<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX23268088" alias="wild type-1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23268088</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14156959">wild type-1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>WT-1</TITLE>
    <STUDY_REF accession="SRP484341">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP484341</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14156959">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNAs were used for sRNA separation, library construction, and sequencing. The sequencing was performed on an Illumina Hiseq 2500 platform (Lc-Bio Technologies; Hangzhou, China) to obtain 50 bp single end reads</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20169985">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20169985</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|zhzhxiang">wild type-1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>wild type-1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23268089" alias="wild type-2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23268089</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14156959">wild type-2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>WT-2</TITLE>
    <STUDY_REF accession="SRP484341">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP484341</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14156959">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNAs were used for sRNA separation, library construction, and sequencing. The sequencing was performed on an Illumina Hiseq 2500 platform (Lc-Bio Technologies; Hangzhou, China) to obtain 50 bp single end reads</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20169986">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20169986</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|zhzhxiang">wild type-2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>wild type-2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23268090" alias="dcl2b mutant-1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23268090</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14156959">dcl2b mutant-1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>dcl2b-1</TITLE>
    <STUDY_REF accession="SRP484341">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP484341</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14156959">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNAs were used for sRNA separation, library construction, and sequencing. The sequencing was performed on an Illumina Hiseq 2500 platform (Lc-Bio Technologies; Hangzhou, China) to obtain 50 bp single end reads</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20169987">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20169987</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|zhzhxiang">dcl2b mutant-1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>dcl2b mutant-1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23268091" alias="dcl2b mutant-2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23268091</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14156959">dcl2b mutant-2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>dcl2b-2</TITLE>
    <STUDY_REF accession="SRP484341">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP484341</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14156959">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNAs were used for sRNA separation, library construction, and sequencing. The sequencing was performed on an Illumina Hiseq 2500 platform (Lc-Bio Technologies; Hangzhou, China) to obtain 50 bp single end reads</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20169988">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20169988</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|zhzhxiang">dcl2b mutant-2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>dcl2b mutant-2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
