<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX11049079" alias="FA_16S">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX11049079</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9777487">FA_16S</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Nanopore sequencing of gut symbionts in Coptotermes heimi</TITLE>
    <STUDY_REF accession="SRP322334">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP322334</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9777487">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Library was prepared using barcoding of PCR amplified products. Basecalling and demultiplexing of Fast5 sequencing reads was done using Guppy program. Next, only high quality reads (q&gt;10) were filtered using using NanoFilt.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS9117113">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS9117113</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|manishagupta293@gmail.com">FA_16S</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>FA_16S</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <OXFORD_NANOPORE>
        <INSTRUMENT_MODEL>MinION</INSTRUMENT_MODEL>
      </OXFORD_NANOPORE>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX11049080" alias="MA_16S">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX11049080</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9777487">MA_16S</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Nanopore sequencing of gut symbionts in Coptotermes heimi</TITLE>
    <STUDY_REF accession="SRP322334">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP322334</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9777487">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Library was prepared using barcoding of PCR amplified products. Basecalling and demultiplexing of Fast5 sequencing reads was done using Guppy program. Next, only high quality reads (q&gt;10) were filtered using using NanoFilt.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS9117114">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS9117114</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|manishagupta293@gmail.com">MA_16S</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>MA_16S</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <OXFORD_NANOPORE>
        <INSTRUMENT_MODEL>MinION</INSTRUMENT_MODEL>
      </OXFORD_NANOPORE>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX11049081" alias="ISW_Protist">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX11049081</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9777487">ISW_Protist</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Nanopore sequencing of gut symbionts in Coptotermes heimi</TITLE>
    <STUDY_REF accession="SRP322334">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP322334</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9777487">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Library was prepared using barcoding of PCR amplified products. Basecalling and demultiplexing of Fast5 sequencing reads was done using Guppy program. Next, only high quality reads (q&gt;10) were filtered using using NanoFilt.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS9117115">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS9117115</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|manishagupta293@gmail.com">ISW_Protist</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>ISW_Protist</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <OXFORD_NANOPORE>
        <INSTRUMENT_MODEL>MinION</INSTRUMENT_MODEL>
      </OXFORD_NANOPORE>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX11049082" alias="FW_Protist">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX11049082</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9777487">FW_Protist</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Nanopore sequencing of gut symbionts in Coptotermes heimi</TITLE>
    <STUDY_REF accession="SRP322334">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP322334</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9777487">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Library was prepared using barcoding of PCR amplified products. Basecalling and demultiplexing of Fast5 sequencing reads was done using Guppy program. Next, only high quality reads (q&gt;10) were filtered using using NanoFilt.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS9117116">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS9117116</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|manishagupta293@gmail.com">FW_Protist</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>FW_Protist</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <OXFORD_NANOPORE>
        <INSTRUMENT_MODEL>MinION</INSTRUMENT_MODEL>
      </OXFORD_NANOPORE>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX11049083" alias="ISW_16S">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX11049083</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9777487">ISW_16S</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Nanopore sequencing of gut symbionts in Coptotermes heimi</TITLE>
    <STUDY_REF accession="SRP322334">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP322334</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9777487">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Library was prepared using barcoding of PCR amplified products. Basecalling and demultiplexing of Fast5 sequencing reads was done using Guppy program. Next, only high quality reads (q&gt;10) were filtered using using NanoFilt.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS9117117">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS9117117</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|manishagupta293@gmail.com">ISW_16S</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>ISW_16S</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <OXFORD_NANOPORE>
        <INSTRUMENT_MODEL>MinION</INSTRUMENT_MODEL>
      </OXFORD_NANOPORE>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX11049084" alias="FW_16S">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX11049084</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9777487">FW_16S</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Nanopore sequencing of gut symbionts in Coptotermes heimi</TITLE>
    <STUDY_REF accession="SRP322334">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP322334</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9777487">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Library was prepared using barcoding of PCR amplified products. Basecalling and demultiplexing of Fast5 sequencing reads was done using Guppy program. Next, only high quality reads (q&gt;10) were filtered using using NanoFilt.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS9117118">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS9117118</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|manishagupta293@gmail.com">FW_16S</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>FW_16S</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <OXFORD_NANOPORE>
        <INSTRUMENT_MODEL>MinION</INSTRUMENT_MODEL>
      </OXFORD_NANOPORE>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX11049085" alias="FA_Archaea">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX11049085</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9777487">FA_Archaea</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Nanopore sequencing of gut symbionts in Coptotermes heimi</TITLE>
    <STUDY_REF accession="SRP322334">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP322334</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9777487">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Library was prepared using barcoding of PCR amplified products. Basecalling and demultiplexing of Fast5 sequencing reads was done using Guppy program. Next, only high quality reads (q&gt;10) were filtered using using NanoFilt.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS9117119">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS9117119</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|manishagupta293@gmail.com">FA_Archaea</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>FA_Archaea</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <OXFORD_NANOPORE>
        <INSTRUMENT_MODEL>MinION</INSTRUMENT_MODEL>
      </OXFORD_NANOPORE>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX11049086" alias="MA_Archaea">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX11049086</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9777487">MA_Archaea</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Nanopore sequencing of gut symbionts in Coptotermes heimi</TITLE>
    <STUDY_REF accession="SRP322334">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP322334</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9777487">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Library was prepared using barcoding of PCR amplified products. Basecalling and demultiplexing of Fast5 sequencing reads was done using Guppy program. Next, only high quality reads (q&gt;10) were filtered using using NanoFilt.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS9117120">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS9117120</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|manishagupta293@gmail.com">MA_Archaea</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>MA_Archaea</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <OXFORD_NANOPORE>
        <INSTRUMENT_MODEL>MinION</INSTRUMENT_MODEL>
      </OXFORD_NANOPORE>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX11049087" alias="ISW_Archaea">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX11049087</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9777487">ISW_Archaea</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Nanopore sequencing of gut symbionts in Coptotermes heimi</TITLE>
    <STUDY_REF accession="SRP322334">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP322334</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9777487">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Library was prepared using barcoding of PCR amplified products. Basecalling and demultiplexing of Fast5 sequencing reads was done using Guppy program. Next, only high quality reads (q&gt;10) were filtered using using NanoFilt.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS9117121">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS9117121</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|manishagupta293@gmail.com">ISW_Archaea</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>ISW_Archaea</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <OXFORD_NANOPORE>
        <INSTRUMENT_MODEL>MinION</INSTRUMENT_MODEL>
      </OXFORD_NANOPORE>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX11049088" alias="FW_Archaea">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX11049088</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9777487">FW_Archaea</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Nanopore sequencing of gut symbionts in Coptotermes heimi</TITLE>
    <STUDY_REF accession="SRP322334">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP322334</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9777487">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Library was prepared using barcoding of PCR amplified products. Basecalling and demultiplexing of Fast5 sequencing reads was done using Guppy program. Next, only high quality reads (q&gt;10) were filtered using using NanoFilt.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS9117122">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS9117122</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|manishagupta293@gmail.com">FW_Archaea</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>FW_Archaea</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <OXFORD_NANOPORE>
        <INSTRUMENT_MODEL>MinION</INSTRUMENT_MODEL>
      </OXFORD_NANOPORE>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX11049089" alias="FA_Protist">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX11049089</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9777487">FA_Protist</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Nanopore sequencing of gut symbionts in Coptotermes heimi</TITLE>
    <STUDY_REF accession="SRP322334">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP322334</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9777487">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Library was prepared using barcoding of PCR amplified products. Basecalling and demultiplexing of Fast5 sequencing reads was done using Guppy program. Next, only high quality reads (q&gt;10) were filtered using using NanoFilt.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS9117123">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS9117123</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|manishagupta293@gmail.com">FA_Protist</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>FA_Protist</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <OXFORD_NANOPORE>
        <INSTRUMENT_MODEL>MinION</INSTRUMENT_MODEL>
      </OXFORD_NANOPORE>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX11049090" alias="MA_Protist">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX11049090</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9777487">MA_Protist</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Nanopore sequencing of gut symbionts in Coptotermes heimi</TITLE>
    <STUDY_REF accession="SRP322334">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP322334</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9777487">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Library was prepared using barcoding of PCR amplified products. Basecalling and demultiplexing of Fast5 sequencing reads was done using Guppy program. Next, only high quality reads (q&gt;10) were filtered using using NanoFilt.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS9117124">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS9117124</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|manishagupta293@gmail.com">MA_Protist</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>MA_Protist</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <OXFORD_NANOPORE>
        <INSTRUMENT_MODEL>MinION</INSTRUMENT_MODEL>
      </OXFORD_NANOPORE>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
