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   <ui>gb-spotlight-20010411-01</ui>
   <ji>GBJ</ji>
   <fm>
      <dochead>Research news</dochead>
      <bibl>
         <title>
            <p>Second-generation microarrays</p>
         </title>
         <aug>
            <au id="A1">
               <snm>Weitzman</snm>
               <mi>B</mi>
               <fnm>Jonathan</fnm>
               <email>jonathanweitzman@hotmail.com</email>
            </au>
         </aug>
         <source>Genome Biology</source>
         <issn>1465-6906</issn>
         <pubdate>2001</pubdate>
         <volume>2</volume>
         <fpage>spotlight-20010411-01</fpage>
         <xrefbib>
            <pubid idtype="doi">10.1186/gb-spotlight-20010411-01</pubid>
         </xrefbib>
      </bibl>
      <history>
         <pub>
            <date>
               <day>11</day>
               <month>04</month>
               <year>2001</year>
            </date>
         </pub>
      </history>
      <cpyrt>
         <year>2001</year>
         <collab>BioMed Central Ltd</collab>
      </cpyrt>
      <shortabs>
         <p>Ink-jet oligonucleotide microarray technology offers a flexible system for gene expression profiling.</p>
      </shortabs>
   </fm>
   <meta>
      <classifications>
         <classification type="STATUS">Archive</classification>
      </classifications>
   </meta>
   <bdy>
      <sec>
         <st>
            <p/>
         </st>
         <p>Current microarray analysis uses 'chips' containing either 25-residue <abbr bid="B1">oligonucleotides</abbr> synthesized by photolithography or <abbr bid="B2">cDNAs</abbr> placed by robotic spotting. In the April <abbr bid="B3"><it>Nature Biotechnology</it></abbr>, Hughes <it>et al</it>. describe a microarray technique that exploits an ink-jet printing method and standard phosphoramidite chemistry (<it>Nature Biotechnology</it> 2001, <b>19:</b>342-347). The ink-jet synthesizer can deliver 25,000 phosphoramidite-containing microdroplets to a 25 x 75 mm glass slide. Hughes <it>et al</it>. examined a large range of parameters to define conditions for optimized specificity and sensitivity. They found that 60-mer oligonucleotides hybridized at 30-32% formamide gave the best results. The absolute detection limit was approximately 0.1 copies per cell equivalent. The ink-jet arrays were as effective as spotted cDNA microarrays. Moreover, Hughes <it>et al</it>. report that single carefully chosen 60-mer oligonucleotides can be preferable to arrays containing multiple oligonucleotides or cDNAs as they offer maximal specificity. The ink-jet technology provides a very <abbr bid="B4">flexible microarray</abbr> system that can be experimentally optimized to detect low abundance mRNAs and spliced variants.</p>
      </sec>
   </bdy>
   <bm>
      <refgrp>
         <bibl id="B1">
            <note>Expression monitoring by hybridization to high-density oligonucleotide arrays.</note>
            <xrefbib>
               <pubid idtype="pmpid">9634850</pubid>
            </xrefbib>
         </bibl>
         <bibl id="B2">
            <note>Quantitative monitoring of gene expression patterns with a complementary DNA microarray.</note>
            <xrefbib>
               <pubid idtype="pmpid">7569999</pubid>
            </xrefbib>
         </bibl>
         <bibl id="B3">
            <url>http://biotech.nature.com</url>
            <note>
               <it>Nature Biotechnology</it>
            </note>
         </bibl>
         <bibl id="B4">
            <note>Experimental annotation of the human genome using microarray technology.</note>
            <xrefbib>
               <pubid idtype="pmpid" link="fulltext">11237012</pubid>
            </xrefbib>
         </bibl>
      </refgrp>
   </bm>
</art>
