<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX18383594" alias="01,02,03,04">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18383594</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12328785">01,02,03,04</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of human Peripheral blood: Adult peripheral T cells</TITLE>
    <STUDY_REF accession="SRP409930">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409930</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12328785">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from cells using the RNeasy Mini Plus Kit, followed by fragmented into small pieces with fragment buffer at appropriate temperature. The RNA library was constructed by MGIEasy RNA Directional Library Preparation Kit prior to standard quality control for sequencing via the BGIseq500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS15869229">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15869229</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lwl1027">D465_1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>01,02,03,04</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <BGISEQ>
        <INSTRUMENT_MODEL>BGISEQ-500</INSTRUMENT_MODEL>
      </BGISEQ>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18383595" alias="01,02">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18383595</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12328785">01,02</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of human Peripheral blood: Adult peripheral T cells</TITLE>
    <STUDY_REF accession="SRP409930">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409930</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12328785">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from cells using the RNeasy Mini Plus Kit, followed by fragmented into small pieces with fragment buffer at appropriate temperature. The RNA library was constructed by MGIEasy RNA Directional Library Preparation Kit prior to standard quality control for sequencing via the BGIseq500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS15869228">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15869228</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lwl1027">D465_2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>01,02</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <BGISEQ>
        <INSTRUMENT_MODEL>BGISEQ-500</INSTRUMENT_MODEL>
      </BGISEQ>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18383596" alias="0304">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18383596</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12328785">0304</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of human Peripheral blood: Adult peripheral T cells</TITLE>
    <STUDY_REF accession="SRP409930">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409930</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12328785">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from cells using the RNeasy Mini Plus Kit, followed by fragmented into small pieces with fragment buffer at appropriate temperature. The RNA library was constructed by MGIEasy RNA Directional Library Preparation Kit prior to standard quality control for sequencing via the BGIseq500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS15869230">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15869230</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lwl1027">D468_4</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>0304</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <BGISEQ>
        <INSTRUMENT_MODEL>BGISEQ-500</INSTRUMENT_MODEL>
      </BGISEQ>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18383597" alias="15,16">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18383597</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12328785">15,16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of human Peripheral blood: Adult peripheral T cells</TITLE>
    <STUDY_REF accession="SRP409930">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409930</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12328785">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from cells using the RNeasy Mini Plus Kit, followed by fragmented into small pieces with fragment buffer at appropriate temperature. The RNA library was constructed by MGIEasy RNA Directional Library Preparation Kit prior to standard quality control for sequencing via the BGIseq500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS15869231">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15869231</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lwl1027">D468_5</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15,16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <BGISEQ>
        <INSTRUMENT_MODEL>BGISEQ-500</INSTRUMENT_MODEL>
      </BGISEQ>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18383598" alias="97,98">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18383598</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12328785">97,98</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of human Peripheral blood: Adult peripheral T cells</TITLE>
    <STUDY_REF accession="SRP409930">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409930</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12328785">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from cells using the RNeasy Mini Plus Kit, followed by fragmented into small pieces with fragment buffer at appropriate temperature. The RNA library was constructed by MGIEasy RNA Directional Library Preparation Kit prior to standard quality control for sequencing via the BGIseq500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS15869232">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15869232</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lwl1027">D468_8</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>97,98</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <BGISEQ>
        <INSTRUMENT_MODEL>BGISEQ-500</INSTRUMENT_MODEL>
      </BGISEQ>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18383599" alias="101,102">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18383599</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12328785">101,102</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of human Peripheral blood: Adult peripheral T cells</TITLE>
    <STUDY_REF accession="SRP409930">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409930</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12328785">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from cells using the RNeasy Mini Plus Kit, followed by fragmented into small pieces with fragment buffer at appropriate temperature. The RNA library was constructed by MGIEasy RNA Directional Library Preparation Kit prior to standard quality control for sequencing via the BGIseq500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS15869233">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15869233</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lwl1027">D468_10</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>101,102</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <BGISEQ>
        <INSTRUMENT_MODEL>BGISEQ-500</INSTRUMENT_MODEL>
      </BGISEQ>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18383600" alias="99,100">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18383600</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12328785">99,100</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of human Peripheral blood: Adult peripheral T cells</TITLE>
    <STUDY_REF accession="SRP409930">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409930</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12328785">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from cells using the RNeasy Mini Plus Kit, followed by fragmented into small pieces with fragment buffer at appropriate temperature. The RNA library was constructed by MGIEasy RNA Directional Library Preparation Kit prior to standard quality control for sequencing via the BGIseq500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS15869235">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15869235</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lwl1027">D465_3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>99,100</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <BGISEQ>
        <INSTRUMENT_MODEL>BGISEQ-500</INSTRUMENT_MODEL>
      </BGISEQ>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18383601" alias="03,04">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18383601</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12328785">03,04</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of human Peripheral blood: Adult peripheral T cells</TITLE>
    <STUDY_REF accession="SRP409930">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409930</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12328785">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from cells using the RNeasy Mini Plus Kit, followed by fragmented into small pieces with fragment buffer at appropriate temperature. The RNA library was constructed by MGIEasy RNA Directional Library Preparation Kit prior to standard quality control for sequencing via the BGIseq500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS15869234">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15869234</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lwl1027">D465_4</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>03,04</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <BGISEQ>
        <INSTRUMENT_MODEL>BGISEQ-500</INSTRUMENT_MODEL>
      </BGISEQ>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18383602" alias="13,14">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18383602</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12328785">13,14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of human Peripheral blood: Adult peripheral T cells</TITLE>
    <STUDY_REF accession="SRP409930">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409930</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12328785">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from cells using the RNeasy Mini Plus Kit, followed by fragmented into small pieces with fragment buffer at appropriate temperature. The RNA library was constructed by MGIEasy RNA Directional Library Preparation Kit prior to standard quality control for sequencing via the BGIseq500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS15869236">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15869236</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lwl1027">D465_5</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13,14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <BGISEQ>
        <INSTRUMENT_MODEL>BGISEQ-500</INSTRUMENT_MODEL>
      </BGISEQ>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18383603" alias="13141516">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18383603</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12328785">13141516</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of human Peripheral blood: Adult peripheral T cells</TITLE>
    <STUDY_REF accession="SRP409930">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409930</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12328785">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from cells using the RNeasy Mini Plus Kit, followed by fragmented into small pieces with fragment buffer at appropriate temperature. The RNA library was constructed by MGIEasy RNA Directional Library Preparation Kit prior to standard quality control for sequencing via the BGIseq500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS15869237">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15869237</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lwl1027">D465_8</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13141516</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <BGISEQ>
        <INSTRUMENT_MODEL>BGISEQ-500</INSTRUMENT_MODEL>
      </BGISEQ>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18383604" alias="99100">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18383604</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12328785">99100</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of human Peripheral blood: Adult peripheral T cells</TITLE>
    <STUDY_REF accession="SRP409930">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409930</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12328785">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from cells using the RNeasy Mini Plus Kit, followed by fragmented into small pieces with fragment buffer at appropriate temperature. The RNA library was constructed by MGIEasy RNA Directional Library Preparation Kit prior to standard quality control for sequencing via the BGIseq500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS15869238">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15869238</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lwl1027">D465_10</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>99100</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <BGISEQ>
        <INSTRUMENT_MODEL>BGISEQ-500</INSTRUMENT_MODEL>
      </BGISEQ>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18383605" alias="101102">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18383605</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12328785">101102</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of human Peripheral blood: Adult peripheral T cells</TITLE>
    <STUDY_REF accession="SRP409930">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409930</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12328785">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from cells using the RNeasy Mini Plus Kit, followed by fragmented into small pieces with fragment buffer at appropriate temperature. The RNA library was constructed by MGIEasy RNA Directional Library Preparation Kit prior to standard quality control for sequencing via the BGIseq500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS15869240">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15869240</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lwl1027">D468_1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>101102</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <BGISEQ>
        <INSTRUMENT_MODEL>BGISEQ-500</INSTRUMENT_MODEL>
      </BGISEQ>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18383606" alias="103104">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18383606</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12328785">103104</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of human Peripheral blood: Adult peripheral T cells</TITLE>
    <STUDY_REF accession="SRP409930">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409930</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12328785">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from cells using the RNeasy Mini Plus Kit, followed by fragmented into small pieces with fragment buffer at appropriate temperature. The RNA library was constructed by MGIEasy RNA Directional Library Preparation Kit prior to standard quality control for sequencing via the BGIseq500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS15869239">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15869239</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lwl1027">D468_2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>103104</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <BGISEQ>
        <INSTRUMENT_MODEL>BGISEQ-500</INSTRUMENT_MODEL>
      </BGISEQ>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18383607" alias="0102">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18383607</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12328785">0102</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of human Peripheral blood: Adult peripheral T cells</TITLE>
    <STUDY_REF accession="SRP409930">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409930</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12328785">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from cells using the RNeasy Mini Plus Kit, followed by fragmented into small pieces with fragment buffer at appropriate temperature. The RNA library was constructed by MGIEasy RNA Directional Library Preparation Kit prior to standard quality control for sequencing via the BGIseq500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS15869241">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15869241</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lwl1027">D468_3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>0102</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <BGISEQ>
        <INSTRUMENT_MODEL>BGISEQ-500</INSTRUMENT_MODEL>
      </BGISEQ>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
