<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY center_name="GEO" alias="GSE179060" accession="SRP325881">
    <IDENTIFIERS>
      <PRIMARY_ID>SRP325881</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject" label="primary">PRJNA742041</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSE179060</EXTERNAL_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>Chiffon triggers global histone H3 acetylation and expression of developmental genes in Drosophila embryos [ada2b]</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Transcriptome Analysis"/>
      <STUDY_ABSTRACT>Purpose: The goal of this study was to identify the differential expressed genes in the Drosophila embryo when ada2b is disrupted. Overall design: Method: RNA extracted from Drosophila embryos (stage 12-14) was used to generate cDNA libraries using NuGen Ovation RNA-seq System V2. Samples were sequenced using Ilumina HiSeq150 next generation sequencer (four biological replicates per genotype: ada2b null mutants flies, and the rescue of different transgenes: Ada2b_PA, Ada2b_PB, A34908116da2b_PA+Ada2b_PB, and a WT control.</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>GSE179060</CENTER_PROJECT_NAME>
    </DESCRIPTOR>
    <STUDY_LINKS>
      <STUDY_LINK>
        <XREF_LINK>
          <DB>pubmed</DB>
          <ID>34908116</ID>
        </XREF_LINK>
      </STUDY_LINK>
    </STUDY_LINKS>
    <STUDY_ATTRIBUTES>
      <STUDY_ATTRIBUTE>
        <TAG>parent_bioproject</TAG>
        <VALUE>PRJNA742034</VALUE>
      </STUDY_ATTRIBUTE>
    </STUDY_ATTRIBUTES>
  </STUDY>
</STUDY_SET>
