<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY center_name="University of Münster" alias="GS 20/FLX  Pisum sativum" accession="SRP006313">
    <IDENTIFIERS>
      <PRIMARY_ID>SRP006313</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject" label="primary">PRJNA80025</EXTERNAL_ID>
      <SUBMITTER_ID namespace="University of Münster">GS 20/FLX  Pisum sativum</SUBMITTER_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>Pisum sativum Transcriptome or Gene expression</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Other"/>
      <STUDY_ABSTRACT>RNA was extracted from various leaf tissues of multiple individuals of the garden pea, Pisum sativum, including cotyledons (COT), epicotyl (EPI), flowers (FLO), hypocotyl (HYP), leaf (LVN.1, LVN.2, LVN.3, LVN.4, LVN.5, LVR.1) and from seedling grown under normal light (L) or etiolated (E) conditions. RNA was reverse transcribed enriching for full length transcripts and all libraries except leaf library LVR.1 were normalized by cDNA normalization. Libraries LVN.1, LVN.2, LVN.3, LVN.4, FLO and HYP were each sequenced one 454 plate with the GS 20 and libraries COT, EPI, LVN.5, E and L with the GS FLX Standard, libs E and L on half a plate each.</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>Pisum sativum</CENTER_PROJECT_NAME>
    </DESCRIPTOR>
    <STUDY_LINKS>
      <STUDY_LINK>
        <XREF_LINK>
          <DB>pubmed</DB>
          <ID>21569327</ID>
        </XREF_LINK>
      </STUDY_LINK>
    </STUDY_LINKS>
  </STUDY>
</STUDY_SET>
