<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX23528714" alias="WW01">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23528714</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14199933">WW01</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>WW01</TITLE>
    <STUDY_REF accession="SRP487742">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP487742</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1072624</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Samples were pooled in equimolar ratio. The pool was checked on using a DNA-HS tape on the Tapestation and found to contain adapter dimer so an additional bead clean using AmpureXP in a 1:1 ratio was undertaken to remove this dimer. The pool was checked again using DNA-HS and the dimer was confirmed to be removed (see NVS030_Pool_QC for comparison of before and after)</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20378259">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20378259</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|desi_utami@orcid">Warlock_4</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>WW01</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23528715" alias="WW11">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23528715</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14199933">WW11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>WW11</TITLE>
    <STUDY_REF accession="SRP487742">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP487742</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1072624</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Samples were pooled in equimolar ratio. The pool was checked on using a DNA-HS tape on the Tapestation and found to contain adapter dimer so an additional bead clean using AmpureXP in a 1:1 ratio was undertaken to remove this dimer. The pool was checked again using DNA-HS and the dimer was confirmed to be removed (see NVS030_Pool_QC for comparison of before and after)</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20378260">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20378260</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|desi_utami@orcid">Warlock_5</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>WW11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23528716" alias="WW21">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23528716</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14199933">WW21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>WW21</TITLE>
    <STUDY_REF accession="SRP487742">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP487742</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1072624</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Samples were pooled in equimolar ratio. The pool was checked on using a DNA-HS tape on the Tapestation and found to contain adapter dimer so an additional bead clean using AmpureXP in a 1:1 ratio was undertaken to remove this dimer. The pool was checked again using DNA-HS and the dimer was confirmed to be removed (see NVS030_Pool_QC for comparison of before and after)</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20378261">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20378261</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|desi_utami@orcid">Warlock_6</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>WW21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23528717" alias="WW02">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23528717</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14199933">WW02</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>WW02</TITLE>
    <STUDY_REF accession="SRP487742">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP487742</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1072624</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Samples were pooled in equimolar ratio. The pool was checked on using a DNA-HS tape on the Tapestation and found to contain adapter dimer so an additional bead clean using AmpureXP in a 1:1 ratio was undertaken to remove this dimer. The pool was checked again using DNA-HS and the dimer was confirmed to be removed (see NVS030_Pool_QC for comparison of before and after)</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20378262">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20378262</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|desi_utami@orcid">Warlock_10</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>WW02</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23528718" alias="WW12">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23528718</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14199933">WW12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>WW12</TITLE>
    <STUDY_REF accession="SRP487742">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP487742</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1072624</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Samples were pooled in equimolar ratio. The pool was checked on using a DNA-HS tape on the Tapestation and found to contain adapter dimer so an additional bead clean using AmpureXP in a 1:1 ratio was undertaken to remove this dimer. The pool was checked again using DNA-HS and the dimer was confirmed to be removed (see NVS030_Pool_QC for comparison of before and after)</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20378263">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20378263</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|desi_utami@orcid">Warlock_11</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>WW12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23528719" alias="WW22">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23528719</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14199933">WW22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>WW22</TITLE>
    <STUDY_REF accession="SRP487742">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP487742</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1072624</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Samples were pooled in equimolar ratio. The pool was checked on using a DNA-HS tape on the Tapestation and found to contain adapter dimer so an additional bead clean using AmpureXP in a 1:1 ratio was undertaken to remove this dimer. The pool was checked again using DNA-HS and the dimer was confirmed to be removed (see NVS030_Pool_QC for comparison of before and after)</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20378264">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20378264</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|desi_utami@orcid">Warlock_12</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>WW22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23528720" alias="WW03">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23528720</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14199933">WW03</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>WW03</TITLE>
    <STUDY_REF accession="SRP487742">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP487742</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1072624</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Samples were pooled in equimolar ratio. The pool was checked on using a DNA-HS tape on the Tapestation and found to contain adapter dimer so an additional bead clean using AmpureXP in a 1:1 ratio was undertaken to remove this dimer. The pool was checked again using DNA-HS and the dimer was confirmed to be removed (see NVS030_Pool_QC for comparison of before and after)</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20378265">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20378265</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|desi_utami@orcid">Warlock_16</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>WW03</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23528721" alias="WW13">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23528721</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14199933">WW13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>WW13</TITLE>
    <STUDY_REF accession="SRP487742">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP487742</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1072624</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Samples were pooled in equimolar ratio. The pool was checked on using a DNA-HS tape on the Tapestation and found to contain adapter dimer so an additional bead clean using AmpureXP in a 1:1 ratio was undertaken to remove this dimer. The pool was checked again using DNA-HS and the dimer was confirmed to be removed (see NVS030_Pool_QC for comparison of before and after)</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20378266">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20378266</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|desi_utami@orcid">Warlock_17</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>WW13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23528722" alias="WW23">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23528722</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14199933">WW23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>WW23</TITLE>
    <STUDY_REF accession="SRP487742">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP487742</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1072624</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Samples were pooled in equimolar ratio. The pool was checked on using a DNA-HS tape on the Tapestation and found to contain adapter dimer so an additional bead clean using AmpureXP in a 1:1 ratio was undertaken to remove this dimer. The pool was checked again using DNA-HS and the dimer was confirmed to be removed (see NVS030_Pool_QC for comparison of before and after)</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20378267">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20378267</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|desi_utami@orcid">Warlock_18</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>WW23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
