<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX23875025" alias="GSM8135555_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23875025</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM8135555_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM8135555: hiPSC-CM, scrambled siRNA, differentiation 1; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP494011">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP494011</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1085328</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS20693544">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20693544</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM8135555</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM8135555</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 issolated using the miRNease Mini Kit (Qiagen). 500 ng of total RNA were used for sequencing librabry construction. Library was prepared utilizing the 'Novogene NGS RNA Library Prep Set (PT042)* (Novogene). Messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand cDNA was synthesized using random hexamer primers followed by the second strand cDNA synthesis. The library was ready after end repair, A-tailing, adapter ligation, size selection, amplification, and purification.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq X Plus</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23875026" alias="GSM8135556_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23875026</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM8135556_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM8135556: hiPSC-CM, scrambled siRNA, differentiation 2; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP494011">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP494011</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1085328</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS20693542">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20693542</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM8135556</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM8135556</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 issolated using the miRNease Mini Kit (Qiagen). 500 ng of total RNA were used for sequencing librabry construction. Library was prepared utilizing the 'Novogene NGS RNA Library Prep Set (PT042)* (Novogene). Messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand cDNA was synthesized using random hexamer primers followed by the second strand cDNA synthesis. The library was ready after end repair, A-tailing, adapter ligation, size selection, amplification, and purification.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq X Plus</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23875027" alias="GSM8135557_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23875027</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM8135557_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM8135557: hiPSC-CM, scrambled siRNA, differentiation 3; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP494011">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP494011</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1085328</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS20693543">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20693543</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM8135557</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM8135557</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 issolated using the miRNease Mini Kit (Qiagen). 500 ng of total RNA were used for sequencing librabry construction. Library was prepared utilizing the 'Novogene NGS RNA Library Prep Set (PT042)* (Novogene). Messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand cDNA was synthesized using random hexamer primers followed by the second strand cDNA synthesis. The library was ready after end repair, A-tailing, adapter ligation, size selection, amplification, and purification.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq X Plus</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23875028" alias="GSM8135558_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23875028</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM8135558_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM8135558: hiPSC-CM, circZFPM2 siRNA, differentiation 1; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP494011">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP494011</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1085328</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS20693546">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20693546</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM8135558</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM8135558</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 issolated using the miRNease Mini Kit (Qiagen). 500 ng of total RNA were used for sequencing librabry construction. Library was prepared utilizing the 'Novogene NGS RNA Library Prep Set (PT042)* (Novogene). Messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand cDNA was synthesized using random hexamer primers followed by the second strand cDNA synthesis. The library was ready after end repair, A-tailing, adapter ligation, size selection, amplification, and purification.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq X Plus</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23875029" alias="GSM8135559_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23875029</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM8135559_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM8135559: hiPSC-CM, circZFPM2 siRNA, differentiation 2; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP494011">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP494011</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1085328</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS20693545">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20693545</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM8135559</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM8135559</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 issolated using the miRNease Mini Kit (Qiagen). 500 ng of total RNA were used for sequencing librabry construction. Library was prepared utilizing the 'Novogene NGS RNA Library Prep Set (PT042)* (Novogene). Messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand cDNA was synthesized using random hexamer primers followed by the second strand cDNA synthesis. The library was ready after end repair, A-tailing, adapter ligation, size selection, amplification, and purification.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq X Plus</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23875030" alias="GSM8135560_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23875030</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM8135560_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM8135560: hiPSC-CM, circZFPM2 siRNA, differentiation 3; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP494011">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP494011</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1085328</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS20693547">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20693547</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM8135560</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM8135560</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 issolated using the miRNease Mini Kit (Qiagen). 500 ng of total RNA were used for sequencing librabry construction. Library was prepared utilizing the 'Novogene NGS RNA Library Prep Set (PT042)* (Novogene). Messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand cDNA was synthesized using random hexamer primers followed by the second strand cDNA synthesis. The library was ready after end repair, A-tailing, adapter ligation, size selection, amplification, and purification.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq X Plus</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
