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   <ui>gb-spotlight-20020115-01</ui>
   <ji>GBJ</ji>
   <fm>
      <dochead>Research news</dochead>
      <bibl>
         <title>
            <p>Finding the bug in the system</p>
         </title>
         <aug>
            <au id="A1">
               <snm>Toma</snm>
               <fnm>Tudor</fnm>
               <email>t.toma@ic.ac.uk</email>
            </au>
         </aug>
         <source>Genome Biology</source>
         <issn>1465-6906</issn>
         <pubdate>2002</pubdate>
         <volume>3</volume>
         <fpage>spotlight-20020115-01</fpage>
         <xrefbib>
            <pubid idtype="doi">10.1186/gb-spotlight-20020115-01</pubid>
         </xrefbib>
      </bibl>
      <history>
         <pub>
            <date>
               <day>15</day>
               <month>01</month>
               <year>2002</year>
            </date>
         </pub>
      </history>
      <cpyrt>
         <year>2002</year>
         <collab>BioMed Central Ltd</collab>
      </cpyrt>
      <shortabs>
         <p>Computational subtraction uses the human genome to detect possible microbial causes for infectious diseases.</p>
      </shortabs>
   </fm>
   <meta>
      <classifications>
         <classification type="STATUS">Archive</classification>
      </classifications>
   </meta>
   <bdy>
      <sec>
         <st>
            <p/>
         </st>
         <p>After <it>Helicobacter pylori</it> was implicated in the development of peptic ulcers, other common diseases - such as asthma and atherosclerosis - were screened for known and unknown pathogens, but the available detection methods failed to reveal causative microorganisms. In the January 14 online issue of <abbr bid="B1"><it>Nature Genetics</it></abbr>, Griffin Weber and colleagues from <abbr bid="B2">Dana-Farber Cancer Institute</abbr>, Boston, Massachusetts, USA describe a novel method to detect microbial causes behind infectious diseases by sequence transcript filtering against the human genome.</p>
         <p>Weber <it>et al.</it> developed an <it>in silico</it> approach that employed the draft sequence of the human genome to identify nonhuman DNA sequences in expressed-sequence tag (EST) libraries of human origin. Using this method (called computational subtraction) they identified known viral pathogens such as HPV-18 in cervical carcinoma tissues (<it>Nat Genet</it> 2002, DOI: 10.1038/ng818).</p>
         <p>"We therefore propose to generate, sequence and filter cDNA libraries from tissues of diseases such as systemic lupus erythematosus and extraintestinal Crohn disease, which are candidates for infectious etiology. [...] Further experiments could then distinguish sequences of benign commensal organisms from pathogen sequences by assessing the strength of their association with disease", concluded the authors.</p>
      </sec>
   </bdy>
   <bm>
      <refgrp>
         <bibl id="B1">
            <url>http://genetics.nature.com </url>
            <note>Weber G, Shendure J, Tanenbaum DM, Church GM, Meyerson M: <b>Identification of foreign gene sequences by transcript filtering against the human genome. </b><it>Nat Genet</it> 2002, DOI: 10.1038/ng818.</note>
         </bibl>
         <bibl id="B2">
            <url>http://www.dana-farber.org/ </url>
            <note>Dana-Farber Cancer Institute</note>
         </bibl>
      </refgrp>
   </bm>
</art>
