<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX12192127" alias="R1_9">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192127</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">R1_9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Chondrolia Chalkidikis: young_leaf_rep1</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Chondrolia Chalkidikis" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The biological replicates per tissue type were equimolarly mixed in 2 g final RNA pools. The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the EBNext Multiplex Oligos for Illumina (Set 1 and 2) kit (, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the QubitTM dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 5200 Fragment Analyzer (Agilent Technology Inc., CA, USA) according to DNF-473-33 - SS NGS Fragment 1-6000bp protocol, and the KAPA library Quantification kit (KAPA Biosystems, Cape Town, South Africa).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169826">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169826</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">CH_young_leaf</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>R1_9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192128" alias="R2_9">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192128</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">R2_9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Chondrolia Chalkidikis: young_leaf_rep2</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Chondrolia Chalkidikis" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The biological replicates per tissue type were equimolarly mixed in 2 g final RNA pools. The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the EBNext Multiplex Oligos for Illumina (Set 1 and 2) kit (, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the QubitTM dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 5200 Fragment Analyzer (Agilent Technology Inc., CA, USA) according to DNF-473-33 - SS NGS Fragment 1-6000bp protocol, and the KAPA library Quantification kit (KAPA Biosystems, Cape Town, South Africa).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169826">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169826</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">CH_young_leaf</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>R2_9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192129" alias="R2_13">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192129</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">R2_13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Chondrolia Chalkidikis: mature_shoot_rep2</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Chondrolia Chalkidikis" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The biological replicates per tissue type were equimolarly mixed in 2 g final RNA pools. The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the EBNext Multiplex Oligos for Illumina (Set 1 and 2) kit (, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the QubitTM dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 5200 Fragment Analyzer (Agilent Technology Inc., CA, USA) according to DNF-473-33 - SS NGS Fragment 1-6000bp protocol, and the KAPA library Quantification kit (KAPA Biosystems, Cape Town, South Africa).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169827">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169827</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">CH_mature_shoot</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>R2_13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192130" alias="R3_13">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192130</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">R3_13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Chondrolia Chalkidikis: mature_shoot_rep3</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Chondrolia Chalkidikis" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The biological replicates per tissue type were equimolarly mixed in 2 g final RNA pools. The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the EBNext Multiplex Oligos for Illumina (Set 1 and 2) kit (, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the QubitTM dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 5200 Fragment Analyzer (Agilent Technology Inc., CA, USA) according to DNF-473-33 - SS NGS Fragment 1-6000bp protocol, and the KAPA library Quantification kit (KAPA Biosystems, Cape Town, South Africa).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169827">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169827</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">CH_mature_shoot</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>R3_13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192131" alias="R1_2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192131</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">R1_2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Chondrolia Chalkidikis: closed_flower_rep1</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Chondrolia Chalkidikis" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The biological replicates per tissue type were equimolarly mixed in 2 g final RNA pools. The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the EBNext Multiplex Oligos for Illumina (Set 1 and 2) kit (, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the QubitTM dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 5200 Fragment Analyzer (Agilent Technology Inc., CA, USA) according to DNF-473-33 - SS NGS Fragment 1-6000bp protocol, and the KAPA library Quantification kit (KAPA Biosystems, Cape Town, South Africa).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169828">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169828</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">CH_closed_flower</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>R1_2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192132" alias="R2_2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192132</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">R2_2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Chondrolia Chalkidikis: closed_flower_rep2</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Chondrolia Chalkidikis" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The biological replicates per tissue type were equimolarly mixed in 2 g final RNA pools. The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the EBNext Multiplex Oligos for Illumina (Set 1 and 2) kit (, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the QubitTM dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 5200 Fragment Analyzer (Agilent Technology Inc., CA, USA) according to DNF-473-33 - SS NGS Fragment 1-6000bp protocol, and the KAPA library Quantification kit (KAPA Biosystems, Cape Town, South Africa).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169828">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169828</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">CH_closed_flower</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>R2_2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192133" alias="R3_2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192133</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">R3_2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Chondrolia Chalkidikis: closed_flower_rep3</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Chondrolia Chalkidikis" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The biological replicates per tissue type were equimolarly mixed in 2 g final RNA pools. The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the EBNext Multiplex Oligos for Illumina (Set 1 and 2) kit (, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the QubitTM dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 5200 Fragment Analyzer (Agilent Technology Inc., CA, USA) according to DNF-473-33 - SS NGS Fragment 1-6000bp protocol, and the KAPA library Quantification kit (KAPA Biosystems, Cape Town, South Africa).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169828">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169828</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">CH_closed_flower</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>R3_2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192134" alias="R1_1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192134</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">R1_1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Chondrolia Chalkidikis: open_flower_rep1</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Chondrolia Chalkidikis" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The biological replicates per tissue type were equimolarly mixed in 2 g final RNA pools. The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the EBNext Multiplex Oligos for Illumina (Set 1 and 2) kit (, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the QubitTM dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 5200 Fragment Analyzer (Agilent Technology Inc., CA, USA) according to DNF-473-33 - SS NGS Fragment 1-6000bp protocol, and the KAPA library Quantification kit (KAPA Biosystems, Cape Town, South Africa).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169829">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169829</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">CH_open_flower</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>R1_1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192135" alias="R2_1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192135</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">R2_1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Chondrolia Chalkidikis: open_flower_rep2</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Chondrolia Chalkidikis" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The biological replicates per tissue type were equimolarly mixed in 2 g final RNA pools. The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the EBNext Multiplex Oligos for Illumina (Set 1 and 2) kit (, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the QubitTM dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 5200 Fragment Analyzer (Agilent Technology Inc., CA, USA) according to DNF-473-33 - SS NGS Fragment 1-6000bp protocol, and the KAPA library Quantification kit (KAPA Biosystems, Cape Town, South Africa).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169829">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169829</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">CH_open_flower</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>R2_1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192136" alias="R3_1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192136</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">R3_1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Chondrolia Chalkidikis: open_flower_rep3</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Chondrolia Chalkidikis" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The biological replicates per tissue type were equimolarly mixed in 2 g final RNA pools. The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the EBNext Multiplex Oligos for Illumina (Set 1 and 2) kit (, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the QubitTM dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 5200 Fragment Analyzer (Agilent Technology Inc., CA, USA) according to DNF-473-33 - SS NGS Fragment 1-6000bp protocol, and the KAPA library Quantification kit (KAPA Biosystems, Cape Town, South Africa).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169829">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169829</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">CH_open_flower</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>R3_1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192137" alias="R1_11">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192137</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">R1_11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Chondrolia Chalkidikis: root_rep1</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Chondrolia Chalkidikis" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The biological replicates per tissue type were equimolarly mixed in 2 g final RNA pools. The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the EBNext Multiplex Oligos for Illumina (Set 1 and 2) kit (, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the QubitTM dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 5200 Fragment Analyzer (Agilent Technology Inc., CA, USA) according to DNF-473-33 - SS NGS Fragment 1-6000bp protocol, and the KAPA library Quantification kit (KAPA Biosystems, Cape Town, South Africa).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169830">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169830</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">CH_root</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>R1_11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192138" alias="R2_11">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192138</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">R2_11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Chondrolia Chalkidikis: root_rep2</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Chondrolia Chalkidikis" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The biological replicates per tissue type were equimolarly mixed in 2 g final RNA pools. The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the EBNext Multiplex Oligos for Illumina (Set 1 and 2) kit (, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the QubitTM dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 5200 Fragment Analyzer (Agilent Technology Inc., CA, USA) according to DNF-473-33 - SS NGS Fragment 1-6000bp protocol, and the KAPA library Quantification kit (KAPA Biosystems, Cape Town, South Africa).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169830">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169830</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">CH_root</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>R2_11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192139" alias="R3_9">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192139</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">R3_9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Chondrolia Chalkidikis: young_leaf_rep3</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Chondrolia Chalkidikis" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The biological replicates per tissue type were equimolarly mixed in 2 g final RNA pools. The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the EBNext Multiplex Oligos for Illumina (Set 1 and 2) kit (, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the QubitTM dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 5200 Fragment Analyzer (Agilent Technology Inc., CA, USA) according to DNF-473-33 - SS NGS Fragment 1-6000bp protocol, and the KAPA library Quantification kit (KAPA Biosystems, Cape Town, South Africa).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169826">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169826</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">CH_young_leaf</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>R3_9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192140" alias="R3_11">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192140</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">R3_11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Chondrolia Chalkidikis: root_rep3</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Chondrolia Chalkidikis" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The biological replicates per tissue type were equimolarly mixed in 2 g final RNA pools. The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the EBNext Multiplex Oligos for Illumina (Set 1 and 2) kit (, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the QubitTM dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 5200 Fragment Analyzer (Agilent Technology Inc., CA, USA) according to DNF-473-33 - SS NGS Fragment 1-6000bp protocol, and the KAPA library Quantification kit (KAPA Biosystems, Cape Town, South Africa).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169830">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169830</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">CH_root</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>R3_11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192141" alias="R1_6">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192141</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">R1_6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Chondrolia Chalkidikis: stage2_fruit_rep1</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Chondrolia Chalkidikis" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The biological replicates per tissue type were equimolarly mixed in 2 g final RNA pools. The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the EBNext Multiplex Oligos for Illumina (Set 1 and 2) kit (, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the QubitTM dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 5200 Fragment Analyzer (Agilent Technology Inc., CA, USA) according to DNF-473-33 - SS NGS Fragment 1-6000bp protocol, and the KAPA library Quantification kit (KAPA Biosystems, Cape Town, South Africa).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169831">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169831</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">CH_stage2_fruit</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>R1_6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192142" alias="R2_6">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192142</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">R2_6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Chondrolia Chalkidikis: stage2_fruit_rep2</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Chondrolia Chalkidikis" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The biological replicates per tissue type were equimolarly mixed in 2 g final RNA pools. The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the EBNext Multiplex Oligos for Illumina (Set 1 and 2) kit (, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the QubitTM dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 5200 Fragment Analyzer (Agilent Technology Inc., CA, USA) according to DNF-473-33 - SS NGS Fragment 1-6000bp protocol, and the KAPA library Quantification kit (KAPA Biosystems, Cape Town, South Africa).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169831">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169831</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">CH_stage2_fruit</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>R2_6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192143" alias="R3_6">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192143</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">R3_6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Chondrolia Chalkidikis: stage2_fruit_rep3</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Chondrolia Chalkidikis" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The biological replicates per tissue type were equimolarly mixed in 2 g final RNA pools. The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the EBNext Multiplex Oligos for Illumina (Set 1 and 2) kit (, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the QubitTM dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 5200 Fragment Analyzer (Agilent Technology Inc., CA, USA) according to DNF-473-33 - SS NGS Fragment 1-6000bp protocol, and the KAPA library Quantification kit (KAPA Biosystems, Cape Town, South Africa).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169831">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169831</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">CH_stage2_fruit</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>R3_6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192144" alias="R1_3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192144</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">R1_3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Chondrolia Chalkidikis: stage2_endocarp_rep1</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Chondrolia Chalkidikis" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The biological replicates per tissue type were equimolarly mixed in 2 g final RNA pools. The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the EBNext Multiplex Oligos for Illumina (Set 1 and 2) kit (, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the QubitTM dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 5200 Fragment Analyzer (Agilent Technology Inc., CA, USA) according to DNF-473-33 - SS NGS Fragment 1-6000bp protocol, and the KAPA library Quantification kit (KAPA Biosystems, Cape Town, South Africa).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169832">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169832</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">CH_stage2_endocarp</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>R1_3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192145" alias="R2_3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192145</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">R2_3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Chondrolia Chalkidikis: stage2_endocarp_rep2</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Chondrolia Chalkidikis" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The biological replicates per tissue type were equimolarly mixed in 2 g final RNA pools. The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the EBNext Multiplex Oligos for Illumina (Set 1 and 2) kit (, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the QubitTM dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 5200 Fragment Analyzer (Agilent Technology Inc., CA, USA) according to DNF-473-33 - SS NGS Fragment 1-6000bp protocol, and the KAPA library Quantification kit (KAPA Biosystems, Cape Town, South Africa).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169832">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169832</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">CH_stage2_endocarp</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>R2_3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192146" alias="R3_3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192146</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">R3_3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Chondrolia Chalkidikis: stage2_endocarp_rep3</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Chondrolia Chalkidikis" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The biological replicates per tissue type were equimolarly mixed in 2 g final RNA pools. The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the EBNext Multiplex Oligos for Illumina (Set 1 and 2) kit (, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the QubitTM dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 5200 Fragment Analyzer (Agilent Technology Inc., CA, USA) according to DNF-473-33 - SS NGS Fragment 1-6000bp protocol, and the KAPA library Quantification kit (KAPA Biosystems, Cape Town, South Africa).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169832">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169832</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">CH_stage2_endocarp</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>R3_3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192147" alias="R1_7">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192147</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">R1_7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Chondrolia Chalkidikis: stage3_fruit_rep1</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Chondrolia Chalkidikis" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The biological replicates per tissue type were equimolarly mixed in 2 g final RNA pools. The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the EBNext Multiplex Oligos for Illumina (Set 1 and 2) kit (, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the QubitTM dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 5200 Fragment Analyzer (Agilent Technology Inc., CA, USA) according to DNF-473-33 - SS NGS Fragment 1-6000bp protocol, and the KAPA library Quantification kit (KAPA Biosystems, Cape Town, South Africa).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169833">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169833</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">CH_stage3_fruit</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>R1_7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192148" alias="R2_7">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192148</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">R2_7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Chondrolia Chalkidikis: stage3_fruit_rep2</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Chondrolia Chalkidikis" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The biological replicates per tissue type were equimolarly mixed in 2 g final RNA pools. The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the EBNext Multiplex Oligos for Illumina (Set 1 and 2) kit (, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the QubitTM dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 5200 Fragment Analyzer (Agilent Technology Inc., CA, USA) according to DNF-473-33 - SS NGS Fragment 1-6000bp protocol, and the KAPA library Quantification kit (KAPA Biosystems, Cape Town, South Africa).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169833">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169833</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">CH_stage3_fruit</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>R2_7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192149" alias="R3_7">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192149</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">R3_7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Chondrolia Chalkidikis: stage3_fruit_rep3</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Chondrolia Chalkidikis" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The biological replicates per tissue type were equimolarly mixed in 2 g final RNA pools. The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the EBNext Multiplex Oligos for Illumina (Set 1 and 2) kit (, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the QubitTM dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 5200 Fragment Analyzer (Agilent Technology Inc., CA, USA) according to DNF-473-33 - SS NGS Fragment 1-6000bp protocol, and the KAPA library Quantification kit (KAPA Biosystems, Cape Town, South Africa).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169833">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169833</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">CH_stage3_fruit</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>R3_7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192150" alias="R1_14">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192150</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">R1_14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Chondrolia Chalkidikis: young_shoot_rep1</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Chondrolia Chalkidikis" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The biological replicates per tissue type were equimolarly mixed in 2 g final RNA pools. The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the EBNext Multiplex Oligos for Illumina (Set 1 and 2) kit (, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the QubitTM dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 5200 Fragment Analyzer (Agilent Technology Inc., CA, USA) according to DNF-473-33 - SS NGS Fragment 1-6000bp protocol, and the KAPA library Quantification kit (KAPA Biosystems, Cape Town, South Africa).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169834">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169834</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">CH_young_shoot</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>R1_14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192151" alias="R1_4">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192151</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">R1_4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Chondrolia Chalkidikis: stage3_endocarp_rep1</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Chondrolia Chalkidikis" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The biological replicates per tissue type were equimolarly mixed in 2 g final RNA pools. The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the EBNext Multiplex Oligos for Illumina (Set 1 and 2) kit (, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the QubitTM dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 5200 Fragment Analyzer (Agilent Technology Inc., CA, USA) according to DNF-473-33 - SS NGS Fragment 1-6000bp protocol, and the KAPA library Quantification kit (KAPA Biosystems, Cape Town, South Africa).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169835">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169835</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">CH_stage3_endocarp</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>R1_4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192152" alias="R2_4">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192152</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">R2_4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Chondrolia Chalkidikis: stage3_endocarp_rep2</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Chondrolia Chalkidikis" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The biological replicates per tissue type were equimolarly mixed in 2 g final RNA pools. The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the EBNext Multiplex Oligos for Illumina (Set 1 and 2) kit (, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the QubitTM dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 5200 Fragment Analyzer (Agilent Technology Inc., CA, USA) according to DNF-473-33 - SS NGS Fragment 1-6000bp protocol, and the KAPA library Quantification kit (KAPA Biosystems, Cape Town, South Africa).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169835">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169835</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">CH_stage3_endocarp</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>R2_4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192153" alias="R3_4">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192153</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">R3_4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Chondrolia Chalkidikis: stage3_endocarp_rep3</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Chondrolia Chalkidikis" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The biological replicates per tissue type were equimolarly mixed in 2 g final RNA pools. The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the EBNext Multiplex Oligos for Illumina (Set 1 and 2) kit (, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the QubitTM dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 5200 Fragment Analyzer (Agilent Technology Inc., CA, USA) according to DNF-473-33 - SS NGS Fragment 1-6000bp protocol, and the KAPA library Quantification kit (KAPA Biosystems, Cape Town, South Africa).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169835">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169835</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">CH_stage3_endocarp</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>R3_4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192154" alias="R1_8">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192154</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">R1_8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Chondrolia Chalkidikis: stage4_fruit_rep1</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Chondrolia Chalkidikis" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The biological replicates per tissue type were equimolarly mixed in 2 g final RNA pools. The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the EBNext Multiplex Oligos for Illumina (Set 1 and 2) kit (, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the QubitTM dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 5200 Fragment Analyzer (Agilent Technology Inc., CA, USA) according to DNF-473-33 - SS NGS Fragment 1-6000bp protocol, and the KAPA library Quantification kit (KAPA Biosystems, Cape Town, South Africa).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169836">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169836</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">CH_stage4_fruit</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>R1_8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192155" alias="R2_8">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192155</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">R2_8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Chondrolia Chalkidikis: stage4_fruit_rep2</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Chondrolia Chalkidikis" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The biological replicates per tissue type were equimolarly mixed in 2 g final RNA pools. The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the EBNext Multiplex Oligos for Illumina (Set 1 and 2) kit (, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the QubitTM dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 5200 Fragment Analyzer (Agilent Technology Inc., CA, USA) according to DNF-473-33 - SS NGS Fragment 1-6000bp protocol, and the KAPA library Quantification kit (KAPA Biosystems, Cape Town, South Africa).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169836">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169836</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">CH_stage4_fruit</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>R2_8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192156" alias="R3_8">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192156</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">R3_8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Chondrolia Chalkidikis: stage4_fruit_rep3</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Chondrolia Chalkidikis" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The biological replicates per tissue type were equimolarly mixed in 2 g final RNA pools. The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the EBNext Multiplex Oligos for Illumina (Set 1 and 2) kit (, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the QubitTM dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 5200 Fragment Analyzer (Agilent Technology Inc., CA, USA) according to DNF-473-33 - SS NGS Fragment 1-6000bp protocol, and the KAPA library Quantification kit (KAPA Biosystems, Cape Town, South Africa).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169836">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169836</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">CH_stage4_fruit</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>R3_8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192157" alias="R1_5">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192157</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">R1_5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Chondrolia Chalkidikis: stage4_endocarp_rep1</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Chondrolia Chalkidikis" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The biological replicates per tissue type were equimolarly mixed in 2 g final RNA pools. The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the EBNext Multiplex Oligos for Illumina (Set 1 and 2) kit (, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the QubitTM dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 5200 Fragment Analyzer (Agilent Technology Inc., CA, USA) according to DNF-473-33 - SS NGS Fragment 1-6000bp protocol, and the KAPA library Quantification kit (KAPA Biosystems, Cape Town, South Africa).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169837">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169837</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">CH_stage4_endocarp</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>R1_5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192158" alias="R2_5">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192158</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">R2_5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Chondrolia Chalkidikis: stage4_endocarp_rep2</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Chondrolia Chalkidikis" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The biological replicates per tissue type were equimolarly mixed in 2 g final RNA pools. The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the EBNext Multiplex Oligos for Illumina (Set 1 and 2) kit (, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the QubitTM dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 5200 Fragment Analyzer (Agilent Technology Inc., CA, USA) according to DNF-473-33 - SS NGS Fragment 1-6000bp protocol, and the KAPA library Quantification kit (KAPA Biosystems, Cape Town, South Africa).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169837">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169837</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">CH_stage4_endocarp</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>R2_5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192159" alias="R3_5">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192159</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">R3_5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Chondrolia Chalkidikis: stage4_endocarp_rep3</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Chondrolia Chalkidikis" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The biological replicates per tissue type were equimolarly mixed in 2 g final RNA pools. The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the EBNext Multiplex Oligos for Illumina (Set 1 and 2) kit (, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the QubitTM dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 5200 Fragment Analyzer (Agilent Technology Inc., CA, USA) according to DNF-473-33 - SS NGS Fragment 1-6000bp protocol, and the KAPA library Quantification kit (KAPA Biosystems, Cape Town, South Africa).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169837">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169837</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">CH_stage4_endocarp</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>R3_5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192160" alias="R1_10">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192160</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">R1_10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Chondrolia Chalkidikis: stage4_stalk_rep1</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Chondrolia Chalkidikis" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The biological replicates per tissue type were equimolarly mixed in 2 g final RNA pools. The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the EBNext Multiplex Oligos for Illumina (Set 1 and 2) kit (, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the QubitTM dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 5200 Fragment Analyzer (Agilent Technology Inc., CA, USA) according to DNF-473-33 - SS NGS Fragment 1-6000bp protocol, and the KAPA library Quantification kit (KAPA Biosystems, Cape Town, South Africa).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169838">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169838</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">CH_stage4_stalk</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>R1_10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192161" alias="R2_14">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192161</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">R2_14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Chondrolia Chalkidikis: young_shoot_rep2</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Chondrolia Chalkidikis" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The biological replicates per tissue type were equimolarly mixed in 2 g final RNA pools. The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the EBNext Multiplex Oligos for Illumina (Set 1 and 2) kit (, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the QubitTM dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 5200 Fragment Analyzer (Agilent Technology Inc., CA, USA) according to DNF-473-33 - SS NGS Fragment 1-6000bp protocol, and the KAPA library Quantification kit (KAPA Biosystems, Cape Town, South Africa).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169834">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169834</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">CH_young_shoot</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>R2_14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192162" alias="R2_10">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192162</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">R2_10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Chondrolia Chalkidikis: stage4_stalk_rep2</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Chondrolia Chalkidikis" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The biological replicates per tissue type were equimolarly mixed in 2 g final RNA pools. The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the EBNext Multiplex Oligos for Illumina (Set 1 and 2) kit (, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the QubitTM dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 5200 Fragment Analyzer (Agilent Technology Inc., CA, USA) according to DNF-473-33 - SS NGS Fragment 1-6000bp protocol, and the KAPA library Quantification kit (KAPA Biosystems, Cape Town, South Africa).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169838">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169838</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">CH_stage4_stalk</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>R2_10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192163" alias="R3_10">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192163</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">R3_10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Chondrolia Chalkidikis: stage4_stalk_rep3</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Chondrolia Chalkidikis" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The biological replicates per tissue type were equimolarly mixed in 2 g final RNA pools. The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the EBNext Multiplex Oligos for Illumina (Set 1 and 2) kit (, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the QubitTM dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 5200 Fragment Analyzer (Agilent Technology Inc., CA, USA) according to DNF-473-33 - SS NGS Fragment 1-6000bp protocol, and the KAPA library Quantification kit (KAPA Biosystems, Cape Town, South Africa).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169838">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169838</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">CH_stage4_stalk</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>R3_10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192164" alias="Neb6609_A1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192164</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">Neb6609_A1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Koroneiki: young_leaf_rep1</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Koroneiki" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the NEBNext Multiplex Oligos for Illumina kit (NEB, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the Qubit dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 2100 Bioanalyzer (Agilent Technology Inc., CA, USA) using the Agilent High sensitivity DNA kit and the NEBnext library quant for Illumina kit ((NEB, Ipswich, MA, USA). Sequencing was performed in the NextSeq500 platform (Illumina, San Diego, CA, USA), using the NextSeq 500/550 High Output Kit v2.5 (300 Cycles), paired-end, 2x150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169839">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169839</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">KO_young_leaf</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Neb6609_A1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192165" alias="Neb6609_A2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192165</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">Neb6609_A2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Koroneiki: young_leaf_rep2</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Koroneiki" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the NEBNext Multiplex Oligos for Illumina kit (NEB, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the Qubit dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 2100 Bioanalyzer (Agilent Technology Inc., CA, USA) using the Agilent High sensitivity DNA kit and the NEBnext library quant for Illumina kit ((NEB, Ipswich, MA, USA). Sequencing was performed in the NextSeq500 platform (Illumina, San Diego, CA, USA), using the NextSeq 500/550 High Output Kit v2.5 (300 Cycles), paired-end, 2x150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169839">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169839</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">KO_young_leaf</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Neb6609_A2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192166" alias="Neb6609_A3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192166</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">Neb6609_A3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Koroneiki: young_leaf_rep3</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Koroneiki" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the NEBNext Multiplex Oligos for Illumina kit (NEB, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the Qubit dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 2100 Bioanalyzer (Agilent Technology Inc., CA, USA) using the Agilent High sensitivity DNA kit and the NEBnext library quant for Illumina kit ((NEB, Ipswich, MA, USA). Sequencing was performed in the NextSeq500 platform (Illumina, San Diego, CA, USA), using the NextSeq 500/550 High Output Kit v2.5 (300 Cycles), paired-end, 2x150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169839">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169839</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">KO_young_leaf</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Neb6609_A3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192167" alias="Neb6609_A4">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192167</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">Neb6609_A4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Koroneiki: young_shoot_rep1</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Koroneiki" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the NEBNext Multiplex Oligos for Illumina kit (NEB, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the Qubit dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 2100 Bioanalyzer (Agilent Technology Inc., CA, USA) using the Agilent High sensitivity DNA kit and the NEBnext library quant for Illumina kit ((NEB, Ipswich, MA, USA). Sequencing was performed in the NextSeq500 platform (Illumina, San Diego, CA, USA), using the NextSeq 500/550 High Output Kit v2.5 (300 Cycles), paired-end, 2x150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169840">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169840</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">KO_young_shoot</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Neb6609_A4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192168" alias="Neb6609_A5">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192168</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">Neb6609_A5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Koroneiki: young_shoot_rep2</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Koroneiki" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the NEBNext Multiplex Oligos for Illumina kit (NEB, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the Qubit dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 2100 Bioanalyzer (Agilent Technology Inc., CA, USA) using the Agilent High sensitivity DNA kit and the NEBnext library quant for Illumina kit ((NEB, Ipswich, MA, USA). Sequencing was performed in the NextSeq500 platform (Illumina, San Diego, CA, USA), using the NextSeq 500/550 High Output Kit v2.5 (300 Cycles), paired-end, 2x150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169840">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169840</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">KO_young_shoot</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Neb6609_A5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192169" alias="Neb6609_A6">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192169</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">Neb6609_A6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Koroneiki: young_shoot_rep3</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Koroneiki" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the NEBNext Multiplex Oligos for Illumina kit (NEB, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the Qubit dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 2100 Bioanalyzer (Agilent Technology Inc., CA, USA) using the Agilent High sensitivity DNA kit and the NEBnext library quant for Illumina kit ((NEB, Ipswich, MA, USA). Sequencing was performed in the NextSeq500 platform (Illumina, San Diego, CA, USA), using the NextSeq 500/550 High Output Kit v2.5 (300 Cycles), paired-end, 2x150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169840">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169840</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">KO_young_shoot</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Neb6609_A6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192170" alias="Neb6609_A7">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192170</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">Neb6609_A7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Koroneiki: mature_leaf_rep1</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Koroneiki" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the NEBNext Multiplex Oligos for Illumina kit (NEB, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the Qubit dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 2100 Bioanalyzer (Agilent Technology Inc., CA, USA) using the Agilent High sensitivity DNA kit and the NEBnext library quant for Illumina kit ((NEB, Ipswich, MA, USA). Sequencing was performed in the NextSeq500 platform (Illumina, San Diego, CA, USA), using the NextSeq 500/550 High Output Kit v2.5 (300 Cycles), paired-end, 2x150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169841">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169841</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">KO_mature_leaf</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Neb6609_A7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192171" alias="Neb6609_A8">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192171</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">Neb6609_A8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Koroneiki: mature_leaf_rep2</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Koroneiki" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the NEBNext Multiplex Oligos for Illumina kit (NEB, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the Qubit dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 2100 Bioanalyzer (Agilent Technology Inc., CA, USA) using the Agilent High sensitivity DNA kit and the NEBnext library quant for Illumina kit ((NEB, Ipswich, MA, USA). Sequencing was performed in the NextSeq500 platform (Illumina, San Diego, CA, USA), using the NextSeq 500/550 High Output Kit v2.5 (300 Cycles), paired-end, 2x150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169841">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169841</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">KO_mature_leaf</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Neb6609_A8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192172" alias="R3_14">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192172</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">R3_14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Chondrolia Chalkidikis: young_shoot_rep3</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Chondrolia Chalkidikis" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The biological replicates per tissue type were equimolarly mixed in 2 g final RNA pools. The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the EBNext Multiplex Oligos for Illumina (Set 1 and 2) kit (, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the QubitTM dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 5200 Fragment Analyzer (Agilent Technology Inc., CA, USA) according to DNF-473-33 - SS NGS Fragment 1-6000bp protocol, and the KAPA library Quantification kit (KAPA Biosystems, Cape Town, South Africa).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169834">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169834</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">CH_young_shoot</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>R3_14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192173" alias="Neb6609_A9">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192173</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">Neb6609_A9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Koroneiki: mature_leaf_rep3</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Koroneiki" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the NEBNext Multiplex Oligos for Illumina kit (NEB, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the Qubit dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 2100 Bioanalyzer (Agilent Technology Inc., CA, USA) using the Agilent High sensitivity DNA kit and the NEBnext library quant for Illumina kit ((NEB, Ipswich, MA, USA). Sequencing was performed in the NextSeq500 platform (Illumina, San Diego, CA, USA), using the NextSeq 500/550 High Output Kit v2.5 (300 Cycles), paired-end, 2x150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169841">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169841</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">KO_mature_leaf</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Neb6609_A9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192174" alias="Neb6609_A10">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192174</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">Neb6609_A10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Koroneiki: mature_shoot_rep1</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Koroneiki" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the NEBNext Multiplex Oligos for Illumina kit (NEB, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the Qubit dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 2100 Bioanalyzer (Agilent Technology Inc., CA, USA) using the Agilent High sensitivity DNA kit and the NEBnext library quant for Illumina kit ((NEB, Ipswich, MA, USA). Sequencing was performed in the NextSeq500 platform (Illumina, San Diego, CA, USA), using the NextSeq 500/550 High Output Kit v2.5 (300 Cycles), paired-end, 2x150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169842">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169842</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">KO_mature_shoot</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Neb6609_A10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192175" alias="Neb6609_A11">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192175</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">Neb6609_A11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Koroneiki: mature_shoot_rep2</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Koroneiki" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the NEBNext Multiplex Oligos for Illumina kit (NEB, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the Qubit dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 2100 Bioanalyzer (Agilent Technology Inc., CA, USA) using the Agilent High sensitivity DNA kit and the NEBnext library quant for Illumina kit ((NEB, Ipswich, MA, USA). Sequencing was performed in the NextSeq500 platform (Illumina, San Diego, CA, USA), using the NextSeq 500/550 High Output Kit v2.5 (300 Cycles), paired-end, 2x150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169842">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169842</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">KO_mature_shoot</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Neb6609_A11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192176" alias="Neb6609_A12">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192176</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">Neb6609_A12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Koroneiki: mature_shoot_rep3</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Koroneiki" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the NEBNext Multiplex Oligos for Illumina kit (NEB, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the Qubit dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 2100 Bioanalyzer (Agilent Technology Inc., CA, USA) using the Agilent High sensitivity DNA kit and the NEBnext library quant for Illumina kit ((NEB, Ipswich, MA, USA). Sequencing was performed in the NextSeq500 platform (Illumina, San Diego, CA, USA), using the NextSeq 500/550 High Output Kit v2.5 (300 Cycles), paired-end, 2x150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169842">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169842</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">KO_mature_shoot</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Neb6609_A12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192177" alias="Neb6609_1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192177</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">Neb6609_1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Koroneiki:closed_flower_rep1</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Koroneiki" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the NEBNext Multiplex Oligos for Illumina kit (NEB, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the Qubit dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 2100 Bioanalyzer (Agilent Technology Inc., CA, USA) using the Agilent High sensitivity DNA kit and the NEBnext library quant for Illumina kit ((NEB, Ipswich, MA, USA). Sequencing was performed in the NextSeq500 platform (Illumina, San Diego, CA, USA), using the NextSeq 500/550 High Output Kit v2.5 (300 Cycles), paired-end, 2x150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169843">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169843</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">KO_closed_flower</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Neb6609_1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192178" alias="Neb6609_2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192178</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">Neb6609_2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Koroneiki:closed_flower_rep2</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Koroneiki" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the NEBNext Multiplex Oligos for Illumina kit (NEB, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the Qubit dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 2100 Bioanalyzer (Agilent Technology Inc., CA, USA) using the Agilent High sensitivity DNA kit and the NEBnext library quant for Illumina kit ((NEB, Ipswich, MA, USA). Sequencing was performed in the NextSeq500 platform (Illumina, San Diego, CA, USA), using the NextSeq 500/550 High Output Kit v2.5 (300 Cycles), paired-end, 2x150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169843">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169843</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">KO_closed_flower</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Neb6609_2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192179" alias="Neb6609_3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192179</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">Neb6609_3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Koroneiki:closed_flower_rep3</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Koroneiki" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the NEBNext Multiplex Oligos for Illumina kit (NEB, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the Qubit dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 2100 Bioanalyzer (Agilent Technology Inc., CA, USA) using the Agilent High sensitivity DNA kit and the NEBnext library quant for Illumina kit ((NEB, Ipswich, MA, USA). Sequencing was performed in the NextSeq500 platform (Illumina, San Diego, CA, USA), using the NextSeq 500/550 High Output Kit v2.5 (300 Cycles), paired-end, 2x150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169843">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169843</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">KO_closed_flower</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Neb6609_3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192180" alias="Neb6609_4">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192180</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">Neb6609_4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Koroneiki:open_flower_rep1</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Koroneiki" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the NEBNext Multiplex Oligos for Illumina kit (NEB, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the Qubit dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 2100 Bioanalyzer (Agilent Technology Inc., CA, USA) using the Agilent High sensitivity DNA kit and the NEBnext library quant for Illumina kit ((NEB, Ipswich, MA, USA). Sequencing was performed in the NextSeq500 platform (Illumina, San Diego, CA, USA), using the NextSeq 500/550 High Output Kit v2.5 (300 Cycles), paired-end, 2x150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169844">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169844</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">KO_open_flower</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Neb6609_4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192181" alias="Neb6609_5">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192181</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">Neb6609_5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Koroneiki:open_flower_rep2</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Koroneiki" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the NEBNext Multiplex Oligos for Illumina kit (NEB, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the Qubit dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 2100 Bioanalyzer (Agilent Technology Inc., CA, USA) using the Agilent High sensitivity DNA kit and the NEBnext library quant for Illumina kit ((NEB, Ipswich, MA, USA). Sequencing was performed in the NextSeq500 platform (Illumina, San Diego, CA, USA), using the NextSeq 500/550 High Output Kit v2.5 (300 Cycles), paired-end, 2x150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169844">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169844</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">KO_open_flower</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Neb6609_5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192182" alias="Neb6609_6">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192182</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">Neb6609_6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Koroneiki:open_flower_rep3</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Koroneiki" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the NEBNext Multiplex Oligos for Illumina kit (NEB, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the Qubit dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 2100 Bioanalyzer (Agilent Technology Inc., CA, USA) using the Agilent High sensitivity DNA kit and the NEBnext library quant for Illumina kit ((NEB, Ipswich, MA, USA). Sequencing was performed in the NextSeq500 platform (Illumina, San Diego, CA, USA), using the NextSeq 500/550 High Output Kit v2.5 (300 Cycles), paired-end, 2x150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169844">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169844</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">KO_open_flower</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Neb6609_6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192183" alias="R1_12">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192183</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">R1_12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Chondrolia Chalkidikis: mature_leaf_rep1</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Chondrolia Chalkidikis" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The biological replicates per tissue type were equimolarly mixed in 2 g final RNA pools. The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the EBNext Multiplex Oligos for Illumina (Set 1 and 2) kit (, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the QubitTM dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 5200 Fragment Analyzer (Agilent Technology Inc., CA, USA) according to DNF-473-33 - SS NGS Fragment 1-6000bp protocol, and the KAPA library Quantification kit (KAPA Biosystems, Cape Town, South Africa).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169846">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169846</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">CH_mature_leaf</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>R1_12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192184" alias="Neb6609_7">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192184</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">Neb6609_7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Koroneiki:root_rep1</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Koroneiki" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the NEBNext Multiplex Oligos for Illumina kit (NEB, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the Qubit dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 2100 Bioanalyzer (Agilent Technology Inc., CA, USA) using the Agilent High sensitivity DNA kit and the NEBnext library quant for Illumina kit ((NEB, Ipswich, MA, USA). Sequencing was performed in the NextSeq500 platform (Illumina, San Diego, CA, USA), using the NextSeq 500/550 High Output Kit v2.5 (300 Cycles), paired-end, 2x150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169845">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169845</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">KO_root</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Neb6609_7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192185" alias="Neb6609_8">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192185</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">Neb6609_8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Koroneiki:root_rep2</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Koroneiki" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the NEBNext Multiplex Oligos for Illumina kit (NEB, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the Qubit dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 2100 Bioanalyzer (Agilent Technology Inc., CA, USA) using the Agilent High sensitivity DNA kit and the NEBnext library quant for Illumina kit ((NEB, Ipswich, MA, USA). Sequencing was performed in the NextSeq500 platform (Illumina, San Diego, CA, USA), using the NextSeq 500/550 High Output Kit v2.5 (300 Cycles), paired-end, 2x150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169845">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169845</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">KO_root</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Neb6609_8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192186" alias="Neb6609_9">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192186</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">Neb6609_9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Koroneiki:root_rep3</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Koroneiki" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the NEBNext Multiplex Oligos for Illumina kit (NEB, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the Qubit dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 2100 Bioanalyzer (Agilent Technology Inc., CA, USA) using the Agilent High sensitivity DNA kit and the NEBnext library quant for Illumina kit ((NEB, Ipswich, MA, USA). Sequencing was performed in the NextSeq500 platform (Illumina, San Diego, CA, USA), using the NextSeq 500/550 High Output Kit v2.5 (300 Cycles), paired-end, 2x150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169845">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169845</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">KO_root</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Neb6609_9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192187" alias="Neb6609_10">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192187</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">Neb6609_10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Koroneiki:stage_2_fruit_rep1</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Koroneiki" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the NEBNext Multiplex Oligos for Illumina kit (NEB, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the Qubit dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 2100 Bioanalyzer (Agilent Technology Inc., CA, USA) using the Agilent High sensitivity DNA kit and the NEBnext library quant for Illumina kit ((NEB, Ipswich, MA, USA). Sequencing was performed in the NextSeq500 platform (Illumina, San Diego, CA, USA), using the NextSeq 500/550 High Output Kit v2.5 (300 Cycles), paired-end, 2x150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169847">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169847</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">KO_stage2_fruit</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Neb6609_10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192188" alias="Neb6609_11">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192188</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">Neb6609_11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Koroneiki:stage_2_fruit_rep2</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Koroneiki" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the NEBNext Multiplex Oligos for Illumina kit (NEB, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the Qubit dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 2100 Bioanalyzer (Agilent Technology Inc., CA, USA) using the Agilent High sensitivity DNA kit and the NEBnext library quant for Illumina kit ((NEB, Ipswich, MA, USA). Sequencing was performed in the NextSeq500 platform (Illumina, San Diego, CA, USA), using the NextSeq 500/550 High Output Kit v2.5 (300 Cycles), paired-end, 2x150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169847">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169847</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">KO_stage2_fruit</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Neb6609_11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192189" alias="Neb6609_12">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192189</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">Neb6609_12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Koroneiki:stage_2_fruit_rep3</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Koroneiki" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the NEBNext Multiplex Oligos for Illumina kit (NEB, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the Qubit dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 2100 Bioanalyzer (Agilent Technology Inc., CA, USA) using the Agilent High sensitivity DNA kit and the NEBnext library quant for Illumina kit ((NEB, Ipswich, MA, USA). Sequencing was performed in the NextSeq500 platform (Illumina, San Diego, CA, USA), using the NextSeq 500/550 High Output Kit v2.5 (300 Cycles), paired-end, 2x150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169847">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169847</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">KO_stage2_fruit</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Neb6609_12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192190" alias="NNeb6609_C1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192190</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">NNeb6609_C1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Koroneiki:stage_2_endocarp_rep1</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Koroneiki" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the NEBNext Multiplex Oligos for Illumina kit (NEB, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the Qubit dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 2100 Bioanalyzer (Agilent Technology Inc., CA, USA) using the Agilent High sensitivity DNA kit and the NEBnext library quant for Illumina kit ((NEB, Ipswich, MA, USA). Sequencing was performed in the NextSeq500 platform (Illumina, San Diego, CA, USA), using the NextSeq 500/550 High Output Kit v2.5 (300 Cycles), paired-end, 2x150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169848">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169848</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">KO_stage2_endocarp</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NNeb6609_C1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192191" alias="Neb6609_C2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192191</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">Neb6609_C2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Koroneiki:stage_2_endocarp_rep2</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Koroneiki" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the NEBNext Multiplex Oligos for Illumina kit (NEB, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the Qubit dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 2100 Bioanalyzer (Agilent Technology Inc., CA, USA) using the Agilent High sensitivity DNA kit and the NEBnext library quant for Illumina kit ((NEB, Ipswich, MA, USA). Sequencing was performed in the NextSeq500 platform (Illumina, San Diego, CA, USA), using the NextSeq 500/550 High Output Kit v2.5 (300 Cycles), paired-end, 2x150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169848">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169848</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">KO_stage2_endocarp</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Neb6609_C2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192192" alias="Neb6609_C3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192192</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">Neb6609_C3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Koroneiki:stage_2_endocarp_rep3</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Koroneiki" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the NEBNext Multiplex Oligos for Illumina kit (NEB, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the Qubit dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 2100 Bioanalyzer (Agilent Technology Inc., CA, USA) using the Agilent High sensitivity DNA kit and the NEBnext library quant for Illumina kit ((NEB, Ipswich, MA, USA). Sequencing was performed in the NextSeq500 platform (Illumina, San Diego, CA, USA), using the NextSeq 500/550 High Output Kit v2.5 (300 Cycles), paired-end, 2x150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169848">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169848</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">KO_stage2_endocarp</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Neb6609_C3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192193" alias="Neb6609_C4">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192193</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">Neb6609_C4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Koroneiki:stage_3_fruit_rep1</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Koroneiki" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the NEBNext Multiplex Oligos for Illumina kit (NEB, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the Qubit dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 2100 Bioanalyzer (Agilent Technology Inc., CA, USA) using the Agilent High sensitivity DNA kit and the NEBnext library quant for Illumina kit ((NEB, Ipswich, MA, USA). Sequencing was performed in the NextSeq500 platform (Illumina, San Diego, CA, USA), using the NextSeq 500/550 High Output Kit v2.5 (300 Cycles), paired-end, 2x150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169849">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169849</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">KO_stage3_fruit</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Neb6609_C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192194" alias="R2_12">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192194</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">R2_12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Chondrolia Chalkidikis: mature_leaf_rep2</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Chondrolia Chalkidikis" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The biological replicates per tissue type were equimolarly mixed in 2 g final RNA pools. The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the EBNext Multiplex Oligos for Illumina (Set 1 and 2) kit (, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the QubitTM dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 5200 Fragment Analyzer (Agilent Technology Inc., CA, USA) according to DNF-473-33 - SS NGS Fragment 1-6000bp protocol, and the KAPA library Quantification kit (KAPA Biosystems, Cape Town, South Africa).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169846">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169846</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">CH_mature_leaf</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>R2_12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192195" alias="Neb6609_C5">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192195</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">Neb6609_C5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Koroneiki:stage_3_fruit_rep2</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Koroneiki" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the NEBNext Multiplex Oligos for Illumina kit (NEB, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the Qubit dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 2100 Bioanalyzer (Agilent Technology Inc., CA, USA) using the Agilent High sensitivity DNA kit and the NEBnext library quant for Illumina kit ((NEB, Ipswich, MA, USA). Sequencing was performed in the NextSeq500 platform (Illumina, San Diego, CA, USA), using the NextSeq 500/550 High Output Kit v2.5 (300 Cycles), paired-end, 2x150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169849">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169849</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">KO_stage3_fruit</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Neb6609_C5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192196" alias="Neb6609_C6">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192196</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">Neb6609_C6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Koroneiki:stage_3_fruit_rep3</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Koroneiki" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the NEBNext Multiplex Oligos for Illumina kit (NEB, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the Qubit dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 2100 Bioanalyzer (Agilent Technology Inc., CA, USA) using the Agilent High sensitivity DNA kit and the NEBnext library quant for Illumina kit ((NEB, Ipswich, MA, USA). Sequencing was performed in the NextSeq500 platform (Illumina, San Diego, CA, USA), using the NextSeq 500/550 High Output Kit v2.5 (300 Cycles), paired-end, 2x150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169849">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169849</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">KO_stage3_fruit</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Neb6609_C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192197" alias="Neb6609_C7">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192197</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">Neb6609_C7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Koroneiki:stage_3_endocarp_rep1</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Koroneiki" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the NEBNext Multiplex Oligos for Illumina kit (NEB, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the Qubit dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 2100 Bioanalyzer (Agilent Technology Inc., CA, USA) using the Agilent High sensitivity DNA kit and the NEBnext library quant for Illumina kit ((NEB, Ipswich, MA, USA). Sequencing was performed in the NextSeq500 platform (Illumina, San Diego, CA, USA), using the NextSeq 500/550 High Output Kit v2.5 (300 Cycles), paired-end, 2x150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169850">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169850</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">KO_stage3_endocarp</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Neb6609_C7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192198" alias="Neb6609_C8">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192198</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">Neb6609_C8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Koroneiki:stage_3_endocarp_rep2</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Koroneiki" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the NEBNext Multiplex Oligos for Illumina kit (NEB, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the Qubit dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 2100 Bioanalyzer (Agilent Technology Inc., CA, USA) using the Agilent High sensitivity DNA kit and the NEBnext library quant for Illumina kit ((NEB, Ipswich, MA, USA). Sequencing was performed in the NextSeq500 platform (Illumina, San Diego, CA, USA), using the NextSeq 500/550 High Output Kit v2.5 (300 Cycles), paired-end, 2x150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169850">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169850</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">KO_stage3_endocarp</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Neb6609_C8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192199" alias="Neb6609_C9">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192199</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">Neb6609_C9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Koroneiki:stage_3_endocarp_rep3</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Koroneiki" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the NEBNext Multiplex Oligos for Illumina kit (NEB, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the Qubit dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 2100 Bioanalyzer (Agilent Technology Inc., CA, USA) using the Agilent High sensitivity DNA kit and the NEBnext library quant for Illumina kit ((NEB, Ipswich, MA, USA). Sequencing was performed in the NextSeq500 platform (Illumina, San Diego, CA, USA), using the NextSeq 500/550 High Output Kit v2.5 (300 Cycles), paired-end, 2x150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169850">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169850</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">KO_stage3_endocarp</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Neb6609_C9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192200" alias="E2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192200</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">E2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Koroneiki:stage_4_fruit_rep1</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Koroneiki" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the NEBNext Multiplex Oligos for Illumina kit (NEB, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the Qubit dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 2100 Bioanalyzer (Agilent Technology Inc., CA, USA) using the Agilent High sensitivity DNA kit and the NEBnext library quant for Illumina kit ((NEB, Ipswich, MA, USA). Sequencing was performed in the NextSeq500 platform (Illumina, San Diego, CA, USA), using the NextSeq 500/550 High Output Kit v2.5 (300 Cycles), paired-end, 2x150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169851">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169851</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">KO_stage4_fruit</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>E2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192201" alias="E3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192201</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">E3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Koroneiki:stage_4_fruit_rep2</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Koroneiki" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the NEBNext Multiplex Oligos for Illumina kit (NEB, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the Qubit dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 2100 Bioanalyzer (Agilent Technology Inc., CA, USA) using the Agilent High sensitivity DNA kit and the NEBnext library quant for Illumina kit ((NEB, Ipswich, MA, USA). Sequencing was performed in the NextSeq500 platform (Illumina, San Diego, CA, USA), using the NextSeq 500/550 High Output Kit v2.5 (300 Cycles), paired-end, 2x150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169851">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169851</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">KO_stage4_fruit</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>E3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192202" alias="E5">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192202</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">E5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Koroneiki:stage_4_fruit_rep3</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Koroneiki" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the NEBNext Multiplex Oligos for Illumina kit (NEB, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the Qubit dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 2100 Bioanalyzer (Agilent Technology Inc., CA, USA) using the Agilent High sensitivity DNA kit and the NEBnext library quant for Illumina kit ((NEB, Ipswich, MA, USA). Sequencing was performed in the NextSeq500 platform (Illumina, San Diego, CA, USA), using the NextSeq 500/550 High Output Kit v2.5 (300 Cycles), paired-end, 2x150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169851">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169851</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">KO_stage4_fruit</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>E5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192203" alias="E6">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192203</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">E6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Koroneiki:stage_4_endocarp_rep1</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Koroneiki" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the NEBNext Multiplex Oligos for Illumina kit (NEB, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the Qubit dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 2100 Bioanalyzer (Agilent Technology Inc., CA, USA) using the Agilent High sensitivity DNA kit and the NEBnext library quant for Illumina kit ((NEB, Ipswich, MA, USA). Sequencing was performed in the NextSeq500 platform (Illumina, San Diego, CA, USA), using the NextSeq 500/550 High Output Kit v2.5 (300 Cycles), paired-end, 2x150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169852">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169852</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">KO_stage4_endocarp</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>E6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192204" alias="E7">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192204</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">E7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Koroneiki:stage_4_endocarp_rep2</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Koroneiki" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the NEBNext Multiplex Oligos for Illumina kit (NEB, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the Qubit dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 2100 Bioanalyzer (Agilent Technology Inc., CA, USA) using the Agilent High sensitivity DNA kit and the NEBnext library quant for Illumina kit ((NEB, Ipswich, MA, USA). Sequencing was performed in the NextSeq500 platform (Illumina, San Diego, CA, USA), using the NextSeq 500/550 High Output Kit v2.5 (300 Cycles), paired-end, 2x150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169852">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169852</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">KO_stage4_endocarp</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>E7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192205" alias="R3_12">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192205</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">R3_12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Chondrolia Chalkidikis: mature_leaf_rep3</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Chondrolia Chalkidikis" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The biological replicates per tissue type were equimolarly mixed in 2 g final RNA pools. The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the EBNext Multiplex Oligos for Illumina (Set 1 and 2) kit (, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the QubitTM dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 5200 Fragment Analyzer (Agilent Technology Inc., CA, USA) according to DNF-473-33 - SS NGS Fragment 1-6000bp protocol, and the KAPA library Quantification kit (KAPA Biosystems, Cape Town, South Africa).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169846">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169846</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">CH_mature_leaf</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>R3_12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192206" alias="E11">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192206</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">E11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Koroneiki:stage_4_endocarp_rep3</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Koroneiki" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the NEBNext Multiplex Oligos for Illumina kit (NEB, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the Qubit dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 2100 Bioanalyzer (Agilent Technology Inc., CA, USA) using the Agilent High sensitivity DNA kit and the NEBnext library quant for Illumina kit ((NEB, Ipswich, MA, USA). Sequencing was performed in the NextSeq500 platform (Illumina, San Diego, CA, USA), using the NextSeq 500/550 High Output Kit v2.5 (300 Cycles), paired-end, 2x150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169852">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169852</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">KO_stage4_endocarp</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>E11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192207" alias="E12">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192207</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">E12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Koroneiki:stage_4_stalk_rep1</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Koroneiki" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the NEBNext Multiplex Oligos for Illumina kit (NEB, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the Qubit dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 2100 Bioanalyzer (Agilent Technology Inc., CA, USA) using the Agilent High sensitivity DNA kit and the NEBnext library quant for Illumina kit ((NEB, Ipswich, MA, USA). Sequencing was performed in the NextSeq500 platform (Illumina, San Diego, CA, USA), using the NextSeq 500/550 High Output Kit v2.5 (300 Cycles), paired-end, 2x150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169853">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169853</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">KO_stage4_stalk</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>E12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192208" alias="D1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192208</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">D1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Koroneiki:stage_4_stalk_rep2</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Koroneiki" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the NEBNext Multiplex Oligos for Illumina kit (NEB, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the Qubit dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 2100 Bioanalyzer (Agilent Technology Inc., CA, USA) using the Agilent High sensitivity DNA kit and the NEBnext library quant for Illumina kit ((NEB, Ipswich, MA, USA). Sequencing was performed in the NextSeq500 platform (Illumina, San Diego, CA, USA), using the NextSeq 500/550 High Output Kit v2.5 (300 Cycles), paired-end, 2x150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169853">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169853</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">KO_stage4_stalk</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192209" alias="F12">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192209</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">F12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Koroneiki:stage_4_stalk_rep3</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Koroneiki" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the NEBNext Multiplex Oligos for Illumina kit (NEB, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the Qubit dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 2100 Bioanalyzer (Agilent Technology Inc., CA, USA) using the Agilent High sensitivity DNA kit and the NEBnext library quant for Illumina kit ((NEB, Ipswich, MA, USA). Sequencing was performed in the NextSeq500 platform (Illumina, San Diego, CA, USA), using the NextSeq 500/550 High Output Kit v2.5 (300 Cycles), paired-end, 2x150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169853">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169853</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">KO_stage4_stalk</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>F12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12192210" alias="R1_13">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12192210</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9992605">R1_13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Chondrolia Chalkidikis: mature_shoot_rep1</TITLE>
    <STUDY_REF accession="SRP337118">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP337118</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9992605">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from fresh tissue material for 14 tissue types of the olive variety "Chondrolia Chalkidikis" in three biological replicates, using the Monarch Total RNA Miniprep Kit (NEB, Ipswich, MA, USA). The biological replicates per tissue type were equimolarly mixed in 2 g final RNA pools. The RNA libraries were prepared using the NeBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) and library indexing was performed using the EBNext Multiplex Oligos for Illumina (Set 1 and 2) kit (, Ipswich, MA, USA), according to the manufacturers instructions. RNA library quantity and quality were assessed using the QubitTM dsDNA HS Assay Kit (Invitrogen, Oregon, USA), the 5200 Fragment Analyzer (Agilent Technology Inc., CA, USA) according to DNF-473-33 - SS NGS Fragment 1-6000bp protocol, and the KAPA library Quantification kit (KAPA Biosystems, Cape Town, South Africa).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10169827">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10169827</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|oleagenome@gmail.com">CH_mature_shoot</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>R1_13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
