<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY accession="ERP104866" alias="ena-STUDY-UIT-20-10-2017-17:21:49:492-16" center_name="University of Tromso, NORWAY">
    <IDENTIFIERS>
      <PRIMARY_ID>ERP104866</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject">PRJEB23133</EXTERNAL_ID>
      <SUBMITTER_ID namespace="UIT">ena-STUDY-UIT-20-10-2017-17:21:49:492-16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="University of Tromso, NORWAY">ena-STUDY-UIT-20-10-2017-17:21:49:492-16</SUBMITTER_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>Draft genome assembly of Anemonia viridis, mainly aimed for novel miRNA identification</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Other"/>
      <STUDY_ABSTRACT>DNA from one individual of Anemonia viridis (sampled at pH 8.2 outside Sicily, Italy) was sequenced using Illumina HiSeq 2500 platform, yielding 144 million paired-end reads. These reads were assembled using Planatus assembly software. This draft genome assembly was not specifically filtered for symbiont reads.</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>Draft genome assembly of Anemonia viridis</CENTER_PROJECT_NAME>
      <STUDY_DESCRIPTION>DNA from one individual of Anemonia viridis (sampled at pH 8.2 outside Sicily, Italy) was sequenced using Illumina HiSeq 2500 platform, yielding 144 million paired-end reads. These reads were assembled using Planatus assembly software. This draft genome assembly was not specifically filtered for symbiont reads.</STUDY_DESCRIPTION>
    </DESCRIPTOR>
    <STUDY_ATTRIBUTES>
      <STUDY_ATTRIBUTE>
        <TAG>ENA-FIRST-PUBLIC</TAG>
        <VALUE>2018-07-23</VALUE>
      </STUDY_ATTRIBUTE>
      <STUDY_ATTRIBUTE>
        <TAG>ENA-LAST-UPDATE</TAG>
        <VALUE>2017-10-20</VALUE>
      </STUDY_ATTRIBUTE>
    </STUDY_ATTRIBUTES>
  </STUDY>
</STUDY_SET>
