<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX13456096" alias="GSM5742750_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456096</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742750_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742750: S6_rep1_input; Oryza sativa; RIP-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353940">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353940</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742750</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742750</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456097" alias="GSM5742751_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456097</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742751_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742751: S6_rep1_RIP; Oryza sativa; RIP-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353941">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353941</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742751</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742751</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456098" alias="GSM5742752_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456098</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742752_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742752: S6_rep2_input; Oryza sativa; RIP-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353942">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353942</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742752</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742752</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456099" alias="GSM5742753_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456099</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742753_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742753: S6_rep2_RIP; Oryza sativa; RIP-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353943">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353943</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742753</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742753</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456100" alias="GSM5742754_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456100</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742754_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742754: S6_rep3_input; Oryza sativa; RIP-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353944">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353944</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742754</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742754</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456101" alias="GSM5742755_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456101</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742755_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742755: S6_rep3_RIP; Oryza sativa; RIP-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353945">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353945</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742755</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742755</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456102" alias="GSM5742756_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456102</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742756_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742756: S8_rep1_input; Oryza sativa; RIP-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353946">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353946</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742756</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742756</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456103" alias="GSM5742757_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456103</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742757_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742757: S8_rep1_RIP; Oryza sativa; RIP-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353947">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353947</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742757</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742757</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456104" alias="GSM5742758_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456104</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742758_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742758: S8_rep2_input; Oryza sativa; RIP-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353948">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353948</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742758</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742758</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456105" alias="GSM5742759_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456105</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742759_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742759: S8_rep2_RIP; Oryza sativa; RIP-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353949">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353949</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742759</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742759</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456106" alias="GSM5742760_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456106</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742760_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742760: S8_rep3_input; Oryza sativa; RIP-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353950">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353950</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742760</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742760</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456107" alias="GSM5742761_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456107</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742761_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742761: S8_rep3_RIP; Oryza sativa; RIP-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353951">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353951</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742761</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742761</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456108" alias="GSM5742762_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456108</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742762_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742762: S9_rep1_input; Oryza sativa; RIP-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353952">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353952</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742762</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742762</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456109" alias="GSM5742763_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456109</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742763_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742763: S9_rep1_RIP; Oryza sativa; RIP-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353953">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353953</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742763</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742763</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456110" alias="GSM5742764_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456110</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742764_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742764: S9_rep2_input; Oryza sativa; RIP-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353954">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353954</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742764</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742764</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456111" alias="GSM5742765_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456111</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742765_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742765: S9_rep2_RIP; Oryza sativa; RIP-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353955">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353955</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742765</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742765</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456112" alias="GSM5742766_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456112</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742766_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742766: S9_rep3_input; Oryza sativa; RIP-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353956">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353956</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742766</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742766</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456113" alias="GSM5742767_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456113</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742767_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742767: S9_rep3_RIP; Oryza sativa; RIP-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353957">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353957</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742767</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742767</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456114" alias="GSM5742678_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456114</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742678_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742678: ago1d_s6_LT_RNAseq_rep1; Oryza sativa; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353958">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353958</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742678</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742678</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456115" alias="GSM5742679_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456115</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742679_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742679: ago1d_s6_LT_RNAseq_rep2; Oryza sativa; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353959">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353959</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742679</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742679</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456116" alias="GSM5742680_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456116</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742680_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742680: ago1d_s6_LT_RNAseq_rep3; Oryza sativa; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353960">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353960</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742680</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742680</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456117" alias="GSM5742681_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456117</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742681_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742681: ago1d_s6_NT_RNAseq_rep1; Oryza sativa; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353961">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353961</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742681</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742681</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456118" alias="GSM5742682_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456118</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742682_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742682: ago1d_s6_NT_RNAseq_rep2; Oryza sativa; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353962">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353962</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742682</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742682</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456119" alias="GSM5742683_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456119</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742683_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742683: ago1d_s6_NT_RNAseq_rep3; Oryza sativa; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353963">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353963</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742683</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742683</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456120" alias="GSM5742684_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456120</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742684_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742684: wt_s6_LT_RNAseq_rep1; Oryza sativa; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353964">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353964</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742684</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742684</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456121" alias="GSM5742685_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456121</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742685_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742685: wt_s6_LT_RNAseq_rep2; Oryza sativa; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353965">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353965</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742685</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742685</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456122" alias="GSM5742686_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456122</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742686_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742686: wt_s6_LT_RNAseq_rep3; Oryza sativa; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353966">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353966</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742686</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742686</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456123" alias="GSM5742687_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456123</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742687_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742687: wt_s6_NT_RNAseq_rep1; Oryza sativa; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353967">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353967</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742687</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742687</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456124" alias="GSM5742688_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456124</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742688_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742688: wt_s6_NT_RNAseq_rep2; Oryza sativa; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353968">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353968</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742688</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742688</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456125" alias="GSM5742689_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456125</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742689_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742689: wt_s6_NT_RNAseq_rep3; Oryza sativa; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353969">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353969</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742689</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742689</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456126" alias="GSM5742690_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456126</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742690_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742690: ago1d_s8_LT_RNAseq_rep1; Oryza sativa; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353970">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353970</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742690</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742690</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456127" alias="GSM5742691_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456127</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742691_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742691: ago1d_s8_LT_RNAseq_rep2; Oryza sativa; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353971">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353971</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742691</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742691</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456128" alias="GSM5742692_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456128</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742692_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742692: ago1d_s8_LT_RNAseq_rep3; Oryza sativa; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353972">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353972</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742692</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742692</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456129" alias="GSM5742693_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456129</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742693_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742693: ago1d_s8_NT_RNAseq_rep1; Oryza sativa; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353973">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353973</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742693</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742693</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456130" alias="GSM5742694_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456130</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742694_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742694: ago1d_s8_NT_RNAseq_rep2; Oryza sativa; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353974">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353974</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742694</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742694</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456131" alias="GSM5742695_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456131</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742695_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742695: ago1d_s8_NT_RNAseq_rep3; Oryza sativa; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353975">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353975</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742695</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742695</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456132" alias="GSM5742696_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456132</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742696_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742696: wt_s8_LT_RNAseq_rep1; Oryza sativa; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353976">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353976</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742696</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742696</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456133" alias="GSM5742697_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456133</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742697_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742697: wt_s8_LT_RNAseq_rep2; Oryza sativa; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353977">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353977</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742697</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742697</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456134" alias="GSM5742698_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456134</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742698_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742698: wt_s8_LT_RNAseq_rep3; Oryza sativa; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353978">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353978</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742698</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742698</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456135" alias="GSM5742699_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456135</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742699_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742699: wt_s8_NT_RNAseq_rep1; Oryza sativa; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353979">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353979</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742699</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742699</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456136" alias="GSM5742700_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456136</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742700_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742700: wt_s8_NT_RNAseq_rep2; Oryza sativa; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353980">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353980</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742700</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742700</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456137" alias="GSM5742701_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456137</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742701_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742701: wt_s8_NT_RNAseq_rep3; Oryza sativa; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353981">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353981</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742701</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742701</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456138" alias="GSM5742702_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456138</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742702_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742702: ago1d_s9_LT_RNAseq_rep1; Oryza sativa; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353982">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353982</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742702</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742702</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456139" alias="GSM5742703_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456139</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742703_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742703: ago1d_s9_LT_RNAseq_rep2; Oryza sativa; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353983">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353983</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742703</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742703</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456140" alias="GSM5742704_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456140</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742704_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742704: ago1d_s9_LT_RNAseq_rep3; Oryza sativa; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353984">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353984</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742704</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742704</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456141" alias="GSM5742705_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456141</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742705_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742705: ago1d_s9_NT_RNAseq_rep1; Oryza sativa; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353985">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353985</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742705</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742705</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456142" alias="GSM5742706_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456142</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742706_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742706: ago1d_s9_NT_RNAseq_rep2; Oryza sativa; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353986">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353986</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742706</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742706</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456143" alias="GSM5742707_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456143</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742707_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742707: ago1d_s9_NT_RNAseq_rep3; Oryza sativa; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353987">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353987</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742707</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742707</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456144" alias="GSM5742708_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456144</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742708_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742708: wt_s9_LT_RNAseq_rep1; Oryza sativa; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353988">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353988</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742708</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742708</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456145" alias="GSM5742709_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456145</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742709_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742709: wt_s9_LT_RNAseq_rep2; Oryza sativa; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353989">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353989</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742709</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742709</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456146" alias="GSM5742710_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456146</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742710_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742710: wt_s9_LT_RNAseq_rep3; Oryza sativa; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353990">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353990</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742710</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742710</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456147" alias="GSM5742711_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456147</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742711_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742711: wt_s9_NT_RNAseq_rep1; Oryza sativa; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353991">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353991</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742711</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742711</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456148" alias="GSM5742712_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456148</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742712_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742712: wt_s9_NT_RNAseq_rep2; Oryza sativa; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353992">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353992</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742712</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742712</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456149" alias="GSM5742713_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456149</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742713_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742713: wt_s9_NT_RNAseq_rep3; Oryza sativa; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353993">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353993</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742713</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742713</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456150" alias="GSM5742714_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456150</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742714_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742714: ago1d_s6_LT_sRNAseq_rep1; Oryza sativa; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353994">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353994</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742714</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742714</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456151" alias="GSM5742715_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456151</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742715_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742715: ago1d_s6_LT_sRNAseq_rep2; Oryza sativa; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353995">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353995</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742715</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742715</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456152" alias="GSM5742716_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456152</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742716_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742716: ago1d_s6_LT_sRNAseq_rep3; Oryza sativa; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353996">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353996</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742716</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742716</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456153" alias="GSM5742717_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456153</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742717_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742717: ago1d_s6_NT_sRNAseq_rep1; Oryza sativa; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353997">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353997</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742717</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742717</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456154" alias="GSM5742718_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456154</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742718_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742718: ago1d_s6_NT_sRNAseq_rep2; Oryza sativa; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353998">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353998</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742718</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742718</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456155" alias="GSM5742719_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456155</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742719_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742719: ago1d_s6_NT_sRNAseq_rep3; Oryza sativa; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11353999">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11353999</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742719</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742719</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456156" alias="GSM5742720_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456156</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742720_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742720: wt_s6_LT_sRNAseq_rep1; Oryza sativa; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11354000">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11354000</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742720</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742720</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456157" alias="GSM5742721_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456157</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742721_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742721: wt_s6_LT_sRNAseq_rep2; Oryza sativa; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11354001">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11354001</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742721</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742721</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456158" alias="GSM5742722_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456158</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742722_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742722: wt_s6_LT_sRNAseq_rep3; Oryza sativa; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11354002">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11354002</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742722</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742722</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456159" alias="GSM5742723_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456159</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742723_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742723: wt_s6_NT_sRNAseq_rep1; Oryza sativa; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11354003">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11354003</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742723</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742723</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456160" alias="GSM5742724_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456160</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742724_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742724: wt_s6_NT_sRNAseq_rep2; Oryza sativa; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11354004">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11354004</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742724</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742724</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456161" alias="GSM5742725_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456161</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742725_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742725: wt_s6_NT_sRNAseq_rep3; Oryza sativa; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11354005">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11354005</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742725</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742725</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456162" alias="GSM5742726_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456162</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742726_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742726: ago1d_s8_LT_sRNAseq_rep1; Oryza sativa; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11354006">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11354006</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742726</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742726</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456163" alias="GSM5742727_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456163</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742727_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742727: ago1d_s8_LT_sRNAseq_rep2; Oryza sativa; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11354007">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11354007</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742727</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742727</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456164" alias="GSM5742728_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456164</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742728_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742728: ago1d_s8_LT_sRNAseq_rep3; Oryza sativa; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11354008">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11354008</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742728</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742728</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456165" alias="GSM5742729_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456165</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742729_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742729: ago1d_s8_NT_sRNAseq_rep1; Oryza sativa; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11354009">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11354009</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742729</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742729</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456166" alias="GSM5742730_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456166</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742730_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742730: ago1d_s8_NT_sRNAseq_rep2; Oryza sativa; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11354010">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11354010</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742730</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742730</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456167" alias="GSM5742731_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456167</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742731_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742731: ago1d_s8_NT_sRNAseq_rep3; Oryza sativa; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11354011">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11354011</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742731</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742731</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456168" alias="GSM5742732_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456168</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742732_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742732: wt_s8_LT_sRNAseq_rep1; Oryza sativa; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11354012">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11354012</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742732</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742732</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456169" alias="GSM5742733_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456169</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742733_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742733: wt_s8_LT_sRNAseq_rep2; Oryza sativa; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11354013">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11354013</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742733</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742733</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456170" alias="GSM5742734_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456170</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742734_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742734: wt_s8_LT_sRNAseq_rep3; Oryza sativa; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11354014">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11354014</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742734</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742734</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456171" alias="GSM5742735_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456171</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742735_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742735: wt_s8_NT_sRNAseq_rep1; Oryza sativa; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11354015">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11354015</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742735</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742735</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456172" alias="GSM5742736_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456172</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742736_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742736: wt_s8_NT_sRNAseq_rep2; Oryza sativa; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11354016">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11354016</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742736</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742736</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456173" alias="GSM5742737_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456173</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742737_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742737: wt_s8_NT_sRNAseq_rep3; Oryza sativa; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11354017">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11354017</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742737</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742737</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456174" alias="GSM5742738_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456174</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742738_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742738: ago1d_s9_LT_sRNAseq_rep1; Oryza sativa; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11354018">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11354018</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742738</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742738</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456175" alias="GSM5742739_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456175</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742739_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742739: ago1d_s9_LT_sRNAseq_rep2; Oryza sativa; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11354019">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11354019</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742739</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742739</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456176" alias="GSM5742740_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456176</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742740_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742740: ago1d_s9_LT_sRNAseq_rep3; Oryza sativa; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11354020">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11354020</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742740</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742740</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456177" alias="GSM5742741_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456177</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742741_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742741: ago1d_s9_NT_sRNAseq_rep1; Oryza sativa; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11354021">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11354021</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742741</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742741</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456178" alias="GSM5742742_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456178</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742742_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742742: ago1d_s9_NT_sRNAseq_rep2; Oryza sativa; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11354022">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11354022</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742742</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742742</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456179" alias="GSM5742743_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456179</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742743_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742743: ago1d_s9_NT_sRNAseq_rep3; Oryza sativa; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11354023">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11354023</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742743</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742743</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456180" alias="GSM5742744_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456180</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742744_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742744: wt_s9_LT_sRNAseq_rep1; Oryza sativa; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11354024">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11354024</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742744</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742744</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456181" alias="GSM5742745_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456181</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742745_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742745: wt_s9_LT_sRNAseq_rep2; Oryza sativa; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11354025">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11354025</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742745</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742745</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456182" alias="GSM5742746_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456182</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742746_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742746: wt_s9_LT_sRNAseq_rep3; Oryza sativa; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11354026">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11354026</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742746</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742746</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456183" alias="GSM5742747_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456183</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742747_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742747: wt_s9_NT_sRNAseq_rep1; Oryza sativa; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11354027">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11354027</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742747</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742747</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456184" alias="GSM5742748_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456184</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742748_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742748: wt_s9_NT_sRNAseq_rep2; Oryza sativa; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11354028">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11354028</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742748</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742748</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13456185" alias="GSM5742749_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13456185</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5742749_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5742749: wt_s9_NT_sRNAseq_rep3; Oryza sativa; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP351633">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP351633</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA790833</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11354029">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11354029</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5742749</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5742749</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>All samples were harvested and frozen immediately in liquid nitrogen and total RNA was extracted with TRIzol reagent (Invitrogen) All of the RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq libraries were prepared for sequencing using standard Illumina protocols RNA-seq, small RNA-seq and AGO1d-FLAG RIP-seq</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
