which already exist which you could buy tomorrow.  What species?</description>
    </item>
    <item>
      <title>Re: Real time PCR machines</title>
      <pubDate>Fri, 02 Oct 2009 08:35:03 GMT</pubDate>
      <dc:creator>saifmunshi</dc:creator>
      <link>http://tech.groups.yahoo.com/group/microarray/message/19876</link>
      <guid isPermaLink="true">http://tech.groups.yahoo.com/group/microarray/message/19876</guid>
      <description>Hi All We are planning to buy a real Time PCR within 20000 USD which should have at least 96 wells . We prefer ABI, Bio Rad . IS it possible ?? -Saif</description>
    </item>

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