<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT alias="GSM2857833" accession="SRX3395538">
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      <PRIMARY_ID>SRX3395538</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2857833</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2857833: MOLT16 H3K27ac; Homo sapiens; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP125050" refname="GSE106939">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125050</PRIMARY_ID>
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          <PRIMARY_ID>SRS2689723</PRIMARY_ID>
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          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>2x10^7 cells crosslinked with methanol-free formaldehyde (1% final concentration) RT for 7 min, reaction quenched with glycine . Nuclei isolation performed using truChIP Chromatin Shearing Reagent KIT (Covaris, PN520154). Purified chromatin fragmented by sonication (Covaris, M220, Focused-ultrasonicator). Chromatin fraction ON IP incubation with 40 μl of Protein A UltraLink™ Resin (Thermo-Scientific, 53139) and 4 μg Anti-Histone H3 (acetyl K27) antibody - ChIP Grade (Abcam, ab4729). Day after, bead wash and ON reverse cross-linking by incubation at 65 °C. Input sample was also included (from 1.6x10^6 cells). DNA purified by Chromatin IP DNA Purification Kit (Active-Motif, 58002). library prepared using NEBNext Ultra DNA library Prep Kit (New England Biolabs,E73370S) and sequenced by NextSeq 500 (Illumina). DNA fragmentation, End repair, 5' Phosphorilation, dA-Tailing, Adaptor Ligation with U Excision, Size selection/CleanUp, PCR enrichment, Final CleanUp</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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    <EXPERIMENT_ATTRIBUTES>
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  <EXPERIMENT alias="GSM2857834" accession="SRX3395539">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3395539</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2857834</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2857834: MOLT16 input; Homo sapiens; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP125050" refname="GSE106939">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125050</PRIMARY_ID>
      </IDENTIFIERS>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS2689724</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2857834</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>2x10^7 cells crosslinked with methanol-free formaldehyde (1% final concentration) RT for 7 min, reaction quenched with glycine . Nuclei isolation performed using truChIP Chromatin Shearing Reagent KIT (Covaris, PN520154). Purified chromatin fragmented by sonication (Covaris, M220, Focused-ultrasonicator). Chromatin fraction ON IP incubation with 40 μl of Protein A UltraLink™ Resin (Thermo-Scientific, 53139) and 4 μg Anti-Histone H3 (acetyl K27) antibody - ChIP Grade (Abcam, ab4729). Day after, bead wash and ON reverse cross-linking by incubation at 65 °C. Input sample was also included (from 1.6x10^6 cells). DNA purified by Chromatin IP DNA Purification Kit (Active-Motif, 58002). library prepared using NEBNext Ultra DNA library Prep Kit (New England Biolabs,E73370S) and sequenced by NextSeq 500 (Illumina). DNA fragmentation, End repair, 5' Phosphorilation, dA-Tailing, Adaptor Ligation with U Excision, Size selection/CleanUp, PCR enrichment, Final CleanUp</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
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    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2857834</VALUE>
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    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
</EXPERIMENT_SET>
