<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY accession="ERP105123" alias="ena-STUDY-ARO-08-11-2017-07:10:48:763-293" center_name="ARO">
    <IDENTIFIERS>
      <PRIMARY_ID>ERP105123</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject">PRJEB23373</EXTERNAL_ID>
      <SUBMITTER_ID namespace="ARO">ena-STUDY-ARO-08-11-2017-07:10:48:763-293</SUBMITTER_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>Comparative omics and feeding manipulations in chicken indicate a shift of the endocrine role of visceral fat towards reproduction</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Other"/>
      <STUDY_ABSTRACT>Broilers and layer hens, grown up to sexual maturation under free-feeding conditions, differed 4.0-fold in weight and 1.6-fold in ovarian-follicle counts, yet the relative accumulation of visceral fat was comparable. RNA-seq and mass-spectrometry (MS) analyses of visceral fat revealed differentially expressed genes between broilers and layers, 1,106 at the mRNA level (FDR=0.05), and 203 at the protein level (P=0.05). Total RNA was prepared using a RNA isolation kit (miRNeasy, Qiagen). Libraries of cDNA were prepared by the Uppsala sequencing platform from 1 µg RNA using the TruSeq Stranded mRNA Sample Preparation Kit (Illumina Inc, #15031047 Rev E). The libraries were uniquely tagged and sequenced with Illumina HiSeq, producing about 64 million paired-end reads (2 x 124 bp) in two technical replicates, per library</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>Comparative RNA-seq in chicken reveals new reproductive adipokines</CENTER_PROJECT_NAME>
      <STUDY_DESCRIPTION>Broilers and layer hens, grown up to sexual maturation under free-feeding conditions, differed 4.0-fold in weight and 1.6-fold in ovarian-follicle counts, yet the relative accumulation of visceral fat was comparable. RNA-seq and mass-spectrometry (MS) analyses of visceral fat revealed differentially expressed genes between broilers and layers, 1,106 at the mRNA level (FDR=0.05), and 203 at the protein level (P=0.05). Total RNA was prepared using a RNA isolation kit (miRNeasy, Qiagen). Libraries of cDNA were prepared by the Uppsala sequencing platform from 1 µg RNA using the TruSeq Stranded mRNA Sample Preparation Kit (Illumina Inc, #15031047 Rev E). The libraries were uniquely tagged and sequenced with Illumina HiSeq, producing about 64 million paired-end reads (2 x 124 bp) in two technical replicates, per library</STUDY_DESCRIPTION>
    </DESCRIPTOR>
    <STUDY_ATTRIBUTES>
      <STUDY_ATTRIBUTE>
        <TAG>ENA-FIRST-PUBLIC</TAG>
        <VALUE>2018-04-12</VALUE>
      </STUDY_ATTRIBUTE>
      <STUDY_ATTRIBUTE>
        <TAG>ENA-LAST-UPDATE</TAG>
        <VALUE>2017-11-08</VALUE>
      </STUDY_ATTRIBUTE>
    </STUDY_ATTRIBUTES>
  </STUDY>
</STUDY_SET>
