<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX18321254" alias="GSM6743940_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18321254</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6743940_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6743940: Blastoid_4CL, scRNAseq; Macaca fascicularis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408762">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408762</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA903392</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15811543">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15811543</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6743940</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6743940</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC SINGLE CELL</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Monkey blastoids were picked up manually by mouth pipette. Then blastoids were washed with PBS containing 0.05% BSA and dissociated with trypsin-EDTA (0.25%) (Gibco) at 37 °C in 5% CO2 for 10 min. The dissociation was terminated by PBS with 15% FBS and centrifuged the sample at 300g for 5 min. Cell pellets were resuspended in PBS containing 0.05% BSA, filtered through a 40-μm cell strainer and counted. Single-cell suspensions were loaded into a 10X Genomics Chromium Chip following the manufacturer's instructions 48 (10X Genomics, Chromium Next GEM Single Cell 3ʹ GEM, Library and Gel Bead Kit v.3.1).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18321255" alias="GSM6743941_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18321255</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6743941_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6743941: Blastoid_4CL_IVC, scRNAseq; Macaca fascicularis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408762">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408762</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA903392</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15811544">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15811544</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6743941</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6743941</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC SINGLE CELL</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Monkey blastoids were picked up manually by mouth pipette. Then blastoids were washed with PBS containing 0.05% BSA and dissociated with trypsin-EDTA (0.25%) (Gibco) at 37 °C in 5% CO2 for 10 min. The dissociation was terminated by PBS with 15% FBS and centrifuged the sample at 300g for 5 min. Cell pellets were resuspended in PBS containing 0.05% BSA, filtered through a 40-μm cell strainer and counted. Single-cell suspensions were loaded into a 10X Genomics Chromium Chip following the manufacturer's instructions 48 (10X Genomics, Chromium Next GEM Single Cell 3ʹ GEM, Library and Gel Bead Kit v.3.1).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
