<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX5399291" alias="sRNA_Aangustifolia">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5399291</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5210760">sRNA_Aangustifolia</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>sRNAs of Araucaria engustifolia</TITLE>
    <STUDY_REF accession="SRP186414">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP186414</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5210760">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from Brazilian pine fresh leaves. RNA sequencing was performed using the Illumina HiSeq2000 platform, one sRNA library was constructed and sequenced, comprising 28,376,092 single-end reads with a length of 50 bases. The sRNA library building follows a series of standard steps, briefly described as follows: gel purification of the RNA corresponding to fragments ranging from 20-30 nt, ligation of the 3p and 5p adapters separately and followed by gel purification each, cDNA synthesis and cDNA gel purification, and, finally, PCR amplification to generate a cDNA colony template library for deep sequencing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4386195">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4386195</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|margis">sRNAs_Aang001</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>sRNA_Aangustifolia</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
