<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX17954066" alias="GSM6658181_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17954066</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6658181_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6658181: 4T1MDSC T1; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP403453">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP403453</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA892044</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15471211">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15471211</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6658181</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6658181</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>treated or untreated 4T1 cells were lysing in the well directly. RNA was isolated using RNeasy plus mini (Qiagen) following manufacturer's instructions. Isolated RNA sample quality was assessed by HS Total RNA 15nt on Fragment Analyzer (Agilent Technologies Inc., California, USA) and quantified by Qubit 2.0 RNA HS assay (ThermoFisher, Massachusetts, USA). Truseq Stranded RNA</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17954067" alias="GSM6658182_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17954067</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6658182_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6658182: 4T1MDSC T2; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP403453">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP403453</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA892044</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15471212">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15471212</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6658182</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6658182</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>treated or untreated 4T1 cells were lysing in the well directly. RNA was isolated using RNeasy plus mini (Qiagen) following manufacturer's instructions. Isolated RNA sample quality was assessed by HS Total RNA 15nt on Fragment Analyzer (Agilent Technologies Inc., California, USA) and quantified by Qubit 2.0 RNA HS assay (ThermoFisher, Massachusetts, USA). Truseq Stranded RNA</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17954068" alias="GSM6658183_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17954068</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6658183_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6658183: 4T1MDSC T3; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP403453">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP403453</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA892044</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15471213">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15471213</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6658183</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6658183</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>treated or untreated 4T1 cells were lysing in the well directly. RNA was isolated using RNeasy plus mini (Qiagen) following manufacturer's instructions. Isolated RNA sample quality was assessed by HS Total RNA 15nt on Fragment Analyzer (Agilent Technologies Inc., California, USA) and quantified by Qubit 2.0 RNA HS assay (ThermoFisher, Massachusetts, USA). Truseq Stranded RNA</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17954069" alias="GSM6658184_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17954069</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6658184_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6658184: 4T1MDSC T4; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP403453">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP403453</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA892044</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15471214">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15471214</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6658184</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6658184</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>treated or untreated 4T1 cells were lysing in the well directly. RNA was isolated using RNeasy plus mini (Qiagen) following manufacturer's instructions. Isolated RNA sample quality was assessed by HS Total RNA 15nt on Fragment Analyzer (Agilent Technologies Inc., California, USA) and quantified by Qubit 2.0 RNA HS assay (ThermoFisher, Massachusetts, USA). Truseq Stranded RNA</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17954070" alias="GSM6658185_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17954070</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6658185_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6658185: 4T1MDSC S1; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP403453">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP403453</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA892044</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15471215">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15471215</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6658185</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6658185</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>treated or untreated 4T1 cells were lysing in the well directly. RNA was isolated using RNeasy plus mini (Qiagen) following manufacturer's instructions. Isolated RNA sample quality was assessed by HS Total RNA 15nt on Fragment Analyzer (Agilent Technologies Inc., California, USA) and quantified by Qubit 2.0 RNA HS assay (ThermoFisher, Massachusetts, USA). Truseq Stranded RNA</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17954071" alias="GSM6658186_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17954071</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6658186_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6658186: 4T1MDSC S2; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP403453">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP403453</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA892044</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15471216">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15471216</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6658186</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6658186</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>treated or untreated 4T1 cells were lysing in the well directly. RNA was isolated using RNeasy plus mini (Qiagen) following manufacturer's instructions. Isolated RNA sample quality was assessed by HS Total RNA 15nt on Fragment Analyzer (Agilent Technologies Inc., California, USA) and quantified by Qubit 2.0 RNA HS assay (ThermoFisher, Massachusetts, USA). Truseq Stranded RNA</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17954072" alias="GSM6658187_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17954072</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6658187_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6658187: 4T1MDSC S3; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP403453">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP403453</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA892044</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15471217">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15471217</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6658187</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6658187</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>treated or untreated 4T1 cells were lysing in the well directly. RNA was isolated using RNeasy plus mini (Qiagen) following manufacturer's instructions. Isolated RNA sample quality was assessed by HS Total RNA 15nt on Fragment Analyzer (Agilent Technologies Inc., California, USA) and quantified by Qubit 2.0 RNA HS assay (ThermoFisher, Massachusetts, USA). Truseq Stranded RNA</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17954073" alias="GSM6658188_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17954073</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6658188_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6658188: 4T1MDSC S4; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP403453">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP403453</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA892044</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15471218">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15471218</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6658188</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6658188</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>treated or untreated 4T1 cells were lysing in the well directly. RNA was isolated using RNeasy plus mini (Qiagen) following manufacturer's instructions. Isolated RNA sample quality was assessed by HS Total RNA 15nt on Fragment Analyzer (Agilent Technologies Inc., California, USA) and quantified by Qubit 2.0 RNA HS assay (ThermoFisher, Massachusetts, USA). Truseq Stranded RNA</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17954074" alias="GSM6658189_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17954074</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6658189_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6658189: 4T1_1; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP403453">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP403453</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA892044</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15471219">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15471219</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6658189</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6658189</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>treated or untreated 4T1 cells were lysing in the well directly. RNA was isolated using RNeasy plus mini (Qiagen) following manufacturer's instructions. Isolated RNA sample quality was assessed by HS Total RNA 15nt on Fragment Analyzer (Agilent Technologies Inc., California, USA) and quantified by Qubit 2.0 RNA HS assay (ThermoFisher, Massachusetts, USA). Truseq Stranded RNA</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17954075" alias="GSM6658190_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17954075</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6658190_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6658190: 4T1_2; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP403453">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP403453</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA892044</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15471220">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15471220</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6658190</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6658190</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>treated or untreated 4T1 cells were lysing in the well directly. RNA was isolated using RNeasy plus mini (Qiagen) following manufacturer's instructions. Isolated RNA sample quality was assessed by HS Total RNA 15nt on Fragment Analyzer (Agilent Technologies Inc., California, USA) and quantified by Qubit 2.0 RNA HS assay (ThermoFisher, Massachusetts, USA). Truseq Stranded RNA</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17954076" alias="GSM6658191_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17954076</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6658191_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6658191: 4T1_3; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP403453">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP403453</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA892044</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15471221">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15471221</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6658191</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6658191</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>treated or untreated 4T1 cells were lysing in the well directly. RNA was isolated using RNeasy plus mini (Qiagen) following manufacturer's instructions. Isolated RNA sample quality was assessed by HS Total RNA 15nt on Fragment Analyzer (Agilent Technologies Inc., California, USA) and quantified by Qubit 2.0 RNA HS assay (ThermoFisher, Massachusetts, USA). Truseq Stranded RNA</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17954077" alias="GSM6658192_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17954077</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6658192_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6658192: 4T1_4; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP403453">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP403453</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA892044</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15471222">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15471222</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6658192</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6658192</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>treated or untreated 4T1 cells were lysing in the well directly. RNA was isolated using RNeasy plus mini (Qiagen) following manufacturer's instructions. Isolated RNA sample quality was assessed by HS Total RNA 15nt on Fragment Analyzer (Agilent Technologies Inc., California, USA) and quantified by Qubit 2.0 RNA HS assay (ThermoFisher, Massachusetts, USA). Truseq Stranded RNA</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
