<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX17966097" alias="GSM6660161_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17966097</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6660161_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6660161: BM_CR_123; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP403659">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP403659</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA892527</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15482423">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15482423</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6660161</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6660161</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>Ficoll-processed primary BM samples were sorted into CD34+ and CD3+ fractions. Library was performed according to the manufacter's protocol CG000204 (single cell 3' v2 protocol, 10x Genomics). </LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17966098" alias="GSM6660162_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17966098</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6660162_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6660162: BM_REL_123; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP403659">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP403659</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA892527</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15482424">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15482424</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6660162</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6660162</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>Ficoll-processed primary BM samples were sorted into CD34+ and CD3+ fractions. Library was performed according to the manufacter's protocol CG000204 (single cell 3' v2 protocol, 10x Genomics). </LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
