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      <PRIMARY_ID>SRX22382794</PRIMARY_ID>
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    </IDENTIFIERS>
    <TITLE>GSM7883264: N2,OP50,no antibiotic,1; Caenorhabditis elegans; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP470375">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP470375</PRIMARY_ID>
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      <SAMPLE_DESCRIPTOR accession="SRS19429026">
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          <PRIMARY_ID>SRS19429026</PRIMARY_ID>
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        <LIBRARY_NAME>GSM7883264</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted using with Trizol (Invitrogen). Genomic DNA contamination was removed using Turbo DNase (Qiagen). Messenger RNA was purified from total RNA using poly-T oligo attached magnetic beads, followed by cDNA synthesis from mRNA fragments using random hexamer primers prepared by Novogene</LIBRARY_CONSTRUCTION_PROTOCOL>
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        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX22382795</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7883265_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7883265: N2,OP50,no antibiotic,2; Caenorhabditis elegans; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP470375">
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        <PRIMARY_ID>SRP470375</PRIMARY_ID>
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          <PRIMARY_ID>SRS19429028</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7883265</EXTERNAL_ID>
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        <LIBRARY_NAME>GSM7883265</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted using with Trizol (Invitrogen). Genomic DNA contamination was removed using Turbo DNase (Qiagen). Messenger RNA was purified from total RNA using poly-T oligo attached magnetic beads, followed by cDNA synthesis from mRNA fragments using random hexamer primers prepared by Novogene</LIBRARY_CONSTRUCTION_PROTOCOL>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
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  <EXPERIMENT accession="SRX22382796" alias="GSM7883266_r1">
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      <PRIMARY_ID>SRX22382796</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7883266_r1</EXTERNAL_ID>
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    <TITLE>GSM7883266: N2,OP50,no antibiotic,3; Caenorhabditis elegans; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP470375">
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        <PRIMARY_ID>SRP470375</PRIMARY_ID>
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      <SAMPLE_DESCRIPTOR accession="SRS19429027">
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          <PRIMARY_ID>SRS19429027</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7883266</EXTERNAL_ID>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7883266</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted using with Trizol (Invitrogen). Genomic DNA contamination was removed using Turbo DNase (Qiagen). Messenger RNA was purified from total RNA using poly-T oligo attached magnetic beads, followed by cDNA synthesis from mRNA fragments using random hexamer primers prepared by Novogene</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
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  <EXPERIMENT accession="SRX22382797" alias="GSM7883267_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22382797</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7883267_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7883267: N2,OP50,neomycin,1; Caenorhabditis elegans; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP470375">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP470375</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS19429029">
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          <PRIMARY_ID>SRS19429029</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7883267</EXTERNAL_ID>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7883267</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted using with Trizol (Invitrogen). Genomic DNA contamination was removed using Turbo DNase (Qiagen). Messenger RNA was purified from total RNA using poly-T oligo attached magnetic beads, followed by cDNA synthesis from mRNA fragments using random hexamer primers prepared by Novogene</LIBRARY_CONSTRUCTION_PROTOCOL>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
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  <EXPERIMENT accession="SRX22382798" alias="GSM7883268_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22382798</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7883268_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7883268: N2,OP50,neomycin,2; Caenorhabditis elegans; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP470375">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP470375</PRIMARY_ID>
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      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS19429030">
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          <PRIMARY_ID>SRS19429030</PRIMARY_ID>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7883268</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted using with Trizol (Invitrogen). Genomic DNA contamination was removed using Turbo DNase (Qiagen). Messenger RNA was purified from total RNA using poly-T oligo attached magnetic beads, followed by cDNA synthesis from mRNA fragments using random hexamer primers prepared by Novogene</LIBRARY_CONSTRUCTION_PROTOCOL>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
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  <EXPERIMENT accession="SRX22382799" alias="GSM7883269_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22382799</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7883269_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7883269: N2,OP50,neomycin,3; Caenorhabditis elegans; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP470375">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP470375</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1036219</EXTERNAL_ID>
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      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS19429031">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19429031</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7883269</EXTERNAL_ID>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7883269</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted using with Trizol (Invitrogen). Genomic DNA contamination was removed using Turbo DNase (Qiagen). Messenger RNA was purified from total RNA using poly-T oligo attached magnetic beads, followed by cDNA synthesis from mRNA fragments using random hexamer primers prepared by Novogene</LIBRARY_CONSTRUCTION_PROTOCOL>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
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  <EXPERIMENT accession="SRX22382800" alias="GSM7883270_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22382800</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7883270_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7883270: N2_CeMbio, no antibiotic,1; Caenorhabditis elegans; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP470375">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP470375</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS19429032">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19429032</PRIMARY_ID>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7883270</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted using with Trizol (Invitrogen). Genomic DNA contamination was removed using Turbo DNase (Qiagen). Messenger RNA was purified from total RNA using poly-T oligo attached magnetic beads, followed by cDNA synthesis from mRNA fragments using random hexamer primers prepared by Novogene</LIBRARY_CONSTRUCTION_PROTOCOL>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
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  <EXPERIMENT accession="SRX22382801" alias="GSM7883271_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22382801</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7883271_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7883271: N2_CeMbio, no antibiotic,2; Caenorhabditis elegans; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP470375">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP470375</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS19429033">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19429033</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7883271</EXTERNAL_ID>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7883271</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted using with Trizol (Invitrogen). Genomic DNA contamination was removed using Turbo DNase (Qiagen). Messenger RNA was purified from total RNA using poly-T oligo attached magnetic beads, followed by cDNA synthesis from mRNA fragments using random hexamer primers prepared by Novogene</LIBRARY_CONSTRUCTION_PROTOCOL>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
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  <EXPERIMENT accession="SRX22382802" alias="GSM7883272_r1">
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      <PRIMARY_ID>SRX22382802</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7883272_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7883272: N2_CeMbio, no antibiotic,3; Caenorhabditis elegans; RNA-Seq</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP470375</PRIMARY_ID>
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      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS19429034">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19429034</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7883272</EXTERNAL_ID>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7883272</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted using with Trizol (Invitrogen). Genomic DNA contamination was removed using Turbo DNase (Qiagen). Messenger RNA was purified from total RNA using poly-T oligo attached magnetic beads, followed by cDNA synthesis from mRNA fragments using random hexamer primers prepared by Novogene</LIBRARY_CONSTRUCTION_PROTOCOL>
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        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX22382803</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7883273_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7883273: N2, CeMbio, neomycin, 1; Caenorhabditis elegans; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP470375">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP470375</PRIMARY_ID>
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      <SAMPLE_DESCRIPTOR accession="SRS19429035">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19429035</PRIMARY_ID>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7883273</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted using with Trizol (Invitrogen). Genomic DNA contamination was removed using Turbo DNase (Qiagen). Messenger RNA was purified from total RNA using poly-T oligo attached magnetic beads, followed by cDNA synthesis from mRNA fragments using random hexamer primers prepared by Novogene</LIBRARY_CONSTRUCTION_PROTOCOL>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <PRIMARY_ID>SRX22382804</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7883274_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7883274: N2, CeMbio, neomycin, 2; Caenorhabditis elegans; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP470375">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP470375</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1036219</EXTERNAL_ID>
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      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS19429036">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19429036</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7883274</EXTERNAL_ID>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7883274</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted using with Trizol (Invitrogen). Genomic DNA contamination was removed using Turbo DNase (Qiagen). Messenger RNA was purified from total RNA using poly-T oligo attached magnetic beads, followed by cDNA synthesis from mRNA fragments using random hexamer primers prepared by Novogene</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX22382805</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7883275_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7883275: N2, CeMbio, neomycin, 3; Caenorhabditis elegans; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP470375">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP470375</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1036219</EXTERNAL_ID>
      </IDENTIFIERS>
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    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS19429037">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19429037</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7883275</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7883275</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted using with Trizol (Invitrogen). Genomic DNA contamination was removed using Turbo DNase (Qiagen). Messenger RNA was purified from total RNA using poly-T oligo attached magnetic beads, followed by cDNA synthesis from mRNA fragments using random hexamer primers prepared by Novogene</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
