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      <source-app name="Horizon">Horizon</source-app>
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      <ref-type name="Journal Article">17</ref-type>
      <work-type>ACL : Articles dans des revues avec comité de lecture répertoriées par l'AERES</work-type>
      <contributors>
        <authors>
          <author>
            <style face="normal" font="default" size="100%">Carrier, G.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Santoni, S.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Rodier-Goud, M.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Canaguier, A.</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Kochko, Alexandre de</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Tranchant Dubreuil, Christine</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">This, P.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Boursiquot, J.M.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Le Cunff, L.</style>
          </author>
        </authors>
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      <titles>
        <title>An efficient and rapid protocol for plant nuclear DNA preparation suitable for next generation sequencing methods</title>
        <secondary-title>American Journal of Botany</secondary-title>
      </titles>
      <pages>E13-E15</pages>
      <keywords>
        <keyword>next generation sequencers</keyword>
        <keyword>nuclear plant DNA extraction</keyword>
        <keyword>nuclei</keyword>
        <keyword>isolation</keyword>
      </keywords>
      <dates>
        <year>2011</year>
      </dates>
      <call-num>fdi:010053128</call-num>
      <language>ENG</language>
      <periodical>
        <full-title>American Journal of Botany</full-title>
      </periodical>
      <isbn>0002-9122</isbn>
      <accession-num>ISI:000285747900005</accession-num>
      <number>1</number>
      <electronic-resource-num>10.3732/ajb.1000371</electronic-resource-num>
      <urls>
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          <url>https://www.documentation.ird.fr/hor/fdi:010053128</url>
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          <url>https://www.documentation.ird.fr/intranet/publi/2011/03/010053128.pdf</url>
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      <volume>98</volume>
      <remote-database-provider>Horizon (IRD)</remote-database-provider>
      <abstract>Premise of the study : In this study, we developed a nuclear DNA extraction protocol for Next Generation Sequencers (NGS). Methods and Results : We applied this extraction method to grapevines and coffee trees, which are known to contain many secondary metabolites. The nuclear DNA obtained was sequenced by the 454/GS-FLX method. We obtained excellent results, with less than 4% cytoplasmic DNA, in a similar way to a BAC (Bacterial Artificial Chromosome)-building protocol. We also compared our protocol with a classic DNA extraction using specific cytoplasmic DNA amplification. Results showed a lower cytoplasmic DNA contamination with the new protocol. Conclusions : The method presented here is fast and economical. The DNA obtained is of high quality, with a low level of cytoplasmic DNA contamination, and very efficient for the construction of sequencing libraries.</abstract>
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      <custom1>UR188</custom1>
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