<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX22495669" alias="GSM7892677_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22495669</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7892677_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7892677: Melanoma co-cultured LEC; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP471403">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP471403</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1039499</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS19508641">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19508641</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7892677</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7892677</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>Endothelial cells were sorted with flow cytometry using BD Influx. 4% BSA in PBS was added to the cell suspension to a final concentration of 0.04% and the cell viability and concentration was measured.  Cells were kept on ice until continuation of the 10X Genomics Single Cell Protocol. The Chromium Single Cell 3'RNAseq run and library preparation were done using the Chromium™ Single Cell 3' Reagent version 2 chemistry</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22495670" alias="GSM7892678_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22495670</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7892678_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7892678: Parental monotypic LEC+WM852; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP471403">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP471403</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1039499</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS19508640">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19508640</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7892678</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7892678</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>Endothelial cells were sorted with flow cytometry using BD Influx. 4% BSA in PBS was added to the cell suspension to a final concentration of 0.04% and the cell viability and concentration was measured.  Cells were kept on ice until continuation of the 10X Genomics Single Cell Protocol. The Chromium Single Cell 3'RNAseq run and library preparation were done using the Chromium™ Single Cell 3' Reagent version 2 chemistry</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
