<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX980531" center_name="Agency for Science Technology and Research" alias="D.gigas Beak Transcriptome">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX980531</PRIMARY_ID>
      <SUBMITTER_ID namespace="Agency for Science Technology and Research">D.gigas Beak Transcriptome</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Squid beak mechanical gradient is defined by infiltration of chitin by protein coacervates</TITLE>
    <STUDY_REF accession="SRP017243">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP017243</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA181271</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA-Seq analysis was performed as previously described17,47. Briefly, total RNA from a D. gigas buccal mass (tissue that was in close proximity to the upper and lower beak were combined and used) was extracted with a Qiagen RNeasy mini kit. Poly-A mRNA was then enriched from 10 µg of total RNA with oligo dT beads (Invitrogen). The buccal mass sample was collected on R/V New Horizon (Scripps Institute of Oceanography, San Diego, CA, USA), June 2010, at Guayamas Basin, Mexico, with Permit No. DAPA/2/100510/1640.  ~100 ng of recovered poly-A mRNA was used to construct an RNA-seq library (ScriptSeqTM mRNA-Seq library kit v1, Epicenter, Illumina) according to manufacturer’s instructions. Phusion PCR polymerase (Thermo Scientific) was used for the final library amplification (12 cycles). PCR cleanup was performed with the MinElute PCR purification kit (Qiagen) and the library quality was assessed with an Agilent 21000 Bioanalyzer. The library was then sequenced on an Illumina GA IIx and 2 lanes of 2x76 bp paired-end-reads were collected.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS895470">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS895470</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="76" NOMINAL_SDEV="0.0E0"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>152</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>77</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina Genome Analyzer IIx</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <PROCESSING>
      <PIPELINE>
        <PIPE_SECTION>
          <STEP_INDEX/>
          <PREV_STEP_INDEX/>
          <PROGRAM>Trinity</PROGRAM>
          <VERSION>r2013-06-08</VERSION>
        </PIPE_SECTION>
      </PIPELINE>
    </PROCESSING>
  </EXPERIMENT>
</EXPERIMENT_SET>
