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    <TITLE>CAP222_2020 Multiplexed Illumina MiSeq of HIV: 8 weeks post-infection</TITLE>
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      <PRIMARY_ID>SRX22328101</PRIMARY_ID>
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    <TITLE>CAP222_3120 Multiplexed Illumina MiSeq of HIV: 38 weeks post-infection</TITLE>
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        <PRIMARY_ID>SRP469636</PRIMARY_ID>
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          <PRIMARY_ID>SRS19378156</PRIMARY_ID>
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    <TITLE>CAP244_4370 Multiplexed Illumina MiSeq of HIV: 332 weeks post-infection</TITLE>
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        <PRIMARY_ID>SRP469636</PRIMARY_ID>
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          <PRIMARY_ID>SRS19378161</PRIMARY_ID>
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        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX22328103</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP244_4390_359WPI</SUBMITTER_ID>
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    <TITLE>CAP244_4390 Multiplexed Illumina MiSeq of HIV: 359 weeks post-infection</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS19378157</PRIMARY_ID>
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          <PAIRED/>
        </LIBRARY_LAYOUT>
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        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <PRIMARY_ID>SRX22328104</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP244_4400_372WPI</SUBMITTER_ID>
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    <TITLE>CAP244_4400 Multiplexed Illumina MiSeq of HIV: 372 weeks post-infection</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS19378155</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP244_4400</SUBMITTER_ID>
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          <PAIRED/>
        </LIBRARY_LAYOUT>
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        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX22328105</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP268_2000_008WPI</SUBMITTER_ID>
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    <TITLE>CAP268_2000 Multiplexed Illumina MiSeq of HIV: 8 weeks post-infection</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS19378158</PRIMARY_ID>
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        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX22328106</PRIMARY_ID>
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    <TITLE>CAP268_3100 Multiplexed Illumina MiSeq of HIV: 32 weeks post-infection</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
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      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378160</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP268_3100</SUBMITTER_ID>
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          <PAIRED/>
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        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX22328107</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP222_4190_095WPI</SUBMITTER_ID>
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    <TITLE>CAP222_4190 Multiplexed Illumina MiSeq of HIV: 95 weeks post-infection</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS19378154</PRIMARY_ID>
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      <PRIMARY_ID>SRX22328108</PRIMARY_ID>
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    <TITLE>CAP268_3160 Multiplexed Illumina MiSeq of HIV: 58 weeks post-infection</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
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          <PRIMARY_ID>SRS19378159</PRIMARY_ID>
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      <PRIMARY_ID>SRX22328109</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP268_4180_086WPI</SUBMITTER_ID>
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    <TITLE>CAP268_4180 Multiplexed Illumina MiSeq of HIV: 86 weeks post-infection</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
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          <PRIMARY_ID>SRS19378164</PRIMARY_ID>
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        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX22328110</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP268_4220_137WPI</SUBMITTER_ID>
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    <TITLE>CAP268_4220 Multiplexed Illumina MiSeq of HIV: 137 weeks post-infection</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS19378165</PRIMARY_ID>
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        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
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          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328111</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP268_4240_163WPI</SUBMITTER_ID>
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    <TITLE>CAP268_4240 Multiplexed Illumina MiSeq of HIV: 163 weeks post-infection</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378172</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP268_4240</SUBMITTER_ID>
        </IDENTIFIERS>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP268_4240_163WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
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          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328112</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP268_4260_189WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP268_4260 Multiplexed Illumina MiSeq of HIV: 189 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378162">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378162</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP268_4260</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP268_4260_189WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328113" alias="CAP268_4280_217WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328113</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP268_4280_217WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP268_4280 Multiplexed Illumina MiSeq of HIV: 217 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378163">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378163</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP268_4280</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP268_4280_217WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328114" alias="CAP277_2000_008WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328114</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP277_2000_008WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP277_2000 Multiplexed Illumina MiSeq of HIV: 8 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378184">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378184</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP277_2000</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP277_2000_008WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328115" alias="CAP277_3090_030WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328115</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP277_3090_030WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP277_3090 Multiplexed Illumina MiSeq of HIV: 30 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378183">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378183</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP277_3090</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP277_3090_030WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328116" alias="CAP277_3160_058WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328116</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP277_3160_058WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP277_3160 Multiplexed Illumina MiSeq of HIV: 58 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378166">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378166</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP277_3160</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP277_3160_058WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328117" alias="CAP277_4180_085WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328117</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP277_4180_085WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP277_4180 Multiplexed Illumina MiSeq of HIV: 85 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378167">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378167</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP277_4180</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP277_4180_085WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328118" alias="CAP280_4270_209WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328118</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP280_4270_209WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP280_4270 Multiplexed Illumina MiSeq of HIV: 209 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378170">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378170</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP280_4270</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP280_4270_209WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328119" alias="CAP280_4280_222WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328119</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP280_4280_222WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP280_4280 Multiplexed Illumina MiSeq of HIV: 222 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378168">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378168</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP280_4280</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP280_4280_222WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328120" alias="CAP280_4310_256WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328120</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP280_4310_256WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP280_4310 Multiplexed Illumina MiSeq of HIV: 256 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378191">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378191</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP280_4310</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP280_4310_256WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328121" alias="CAP280_4340_296WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328121</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP280_4340_296WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP280_4340 Multiplexed Illumina MiSeq of HIV: 296 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378169">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378169</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP280_4340</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP280_4340_296WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328122" alias="CAP333_2000_004WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328122</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP333_2000_004WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP333_2000 Multiplexed Illumina MiSeq of HIV: 4 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378171">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378171</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP333_2000</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP333_2000_004WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328123" alias="CAP333_3110_033WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328123</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP333_3110_033WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP333_3110 Multiplexed Illumina MiSeq of HIV: 33 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378173">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378173</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP333_3110</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP333_3110_033WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328124" alias="CAP222_4250_174WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328124</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP222_4250_174WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP222_4250 Multiplexed Illumina MiSeq of HIV: 174 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378176">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378176</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP222_4250</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP222_4250_174WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328125" alias="CAP333_4170_068WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328125</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP333_4170_068WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP333_4170 Multiplexed Illumina MiSeq of HIV: 68 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378174">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378174</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP333_4170</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP333_4170_068WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328126" alias="CAP333_4180_082WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328126</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP333_4180_082WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP333_4180 Multiplexed Illumina MiSeq of HIV: 82 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378178">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378178</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP333_4180</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP333_4180_082WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328127" alias="CAP333_4200_109WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328127</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP333_4200_109WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP333_4200 Multiplexed Illumina MiSeq of HIV: 109 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378175">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378175</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP333_4200</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP333_4200_109WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328128" alias="CAP333_4220_133WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328128</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP333_4220_133WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP333_4220 Multiplexed Illumina MiSeq of HIV: 133 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378177">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378177</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP333_4220</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP333_4220_133WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328129" alias="CAP333_4240_156WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328129</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP333_4240_156WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP333_4240 Multiplexed Illumina MiSeq of HIV: 156 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378181">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378181</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP333_4240</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP333_4240_156WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328130" alias="CAP337_2000_009WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328130</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP337_2000_009WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP337_2000 Multiplexed Illumina MiSeq of HIV: 9 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378182">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378182</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP337_2000</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP337_2000_009WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328131" alias="CAP337_3090_029WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328131</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP337_3090_029WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP337_3090 Multiplexed Illumina MiSeq of HIV: 29 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378179">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378179</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP337_3090</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP337_3090_029WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328132" alias="CAP337_3160_059WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328132</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP337_3160_059WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP337_3160 Multiplexed Illumina MiSeq of HIV: 59 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378180">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378180</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP337_3160</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP337_3160_059WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328133" alias="CAP337_4180_087WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328133</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP337_4180_087WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP337_4180 Multiplexed Illumina MiSeq of HIV: 87 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378186">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378186</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP337_4180</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP337_4180_087WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328134" alias="CAP337_4200_111WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328134</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP337_4200_111WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP337_4200 Multiplexed Illumina MiSeq of HIV: 111 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378185">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378185</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP337_4200</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP337_4200_111WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328135" alias="CAP222_4270_200WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328135</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP222_4270_200WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP222_4270 Multiplexed Illumina MiSeq of HIV: 200 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378188">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378188</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP222_4270</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP222_4270_200WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328136" alias="CAP337_4230_151WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328136</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP337_4230_151WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP337_4230 Multiplexed Illumina MiSeq of HIV: 151 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378192">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378192</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP337_4230</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP337_4230_151WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328137" alias="CAP337_4240_163WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328137</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP337_4240_163WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP337_4240 Multiplexed Illumina MiSeq of HIV: 163 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378187">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378187</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP337_4240</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP337_4240_163WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328138" alias="CAP372_2000_003WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328138</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP372_2000_003WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP372_2000 Multiplexed Illumina MiSeq of HIV: 3 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378189">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378189</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP372_2000</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP372_2000_003WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328139" alias="CAP372_3100_027WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328139</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP372_3100_027WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP372_3100 Multiplexed Illumina MiSeq of HIV: 27 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378190">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378190</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP372_3100</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP372_3100_027WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328140" alias="CAP372_3160_053WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328140</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP372_3160_053WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP372_3160 Multiplexed Illumina MiSeq of HIV: 53 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378195">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378195</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP372_3160</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP372_3160_053WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328141" alias="CAP372_4180_081WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328141</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP372_4180_081WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP372_4180 Multiplexed Illumina MiSeq of HIV: 81 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378196">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378196</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP372_4180</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP372_4180_081WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328142" alias="CAP372_4200_106WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328142</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP372_4200_106WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP372_4200 Multiplexed Illumina MiSeq of HIV: 106 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378193">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378193</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP372_4200</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP372_4200_106WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328143" alias="CAP372_4220_132WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328143</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP372_4220_132WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP372_4220 Multiplexed Illumina MiSeq of HIV: 132 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378197">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378197</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP372_4220</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP372_4220_132WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328144" alias="CAP372_4240_161WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328144</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP372_4240_161WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP372_4240 Multiplexed Illumina MiSeq of HIV: 161 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378194">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378194</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP372_4240</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP372_4240_161WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328145" alias="CAP372_4250_172WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328145</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP372_4250_172WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP372_4250 Multiplexed Illumina MiSeq of HIV: 172 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378198">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378198</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP372_4250</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP372_4250_172WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328146" alias="CAP222_4290_224WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328146</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP222_4290_224WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP222_4290 Multiplexed Illumina MiSeq of HIV: 224 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378199">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378199</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP222_4290</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP222_4290_224WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328147" alias="CAP372_9999_182WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328147</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP372_9999_182WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP372_9999 Multiplexed Illumina MiSeq of HIV: 182 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378200">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378200</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP372_9999</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP372_9999_182WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328148" alias="CAP380_2000_008WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328148</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP380_2000_008WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP380_2000 Multiplexed Illumina MiSeq of HIV: 8 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378203">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378203</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP380_2000</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP380_2000_008WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328149" alias="CAP380_3110_037WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328149</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP380_3110_037WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP380_3110 Multiplexed Illumina MiSeq of HIV: 37 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378201">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378201</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP380_3110</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP380_3110_037WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328150" alias="CAP222_4330_278WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328150</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP222_4330_278WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP222_4330 Multiplexed Illumina MiSeq of HIV: 278 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378202">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378202</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP222_4330</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP222_4330_278WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328151" alias="CAP222_4350_304WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328151</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP222_4350_304WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP222_4350 Multiplexed Illumina MiSeq of HIV: 304 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378204">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378204</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP222_4350</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP222_4350_304WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328152" alias="CAP222_4360_313WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328152</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP222_4360_313WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP222_4360 Multiplexed Illumina MiSeq of HIV: 313 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378205">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378205</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP222_4360</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP222_4360_313WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328153" alias="CAP244_2000_009WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328153</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP244_2000_009WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP244_2000 Multiplexed Illumina MiSeq of HIV: 9 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378212">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378212</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP244_2000</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP244_2000_009WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328154" alias="CAP244_3100_033WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328154</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP244_3100_033WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP244_3100 Multiplexed Illumina MiSeq of HIV: 33 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378206">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378206</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP244_3100</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP244_3100_033WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328155" alias="CAP244_3160_056WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328155</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP244_3160_056WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP244_3160 Multiplexed Illumina MiSeq of HIV: 56 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378214">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378214</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP244_3160</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP244_3160_056WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328156" alias="CAP244_4180_081WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328156</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP244_4180_081WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP244_4180 Multiplexed Illumina MiSeq of HIV: 81 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378208">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378208</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP244_4180</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP244_4180_081WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328157" alias="CAP244_4200_107WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328157</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP244_4200_107WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP244_4200 Multiplexed Illumina MiSeq of HIV: 107 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378209">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378209</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP244_4200</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP244_4200_107WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328158" alias="CAP244_4220_137WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328158</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP244_4220_137WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP244_4220 Multiplexed Illumina MiSeq of HIV: 137 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378213">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378213</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP244_4220</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP244_4220_137WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328159" alias="CAP244_4230_150WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328159</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP244_4230_150WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP244_4230 Multiplexed Illumina MiSeq of HIV: 150 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378207">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378207</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP244_4230</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP244_4230_150WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328160" alias="CAP222_4170_070WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328160</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP222_4170_070WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP222_4170 Multiplexed Illumina MiSeq of HIV: 70 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378211">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378211</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP222_4170</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP222_4170_070WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328161" alias="CAP244_4260_191WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328161</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP244_4260_191WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP244_4260 Multiplexed Illumina MiSeq of HIV: 191 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378210">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378210</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP244_4260</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP244_4260_191WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328162" alias="CAP244_4290_230WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328162</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP244_4290_230WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP244_4290 Multiplexed Illumina MiSeq of HIV: 230 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378216">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378216</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP244_4290</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP244_4290_230WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328163" alias="CAP244_4310_255WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328163</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP244_4310_255WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP244_4310 Multiplexed Illumina MiSeq of HIV: 255 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378215">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378215</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP244_4310</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP244_4310_255WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328164" alias="CAP244_4330_282WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328164</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP244_4330_282WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP244_4330 Multiplexed Illumina MiSeq of HIV: 282 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378223">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378223</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP244_4330</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP244_4330_282WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328165" alias="CAP244_4350_307WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328165</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP244_4350_307WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP244_4350 Multiplexed Illumina MiSeq of HIV: 307 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378221">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378221</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP244_4350</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP244_4350_307WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328166" alias="CAP380_3160_059WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328166</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP380_3160_059WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP380_3160 Multiplexed Illumina MiSeq of HIV: 59 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378217">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378217</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP380_3160</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP380_3160_059WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328167" alias="CAP380_4180_085WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328167</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP380_4180_085WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP380_4180 Multiplexed Illumina MiSeq of HIV: 85 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378220">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378220</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP380_4180</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP380_4180_085WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328168" alias="CAP380_4200_110WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328168</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP380_4200_110WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP380_4200 Multiplexed Illumina MiSeq of HIV: 110 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378222">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378222</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP380_4200</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP380_4200_110WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328169" alias="CAP380_4210_125WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328169</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP380_4210_125WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP380_4210 Multiplexed Illumina MiSeq of HIV: 125 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378219">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378219</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP380_4210</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP380_4210_125WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328170" alias="CAP217_4180_087WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328170</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP217_4180_087WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP217_4180 Multiplexed Illumina MiSeq of HIV: 87 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378218">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378218</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP217_4180</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP217_4180_087WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328171" alias="CAP316_2000_012WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328171</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP316_2000_012WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP316_2000 Multiplexed Illumina MiSeq of HIV: 12 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378224">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378224</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP316_2000</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP316_2000_012WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328172" alias="CAP316_3100_036WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328172</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP316_3100_036WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP316_3100 Multiplexed Illumina MiSeq of HIV: 36 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378226">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378226</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP316_3100</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP316_3100_036WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328173" alias="CAP222_4310_251WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328173</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP222_4310_251WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP222_4310 Multiplexed Illumina MiSeq of HIV: 251 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378227">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378227</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP222_4310</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP222_4310_251WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328174" alias="CAP316_3140_053WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328174</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP316_3140_053WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP316_3140 Multiplexed Illumina MiSeq of HIV: 53 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378225">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378225</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP316_3140</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP316_3140_053WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328175" alias="CAP316_4180_090WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328175</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP316_4180_090WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP316_4180 Multiplexed Illumina MiSeq of HIV: 90 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378232">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378232</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP316_4180</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP316_4180_090WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328176" alias="CAP316_4200_114WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328176</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP316_4200_114WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP316_4200 Multiplexed Illumina MiSeq of HIV: 114 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378228">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378228</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP316_4200</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP316_4200_114WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328177" alias="CAP316_4220_141WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328177</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP316_4220_141WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP316_4220 Multiplexed Illumina MiSeq of HIV: 141 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378230">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378230</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP316_4220</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP316_4220_141WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328178" alias="CAP316_4240_166WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328178</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP316_4240_166WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP316_4240 Multiplexed Illumina MiSeq of HIV: 166 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378229">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378229</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP316_4240</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP316_4240_166WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328179" alias="CAP316_4260_192WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328179</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP316_4260_192WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP316_4260 Multiplexed Illumina MiSeq of HIV: 192 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378233">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378233</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP316_4260</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP316_4260_192WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328180" alias="CAP316_4270_205WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328180</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP316_4270_205WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP316_4270 Multiplexed Illumina MiSeq of HIV: 205 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378235">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378235</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP316_4270</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP316_4270_205WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328181" alias="CAP222_4210_122WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328181</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP222_4210_122WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP222_4210 Multiplexed Illumina MiSeq of HIV: 122 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378234">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378234</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP222_4210</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP222_4210_122WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328182" alias="CAP277_4200_110WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328182</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP277_4200_110WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP277_4200 Multiplexed Illumina MiSeq of HIV: 110 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378231">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378231</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP277_4200</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP277_4200_110WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328183" alias="CAP277_4220_137WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328183</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP277_4220_137WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP277_4220 Multiplexed Illumina MiSeq of HIV: 137 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378237">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378237</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP277_4220</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP277_4220_137WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328184" alias="CAP277_4240_163WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328184</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP277_4240_163WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP277_4240 Multiplexed Illumina MiSeq of HIV: 163 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378236">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378236</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP277_4240</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP277_4240_163WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328185" alias="CAP277_4260_189WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328185</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP277_4260_189WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP277_4260 Multiplexed Illumina MiSeq of HIV: 189 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378241">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378241</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP277_4260</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP277_4260_189WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328186" alias="CAP277_4280_215WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328186</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP277_4280_215WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP277_4280 Multiplexed Illumina MiSeq of HIV: 215 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378242">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378242</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP277_4280</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP277_4280_215WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328187" alias="CAP277_4300_243WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328187</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP277_4300_243WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP277_4300 Multiplexed Illumina MiSeq of HIV: 243 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378238">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378238</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP277_4300</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP277_4300_243WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328188" alias="CAP277_4310_254WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328188</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP277_4310_254WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP277_4310 Multiplexed Illumina MiSeq of HIV: 254 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378239">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378239</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP277_4310</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP277_4310_254WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328189" alias="CAP280_2000_012WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328189</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP280_2000_012WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP280_2000 Multiplexed Illumina MiSeq of HIV: 12 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378243">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378243</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP280_2000</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP280_2000_012WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328190" alias="CAP280_3100_036WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328190</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP280_3100_036WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP280_3100 Multiplexed Illumina MiSeq of HIV: 36 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378240">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378240</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP280_3100</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP280_3100_036WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328191" alias="CAP280_3160_063WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328191</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP280_3160_063WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP280_3160 Multiplexed Illumina MiSeq of HIV: 63 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378244">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378244</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP280_3160</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP280_3160_063WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328192" alias="CAP222_4230_148WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328192</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP222_4230_148WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP222_4230 Multiplexed Illumina MiSeq of HIV: 148 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378245">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378245</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP222_4230</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP222_4230_148WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328193" alias="CAP280_4180_090WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328193</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP280_4180_090WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP280_4180 Multiplexed Illumina MiSeq of HIV: 90 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378247">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378247</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP280_4180</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP280_4180_090WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328194" alias="CAP280_4200_117WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328194</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP280_4200_117WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP280_4200 Multiplexed Illumina MiSeq of HIV: 117 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378248">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378248</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP280_4200</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP280_4200_117WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328195" alias="CAP280_4230_156WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328195</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP280_4230_156WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP280_4230 Multiplexed Illumina MiSeq of HIV: 156 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378246">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378246</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP280_4230</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP280_4230_156WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22328196" alias="CAP280_4250_184WPI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22328196</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13903934">CAP280_4250_184WPI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>CAP280_4250 Multiplexed Illumina MiSeq of HIV: 184 weeks post-infection</TITLE>
    <STUDY_REF accession="SRP469636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP469636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13903934">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Viral RNA was reverse transcribed to cDNA using Superscript IV Reverse Transcriptase (Invitrogen). Multiple cDNA primers (with PrimerIDs) were multiplexed to generate cDNA templates corresponding to multiple regions of the genome. A first round PCR was performed using the KAPA2G Fast Multiplex Mix (Kapa Biosystems), followed by a second round PCR using the Expand High Fidelity PCR System (Roche) to incorporate Illumina MiSeq version 3 indexes and adapters. PCR products were purified using AMPureXP beads (Beckman Coulter).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19378249">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19378249</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|lynn.tyers@orcid">CAP280_4250</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CAP280_4250_184WPI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
