<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX18382556" alias="LB_contorta">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18382556</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12302570">LB_contorta</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Ten cells whole transcriptome amplication of  raw reads of Brachonella contorta</TITLE>
    <STUDY_REF accession="SRP409911">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409911</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12302570">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Library was constructed from the cDNA extracted from one hand-picked, starved, and washed cell of Brachonella contorta ciliates. Single cell transcriptome was generated with SMART-Seq v4 kit and the cDNA library was sequenced using Illumina Novaseq 150-bp paired-end reads in Beijing Novozhiyuan Technology Co., Ltd.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS15868195">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15868195</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leejia3547@gmail.com">LBC</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>LB_contorta</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC SINGLE CELL</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18382557" alias="LM_major">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18382557</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12302570">LM_major</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq raw reads of Metopus major</TITLE>
    <STUDY_REF accession="SRP409911">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409911</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12302570">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Library was constructed from the RNA extracted from 1400 mL of mass-culture of Metopus major ciliates.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS15868196">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15868196</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leejia3547@gmail.com">LM2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>LM_major</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18382558" alias="LM_paraes">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18382558</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12302570">LM_paraes</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq raw reads of Metopus paraes</TITLE>
    <STUDY_REF accession="SRP409911">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409911</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12302570">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Library was constructed from the RNA extracted from 1400 mL of mass-culture of Metopus paraes ciliates.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS15868197">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15868197</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leejia3547@gmail.com">LMP</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>LM_paraes</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18382559" alias="LN_sp">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18382559</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12302570">LN_sp</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Twelve cells whole transcriptome amplication of raw reads of Nyctotheroides sp.</TITLE>
    <STUDY_REF accession="SRP409911">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409911</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12302570">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Library was constructed from the cDNA extracted from one hand-picked, starved, and washed cell of Nyctotheroides sp. ciliates. Single cell transcriptome was generated with SMART-Seq v4 kit and the cDNA library was sequenced using Illumina Novaseq 150-bp paired-end reads in Beijing Novozhiyuan Technology Co., Ltd.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS15868198">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15868198</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leejia3547@gmail.com">LNS</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>LN_sp</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC SINGLE CELL</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18382560" alias="LSul_cf_uniserialis">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18382560</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12302570">LSul_cf_uniserialis</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Single cell whole transcriptome amplication of raw reads of Sulfonecta cf. uniserialis</TITLE>
    <STUDY_REF accession="SRP409911">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409911</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12302570">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Library was constructed from the cDNA extracted from one hand-picked, starved, and washed cell of Sulfonecta cf. uniserialis ciliates. Single cell transcriptome was generated with SMART-Seq v4 kit and the cDNA library was sequenced using Illumina Novaseq 150-bp paired-end reads in Beijing Novozhiyuan Technology Co., Ltd.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS15868199">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15868199</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leejia3547@gmail.com">LSul</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>LSul_cf_uniserialis</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC SINGLE CELL</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
