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      <DESIGN_DESCRIPTION>DNA extraction was conducted utilizing the enhanced CTAB method. Following this, the quality of the extracted DNA was assessed through 0.8% agarose gel electrophoresis, and quantified using a UV spectrophotometer. Subsequently, a library comprising 400 bp insert fragments was constructed on the Illumina Novaseq platform, followed by paired-end sequencing to acquire 150 bp sequences from both ends of every read.</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
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        <LIBRARY_SELECTION>repeat fractionation</LIBRARY_SELECTION>
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          <PAIRED/>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
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        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
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        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
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        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
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      <DESIGN_DESCRIPTION>DNA extraction was conducted utilizing the enhanced CTAB method. Following this, the quality of the extracted DNA was assessed through 0.8% agarose gel electrophoresis, and quantified using a UV spectrophotometer. Subsequently, a library comprising 400 bp insert fragments was constructed on the Illumina Novaseq platform, followed by paired-end sequencing to acquire 150 bp sequences from both ends of every read.</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
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      <DESIGN_DESCRIPTION>DNA extraction was conducted utilizing the enhanced CTAB method. Following this, the quality of the extracted DNA was assessed through 0.8% agarose gel electrophoresis, and quantified using a UV spectrophotometer. Subsequently, a library comprising 400 bp insert fragments was constructed on the Illumina Novaseq platform, followed by paired-end sequencing to acquire 150 bp sequences from both ends of every read.</DESIGN_DESCRIPTION>
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