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    <titleInfo>
      <title>An efficient and rapid protocol for plant nuclear DNA preparation suitable for next generation sequencing methods</title>
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    <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>
    <targetAudience authority="marctarget">specialized</targetAudience>
    <subject>
      <topic>next generation sequencers</topic>
      <topic>nuclear plant DNA extraction</topic>
      <topic>nuclei</topic>
      <topic>isolation</topic>
    </subject>
    <classification authority="local">076</classification>
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      <titleInfo>
        <title>American Journal of Botany</title>
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      <part>
        <detail type="volume">
          <number>98</number>
        </detail>
        <detail type="volume">
          <number>1</number>
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        <extent unit="pages">
          <list> E13-E15</list>
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      <originInfo>
        <dateIssued>2011</dateIssued>
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      <identifier type="issn">0002-9122</identifier>
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    <identifier type="uri">https://www.documentation.ird.fr/hor/fdi:010053128</identifier>
    <identifier type="doi">10.3732/ajb.1000371</identifier>
    <identifier type="issn">0002-9122</identifier>
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      <recordCreationDate encoding="w3cdtf">2011-04-07</recordCreationDate>
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