<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY center_name="BioCI" alias="a74d638a-9a3f-11e7-9f06-000e1e0af2dc" accession="SRP118719">
    <IDENTIFIERS>
      <PRIMARY_ID>SRP118719</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject" label="primary">PRJNA411848</EXTERNAL_ID>
      <SUBMITTER_ID namespace="BioCI">a74d638a-9a3f-11e7-9f06-000e1e0af2dc</SUBMITTER_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>Zea mays B73, seedling root tip (0-5mm), whole chromatin, H3K27me3 ChIP</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Whole Genome Sequencing"/>
      <STUDY_ABSTRACT>The terminal 0-5 mm root segments of B73 seedling roots were excised, fixed in 1% formaldehyde for 15 minutes, washed in PBS, and snap frozen. Chromatin was extracted from frozen roots and used for ChIP with an anti-H3K27me3 antibody (Millipore, 07-449, lot 2275589) and the resulting DNA Illumina sequenced.</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>a74d638a-9a3f-11e7-9f06-000e1e0af2dc</CENTER_PROJECT_NAME>
    </DESCRIPTOR>
  </STUDY>
</STUDY_SET>
