<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX6849018" alias="AqStamen_pre">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6849018</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6283774">AqStamen_pre</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq  of Stage 11 Aquilegia stamen</TITLE>
    <STUDY_REF accession="SRP221616">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP221616</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB6283774">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was isolated using the Qiagen RNeasy Plant Mini kit (Qiagen, Valencia, CA, USA), including a repeated elution step. RNA quality was analyzed using a NanoDrop 8000 spectrophotometer (Thermofisher) and an Agilent Bioanalyzer. RNA samples with a minimum 2.09 260/280, and RNA integrity number of 7.5 were used as input using the Apollo Prep X PolyA8 mRNA 200 bp beta V1 protocol for single-end library generation. All libraries were quality confirmed for correct size distributions by TapeStation, quantified by QBIT and quantitative PCR using the ABI prism 7900 and Kappa quantification kit and pooled before running on one Illumina HiSeq2500 lane.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5387479">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5387479</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|cmeaders">Stamen Pre</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>AqStamen_pre</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-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 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6849019" alias="AqStaminode_pre">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6849019</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6283774">AqStaminode_pre</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Stage 11 Aquilegia  staminode</TITLE>
    <STUDY_REF accession="SRP221616">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP221616</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB6283774">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was isolated using the Qiagen RNeasy Plant Mini kit (Qiagen, Valencia, CA, USA), including a repeated elution step. RNA quality was analyzed using a NanoDrop 8000 spectrophotometer (Thermofisher) and an Agilent Bioanalyzer. RNA samples with a minimum 2.09 260/280, and RNA integrity number of 7.5 were used as input using the Apollo Prep X PolyA8 mRNA 200 bp beta V1 protocol for single-end library generation. All libraries were quality confirmed for correct size distributions by TapeStation, quantified by QBIT and quantitative PCR using the ABI prism 7900 and Kappa quantification kit and pooled before running on one Illumina HiSeq2500 lane.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5387480">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5387480</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|cmeaders">Staminode Pre</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>AqStaminode_pre</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-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 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6849020" alias="AqStamen_post">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6849020</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6283774">AqStamen_post</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Stage 13 Aquilegia  stamen</TITLE>
    <STUDY_REF accession="SRP221616">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP221616</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB6283774">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was isolated using the Qiagen RNeasy Plant Mini kit (Qiagen, Valencia, CA, USA), including a repeated elution step. RNA quality was analyzed using a NanoDrop 8000 spectrophotometer (Thermofisher) and an Agilent Bioanalyzer. RNA samples with a minimum 2.09 260/280, and RNA integrity number of 7.5 were used as input using the Apollo Prep X PolyA8 mRNA 200 bp beta V1 protocol for single-end library generation. All libraries were quality confirmed for correct size distributions by TapeStation, quantified by QBIT and quantitative PCR using the ABI prism 7900 and Kappa quantification kit and pooled before running on one Illumina HiSeq2500 lane.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5387481">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5387481</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|cmeaders">Stamen Post</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>AqStamen_post</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-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 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6849021" alias="AqStaminode_post">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6849021</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6283774">AqStaminode_post</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Stage 13 Aquilegia  staminode</TITLE>
    <STUDY_REF accession="SRP221616">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP221616</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB6283774">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was isolated using the Qiagen RNeasy Plant Mini kit (Qiagen, Valencia, CA, USA), including a repeated elution step. RNA quality was analyzed using a NanoDrop 8000 spectrophotometer (Thermofisher) and an Agilent Bioanalyzer. RNA samples with a minimum 2.09 260/280, and RNA integrity number of 7.5 were used as input using the Apollo Prep X PolyA8 mRNA 200 bp beta V1 protocol for single-end library generation. All libraries were quality confirmed for correct size distributions by TapeStation, quantified by QBIT and quantitative PCR using the ABI prism 7900 and Kappa quantification kit and pooled before running on one Illumina HiSeq2500 lane.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5387482">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5387482</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|cmeaders">Staminode Post</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>AqStaminode_post</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-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 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
