<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX23218825" alias="GSM8016953_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23218825</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM8016953_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM8016953: HMCB cells, siNC, biol rep 1; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP483768">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP483768</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1064891</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS20142014">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20142014</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM8016953</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM8016953</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 harvested using Rneasy mini plus kit (Qiagen) For the non-directional library, it was ready after end repair, A-tailing, adapter ligation, size selection, amplification, and purificationThe library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Quantified libraries will be pooled and sequenced on Illumina platforms, according to effective library concentration and data amount.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23218826" alias="GSM8016954_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23218826</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM8016954_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM8016954: HMCB cells, siNC, biol rep 2; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP483768">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP483768</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1064891</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS20142015">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20142015</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM8016954</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM8016954</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 harvested using Rneasy mini plus kit (Qiagen) For the non-directional library, it was ready after end repair, A-tailing, adapter ligation, size selection, amplification, and purificationThe library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Quantified libraries will be pooled and sequenced on Illumina platforms, according to effective library concentration and data amount.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23218827" alias="GSM8016955_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23218827</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM8016955_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM8016955: HMCB cells, siNC, biol rep 3; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP483768">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP483768</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1064891</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS20142016">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20142016</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM8016955</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM8016955</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 harvested using Rneasy mini plus kit (Qiagen) For the non-directional library, it was ready after end repair, A-tailing, adapter ligation, size selection, amplification, and purificationThe library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Quantified libraries will be pooled and sequenced on Illumina platforms, according to effective library concentration and data amount.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23218828" alias="GSM8016956_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23218828</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM8016956_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM8016956: HMCB cells, siAHCYL1, biol rep 1; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP483768">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP483768</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1064891</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS20142017">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20142017</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM8016956</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM8016956</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 harvested using Rneasy mini plus kit (Qiagen) For the non-directional library, it was ready after end repair, A-tailing, adapter ligation, size selection, amplification, and purificationThe library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Quantified libraries will be pooled and sequenced on Illumina platforms, according to effective library concentration and data amount.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23218829" alias="GSM8016957_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23218829</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM8016957_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM8016957: HMCB cells, siAHCYL1, biol rep 2; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP483768">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP483768</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1064891</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS20142019">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20142019</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM8016957</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM8016957</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 harvested using Rneasy mini plus kit (Qiagen) For the non-directional library, it was ready after end repair, A-tailing, adapter ligation, size selection, amplification, and purificationThe library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Quantified libraries will be pooled and sequenced on Illumina platforms, according to effective library concentration and data amount.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23218830" alias="GSM8016958_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23218830</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM8016958_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM8016958: HMCB cells, siAHCYL1, biol rep 3; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP483768">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP483768</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1064891</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS20142018">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20142018</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM8016958</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM8016958</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 harvested using Rneasy mini plus kit (Qiagen) For the non-directional library, it was ready after end repair, A-tailing, adapter ligation, size selection, amplification, and purificationThe library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Quantified libraries will be pooled and sequenced on Illumina platforms, according to effective library concentration and data amount.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
