<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX20233053" alias="GSM7300316_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX20233053</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7300316_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7300316: MEIS ChIP-seq of E14.5 GE; Mus musculus; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP436120">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP436120</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA967672</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS17567406">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17567406</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7300316</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7300316</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>For ChIP-seq, ganglionic eminences and part of the underlying striatum of 70 embryos at E14.5 were microdissected and immediately fixed in 1% formaldehyde for 5 min. Samples were processed using the ChIP-IT High Sensitivity columns (Active Motif) ChIP-seq libraries were prepared using the NEBNext Ultra II DNA Library Prep Kit for Illumina (New England Biolabs). 3 ng of DNA was used as starting material for input and ip samples. Libraries were amplified using 12 cycles on the thermocycler. Libraries were validated using the Agilent High Sensitivity DNA Kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX20233054" alias="GSM7300317_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX20233054</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7300317_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7300317: Input of E14.5 GE; Mus musculus; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP436120">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP436120</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA967672</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS17567407">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17567407</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7300317</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7300317</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>For ChIP-seq, ganglionic eminences and part of the underlying striatum of 70 embryos at E14.5 were microdissected and immediately fixed in 1% formaldehyde for 5 min. Samples were processed using the ChIP-IT High Sensitivity columns (Active Motif) ChIP-seq libraries were prepared using the NEBNext Ultra II DNA Library Prep Kit for Illumina (New England Biolabs). 3 ng of DNA was used as starting material for input and ip samples. Libraries were amplified using 12 cycles on the thermocycler. Libraries were validated using the Agilent High Sensitivity DNA Kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
