<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX23845534" alias="UCSF_VRP_mNGS_031_0697">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845534</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_031_0697</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20665960">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20665960</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267554</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_031_0697</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845535" alias="UCSF_VRP_mNGS_031_0698">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845535</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_031_0698</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20665961">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20665961</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267555</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_031_0698</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845536" alias="UCSF_VRP_mNGS_031_0699">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845536</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_031_0699</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20665962">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20665962</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267556</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_031_0699</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845537" alias="UCSF_VRP_mNGS_031_0700">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845537</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_031_0700</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20665963">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20665963</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267557</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_031_0700</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845538" alias="UCSF_VRP_mNGS_001_0008">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845538</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_001_0008</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20665964">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20665964</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266865</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_001_0008</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845539" alias="UCSF_VRP_mNGS_003_0071">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845539</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_003_0071</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20665965">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20665965</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266928</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_003_0071</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845540" alias="UCSF_VRP_mNGS_031_0701">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845540</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_031_0701</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20665966">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20665966</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267558</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_031_0701</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845541" alias="UCSF_VRP_mNGS_031_0702">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845541</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_031_0702</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20665967">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20665967</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267559</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_031_0702</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845542" alias="UCSF_VRP_mNGS_031_0703">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845542</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_031_0703</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20665968">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20665968</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267560</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_031_0703</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845543" alias="UCSF_VRP_mNGS_034_0770">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845543</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_034_0770</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20665969">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20665969</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267627</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_034_0770</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845544" alias="UCSF_VRP_mNGS_003_0078">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845544</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_003_0078</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20665970">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20665970</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266935</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_003_0078</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845545" alias="UCSF_VRP_mNGS_034_0771">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845545</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_034_0771</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20665971">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20665971</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267628</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_034_0771</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845546" alias="UCSF_VRP_mNGS_034_0772">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845546</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_034_0772</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20665972">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20665972</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267629</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_034_0772</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845547" alias="UCSF_VRP_mNGS_034_0773">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845547</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_034_0773</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20665973">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20665973</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267630</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_034_0773</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845548" alias="UCSF_VRP_mNGS_034_0774">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845548</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_034_0774</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20665974">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20665974</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267631</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_034_0774</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845549" alias="UCSF_VRP_mNGS_034_0775">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845549</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_034_0775</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20665975">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20665975</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267632</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_034_0775</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845550" alias="UCSF_VRP_mNGS_034_0776">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845550</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_034_0776</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20665976">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20665976</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267633</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_034_0776</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845551" alias="UCSF_VRP_mNGS_034_0777">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845551</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_034_0777</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20665977">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20665977</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267634</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_034_0777</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845552" alias="UCSF_VRP_mNGS_034_0778">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845552</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_034_0778</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20665978">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20665978</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267635</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_034_0778</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845553" alias="UCSF_VRP_mNGS_034_0779">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845553</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_034_0779</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20665979">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20665979</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267636</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_034_0779</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845554" alias="UCSF_VRP_mNGS_034_0780">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845554</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_034_0780</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20665980">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20665980</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267637</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_034_0780</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845555" alias="UCSF_VRP_mNGS_003_0079">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845555</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_003_0079</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20665981">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20665981</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266936</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_003_0079</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845556" alias="UCSF_VRP_mNGS_034_0781">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845556</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_034_0781</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20665982">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20665982</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267638</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_034_0781</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845557" alias="UCSF_VRP_mNGS_034_0782">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845557</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_034_0782</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20665983">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20665983</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267639</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_034_0782</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845558" alias="UCSF_VRP_mNGS_034_0783">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845558</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_034_0783</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20665984">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20665984</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267640</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_034_0783</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845559" alias="UCSF_VRP_mNGS_034_0784">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845559</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_034_0784</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20665985">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20665985</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267641</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_034_0784</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845560" alias="UCSF_VRP_mNGS_035_0785">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845560</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_035_0785</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20665986">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20665986</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267642</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_035_0785</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845561" alias="UCSF_VRP_mNGS_035_0786">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845561</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_035_0786</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20665987">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20665987</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267643</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_035_0786</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845562" alias="UCSF_VRP_mNGS_035_0787">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845562</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_035_0787</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20665989">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20665989</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267644</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_035_0787</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845563" alias="UCSF_VRP_mNGS_035_0788">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845563</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_035_0788</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20665988">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20665988</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267645</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_035_0788</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845564" alias="UCSF_VRP_mNGS_035_0789">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845564</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_035_0789</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20665990">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20665990</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267646</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_035_0789</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845565" alias="UCSF_VRP_mNGS_035_0790">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845565</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_035_0790</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20665991">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20665991</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267647</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_035_0790</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845566" alias="UCSF_VRP_mNGS_003_0080">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845566</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_003_0080</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20665992">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20665992</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266937</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_003_0080</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845567" alias="UCSF_VRP_mNGS_036_0834">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845567</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_036_0834</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20665993">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20665993</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267691</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_036_0834</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845568" alias="UCSF_VRP_mNGS_036_0835">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845568</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_036_0835</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20665994">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20665994</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267692</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_036_0835</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845569" alias="UCSF_VRP_mNGS_037_0836">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845569</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_037_0836</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20665995">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20665995</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267693</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_037_0836</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845570" alias="UCSF_VRP_mNGS_037_0837">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845570</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_037_0837</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20665996">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20665996</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267694</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_037_0837</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845571" alias="UCSF_VRP_mNGS_037_0838">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845571</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_037_0838</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20665997">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20665997</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267695</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_037_0838</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845572" alias="UCSF_VRP_mNGS_037_0839">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845572</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_037_0839</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20665999">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20665999</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267696</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_037_0839</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845573" alias="UCSF_VRP_mNGS_037_0840">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845573</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_037_0840</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20665998">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20665998</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267697</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_037_0840</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845574" alias="UCSF_VRP_mNGS_003_0085">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845574</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_003_0085</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666000">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666000</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266942</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_003_0085</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845575" alias="UCSF_VRP_mNGS_037_0841">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845575</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_037_0841</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666001">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666001</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267698</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_037_0841</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845576" alias="UCSF_VRP_mNGS_037_0842">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845576</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_037_0842</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666002">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666002</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267699</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_037_0842</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845577" alias="UCSF_VRP_mNGS_037_0843">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845577</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_037_0843</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666003">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666003</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267700</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_037_0843</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845578" alias="UCSF_VRP_mNGS_037_0844">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845578</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_037_0844</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666004">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666004</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267701</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_037_0844</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845579" alias="UCSF_VRP_mNGS_037_0845">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845579</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_037_0845</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666005">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666005</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267702</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_037_0845</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845580" alias="UCSF_VRP_mNGS_037_0846">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845580</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_037_0846</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666006">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666006</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267703</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_037_0846</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845581" alias="UCSF_VRP_mNGS_037_0847">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845581</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_037_0847</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666007">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666007</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267704</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_037_0847</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845582" alias="UCSF_VRP_mNGS_037_0848">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845582</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_037_0848</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666008">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666008</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267705</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_037_0848</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845583" alias="UCSF_VRP_mNGS_037_0849">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845583</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_037_0849</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666009">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666009</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267706</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_037_0849</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845584" alias="UCSF_VRP_mNGS_037_0850">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845584</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_037_0850</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666010">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666010</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267707</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_037_0850</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845585" alias="UCSF_VRP_mNGS_003_0086">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845585</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_003_0086</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666011">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666011</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266943</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_003_0086</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845586" alias="UCSF_VRP_mNGS_037_0851">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845586</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_037_0851</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666012">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666012</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267708</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_037_0851</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845587" alias="UCSF_VRP_mNGS_037_0852">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845587</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_037_0852</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666013">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666013</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267709</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_037_0852</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845588" alias="UCSF_VRP_mNGS_037_0853">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845588</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_037_0853</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666014">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666014</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267710</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_037_0853</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845589" alias="UCSF_VRP_mNGS_037_0854">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845589</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_037_0854</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666015">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666015</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267711</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_037_0854</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845590" alias="UCSF_VRP_mNGS_037_0855">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845590</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_037_0855</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666016">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666016</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267712</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_037_0855</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845591" alias="UCSF_VRP_mNGS_040_0900">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845591</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_040_0900</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666017">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666017</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267757</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_040_0900</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845592" alias="UCSF_VRP_mNGS_001_0010">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845592</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_001_0010</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666018">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666018</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266867</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_001_0010</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845593" alias="UCSF_VRP_mNGS_004_0091">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845593</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_004_0091</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666019">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666019</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266948</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_004_0091</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845594" alias="UCSF_VRP_mNGS_040_0901">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845594</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_040_0901</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666020">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666020</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267758</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_040_0901</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845595" alias="UCSF_VRP_mNGS_040_0902">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845595</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_040_0902</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666021">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666021</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267759</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_040_0902</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845596" alias="UCSF_VRP_mNGS_040_0903">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845596</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_040_0903</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666022">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666022</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267760</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_040_0903</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845597" alias="UCSF_VRP_mNGS_040_0904">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845597</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_040_0904</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666023">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666023</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267761</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_040_0904</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845598" alias="UCSF_VRP_mNGS_040_0905">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845598</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_040_0905</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666024">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666024</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267762</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_040_0905</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845599" alias="UCSF_VRP_mNGS_040_0906">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845599</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_040_0906</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666025">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666025</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267763</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_040_0906</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845600" alias="UCSF_VRP_mNGS_040_0907">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845600</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_040_0907</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666026">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666026</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267764</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_040_0907</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845601" alias="UCSF_VRP_mNGS_040_0908">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845601</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_040_0908</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666027">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666027</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267765</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_040_0908</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845602" alias="UCSF_VRP_mNGS_040_0909">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845602</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_040_0909</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666028">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666028</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267766</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_040_0909</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845603" alias="UCSF_VRP_mNGS_040_0910">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845603</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_040_0910</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666029">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666029</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267767</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_040_0910</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845604" alias="UCSF_VRP_mNGS_004_0092">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845604</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_004_0092</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666030">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666030</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266949</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_004_0092</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845605" alias="UCSF_VRP_mNGS_040_0911">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845605</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_040_0911</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666031">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666031</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267768</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_040_0911</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845606" alias="UCSF_VRP_mNGS_040_0912">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845606</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_040_0912</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666032">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666032</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267769</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_040_0912</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845607" alias="UCSF_VRP_mNGS_040_0913">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845607</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_040_0913</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666033">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666033</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267770</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_040_0913</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845608" alias="UCSF_VRP_mNGS_041_0914">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845608</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_041_0914</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666034">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666034</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267771</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_041_0914</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845609" alias="UCSF_VRP_mNGS_041_0915">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845609</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_041_0915</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666035">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666035</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267772</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_041_0915</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845610" alias="UCSF_VRP_mNGS_041_0916">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845610</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_041_0916</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666036">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666036</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267773</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_041_0916</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845611" alias="UCSF_VRP_mNGS_041_0917">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845611</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_041_0917</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666037">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666037</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267774</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_041_0917</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845612" alias="UCSF_VRP_mNGS_041_0918">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845612</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_041_0918</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666038">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666038</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267775</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_041_0918</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845613" alias="UCSF_VRP_mNGS_041_0919">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845613</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_041_0919</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666039">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666039</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267776</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_041_0919</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845614" alias="UCSF_VRP_mNGS_041_0920">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845614</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_041_0920</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666040">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666040</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267777</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_041_0920</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845615" alias="UCSF_VRP_mNGS_043_0964">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845615</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_043_0964</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666041">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666041</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267821</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_043_0964</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845616" alias="UCSF_VRP_mNGS_043_0965">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845616</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_043_0965</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666042">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666042</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267822</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_043_0965</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845617" alias="UCSF_VRP_mNGS_043_0966">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845617</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_043_0966</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666043">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666043</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267823</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_043_0966</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845618" alias="UCSF_VRP_mNGS_043_0967">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845618</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_043_0967</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666044">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666044</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267824</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_043_0967</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845619" alias="UCSF_VRP_mNGS_043_0968">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845619</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_043_0968</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666045">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666045</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267825</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_043_0968</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845620" alias="UCSF_VRP_mNGS_043_0969">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845620</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_043_0969</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666046">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666046</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267826</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_043_0969</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845621" alias="UCSF_VRP_mNGS_043_0970">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845621</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_043_0970</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666047">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666047</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267827</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_043_0970</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845622" alias="UCSF_VRP_mNGS_004_0098">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845622</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_004_0098</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666048">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666048</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266955</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_004_0098</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845623" alias="UCSF_VRP_mNGS_043_0971">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845623</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_043_0971</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666049">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666049</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267828</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_043_0971</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845624" alias="UCSF_VRP_mNGS_043_0972">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845624</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_043_0972</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666050">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666050</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267829</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_043_0972</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845625" alias="UCSF_VRP_mNGS_043_0973">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845625</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_043_0973</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666051">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666051</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267830</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_043_0973</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845626" alias="UCSF_VRP_mNGS_043_0974">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845626</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_043_0974</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666052">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666052</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267831</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_043_0974</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845627" alias="UCSF_VRP_mNGS_043_0975">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845627</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_043_0975</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666053">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666053</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267832</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_043_0975</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845628" alias="UCSF_VRP_mNGS_043_0976">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845628</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_043_0976</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666054">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666054</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267833</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_043_0976</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845629" alias="UCSF_VRP_mNGS_043_0977">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845629</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_043_0977</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666055">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666055</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267834</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_043_0977</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845630" alias="UCSF_VRP_mNGS_044_0978">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845630</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_044_0978</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666056">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666056</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267835</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_044_0978</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845631" alias="UCSF_VRP_mNGS_044_0979">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845631</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_044_0979</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666057">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666057</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267836</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_044_0979</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845632" alias="UCSF_VRP_mNGS_044_0980">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845632</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_044_0980</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666058">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666058</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267837</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_044_0980</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845633" alias="UCSF_VRP_mNGS_004_0099">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845633</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_004_0099</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666059">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666059</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266956</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_004_0099</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845634" alias="UCSF_VRP_mNGS_044_0981">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845634</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_044_0981</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666060">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666060</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267838</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_044_0981</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845635" alias="UCSF_VRP_mNGS_044_0982">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845635</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_044_0982</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666061">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666061</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267839</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_044_0982</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845636" alias="UCSF_VRP_mNGS_044_0983">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845636</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_044_0983</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666062">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666062</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267840</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_044_0983</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845637" alias="UCSF_VRP_mNGS_044_0984">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845637</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_044_0984</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666063">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666063</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267841</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_044_0984</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845638" alias="UCSF_VRP_mNGS_044_0985">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845638</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_044_0985</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666064">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666064</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267842</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_044_0985</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845639" alias="UCSF_VRP_mNGS_006_0142">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845639</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_006_0142</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666065">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666065</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266999</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_006_0142</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiniSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845640" alias="UCSF_VRP_mNGS_006_0143">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845640</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_006_0143</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666066">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666066</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267000</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_006_0143</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiniSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845641" alias="UCSF_VRP_mNGS_006_0144">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845641</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_006_0144</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666067">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666067</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267001</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_006_0144</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiniSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845642" alias="UCSF_VRP_mNGS_006_0145">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845642</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_006_0145</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666068">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666068</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267002</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_006_0145</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiniSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845643" alias="UCSF_VRP_mNGS_006_0146">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845643</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_006_0146</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666069">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666069</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267003</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_006_0146</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiniSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845644" alias="UCSF_VRP_mNGS_007_0147">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845644</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_007_0147</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666070">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666070</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267004</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_007_0147</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845645" alias="UCSF_VRP_mNGS_007_0148">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845645</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_007_0148</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666071">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666071</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267005</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_007_0148</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845646" alias="UCSF_VRP_mNGS_007_0149">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845646</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_007_0149</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666072">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666072</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267006</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_007_0149</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845647" alias="UCSF_VRP_mNGS_007_0150">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845647</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_007_0150</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666073">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666073</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267007</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_007_0150</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845648" alias="UCSF_VRP_mNGS_001_0016">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845648</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_001_0016</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666074">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666074</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266873</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_001_0016</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845649" alias="UCSF_VRP_mNGS_007_0151">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845649</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_007_0151</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666075">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666075</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267008</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_007_0151</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845650" alias="UCSF_VRP_mNGS_007_0152">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845650</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_007_0152</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666076">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666076</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267009</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_007_0152</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845651" alias="UCSF_VRP_mNGS_007_0153">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845651</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_007_0153</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666077">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666077</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267010</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_007_0153</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845652" alias="UCSF_VRP_mNGS_007_0154">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845652</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_007_0154</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666078">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666078</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267011</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_007_0154</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845653" alias="UCSF_VRP_mNGS_007_0155">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845653</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_007_0155</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666079">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666079</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267012</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_007_0155</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845654" alias="UCSF_VRP_mNGS_007_0156">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845654</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_007_0156</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666080">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666080</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267013</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_007_0156</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845655" alias="UCSF_VRP_mNGS_007_0157">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845655</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_007_0157</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666081">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666081</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267014</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_007_0157</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845656" alias="UCSF_VRP_mNGS_007_0158">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845656</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_007_0158</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666082">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666082</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267015</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_007_0158</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845657" alias="UCSF_VRP_mNGS_007_0159">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845657</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_007_0159</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666083">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666083</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267016</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_007_0159</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845658" alias="UCSF_VRP_mNGS_007_0160">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845658</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_007_0160</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666084">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666084</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267017</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_007_0160</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845659" alias="UCSF_VRP_mNGS_001_0017">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845659</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_001_0017</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666085">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666085</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266874</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_001_0017</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845660" alias="UCSF_VRP_mNGS_007_0161">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845660</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_007_0161</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666086">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666086</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267018</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_007_0161</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845661" alias="UCSF_VRP_mNGS_007_0162">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845661</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_007_0162</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666087">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666087</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267019</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_007_0162</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845662" alias="UCSF_VRP_mNGS_008_0163">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845662</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_008_0163</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666088">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666088</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267020</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_008_0163</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845663" alias="UCSF_VRP_mNGS_013_0294">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845663</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_013_0294</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666089">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666089</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267151</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_013_0294</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845664" alias="UCSF_VRP_mNGS_013_0295">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845664</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_013_0295</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666090">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666090</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267152</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_013_0295</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845665" alias="UCSF_VRP_mNGS_013_0296">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845665</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_013_0296</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666091">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666091</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267153</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_013_0296</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845666" alias="UCSF_VRP_mNGS_013_0297">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845666</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_013_0297</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666092">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666092</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267154</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_013_0297</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845667" alias="UCSF_VRP_mNGS_013_0298">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845667</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_013_0298</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666093">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666093</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267155</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_013_0298</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845668" alias="UCSF_VRP_mNGS_013_0299">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845668</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_013_0299</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666094">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666094</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267156</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_013_0299</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845669" alias="UCSF_VRP_mNGS_013_0300">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845669</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_013_0300</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666095">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666095</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267157</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_013_0300</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845670" alias="UCSF_VRP_mNGS_001_0004">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845670</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_001_0004</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666096">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666096</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266861</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_001_0004</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845671" alias="UCSF_VRP_mNGS_001_0031">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845671</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_001_0031</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666097">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666097</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266888</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_001_0031</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845672" alias="UCSF_VRP_mNGS_013_0301">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845672</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_013_0301</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666098">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666098</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267158</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_013_0301</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845673" alias="UCSF_VRP_mNGS_013_0302">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845673</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_013_0302</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666099">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666099</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267159</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_013_0302</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845674" alias="UCSF_VRP_mNGS_013_0303">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845674</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_013_0303</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666100">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666100</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267160</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_013_0303</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845675" alias="UCSF_VRP_mNGS_013_0304">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845675</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_013_0304</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666101">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666101</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267161</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_013_0304</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845676" alias="UCSF_VRP_mNGS_013_0305">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845676</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_013_0305</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666102">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666102</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267162</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_013_0305</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845677" alias="UCSF_VRP_mNGS_013_0306">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845677</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_013_0306</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666103">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666103</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267163</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_013_0306</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845678" alias="UCSF_VRP_mNGS_013_0307">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845678</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_013_0307</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666104">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666104</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267164</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_013_0307</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845679" alias="UCSF_VRP_mNGS_013_0308">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845679</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_013_0308</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666105">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666105</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267165</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_013_0308</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845680" alias="UCSF_VRP_mNGS_013_0309">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845680</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_013_0309</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666106">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666106</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267166</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_013_0309</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845681" alias="UCSF_VRP_mNGS_013_0310">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845681</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_013_0310</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666107">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666107</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267167</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_013_0310</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845682" alias="UCSF_VRP_mNGS_001_0032">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845682</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_001_0032</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666108">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666108</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266889</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_001_0032</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845683" alias="UCSF_VRP_mNGS_013_0311">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845683</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_013_0311</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666109">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666109</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267168</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_013_0311</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845684" alias="UCSF_VRP_mNGS_013_0312">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845684</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_013_0312</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666110">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666110</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267169</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_013_0312</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845685" alias="UCSF_VRP_mNGS_013_0313">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845685</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_013_0313</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666111">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666111</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267170</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_013_0313</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845686" alias="UCSF_VRP_mNGS_013_0314">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845686</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_013_0314</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666112">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666112</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267171</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_013_0314</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845687" alias="UCSF_VRP_mNGS_015_0359">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845687</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_015_0359</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666113">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666113</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267216</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_015_0359</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845688" alias="UCSF_VRP_mNGS_015_0360">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845688</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_015_0360</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666114">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666114</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267217</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_015_0360</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845689" alias="UCSF_VRP_mNGS_002_0037">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845689</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_002_0037</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666115">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666115</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266894</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_002_0037</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845690" alias="UCSF_VRP_mNGS_015_0361">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845690</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_015_0361</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666116">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666116</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267218</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_015_0361</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845691" alias="UCSF_VRP_mNGS_015_0362">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845691</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_015_0362</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666117">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666117</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267219</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_015_0362</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845692" alias="UCSF_VRP_mNGS_015_0363">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845692</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_015_0363</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666118">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666118</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267220</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_015_0363</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845693" alias="UCSF_VRP_mNGS_015_0364">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845693</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_015_0364</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666119">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666119</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267221</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_015_0364</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845694" alias="UCSF_VRP_mNGS_015_0365">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845694</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_015_0365</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666120">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666120</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267222</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_015_0365</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845695" alias="UCSF_VRP_mNGS_015_0366">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845695</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_015_0366</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666121">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666121</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267223</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_015_0366</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845696" alias="UCSF_VRP_mNGS_015_0367">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845696</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_015_0367</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666122">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666122</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267224</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_015_0367</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845697" alias="UCSF_VRP_mNGS_015_0368">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845697</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_015_0368</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666123">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666123</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267225</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_015_0368</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845698" alias="UCSF_VRP_mNGS_015_0369">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845698</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_015_0369</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666124">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666124</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267226</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_015_0369</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845699" alias="UCSF_VRP_mNGS_015_0370">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845699</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_015_0370</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666125">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666125</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267227</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_015_0370</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845700" alias="UCSF_VRP_mNGS_002_0038">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845700</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_002_0038</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666126">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666126</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266895</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_002_0038</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845701" alias="UCSF_VRP_mNGS_016_0371">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845701</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_016_0371</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666127">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666127</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267228</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_016_0371</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845702" alias="UCSF_VRP_mNGS_016_0372">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845702</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_016_0372</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666128">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666128</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267229</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_016_0372</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845703" alias="UCSF_VRP_mNGS_016_0373">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845703</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_016_0373</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666129">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666129</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267230</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_016_0373</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845704" alias="UCSF_VRP_mNGS_016_0374">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845704</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_016_0374</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666130">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666130</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267231</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_016_0374</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845705" alias="UCSF_VRP_mNGS_016_0375">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845705</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_016_0375</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666131">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666131</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267232</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_016_0375</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845706" alias="UCSF_VRP_mNGS_016_0376">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845706</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_016_0376</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666133">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666133</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267233</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_016_0376</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845707" alias="UCSF_VRP_mNGS_016_0377">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845707</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_016_0377</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666132">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666132</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267234</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_016_0377</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845708" alias="UCSF_VRP_mNGS_016_0378">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845708</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_016_0378</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666135">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666135</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267235</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_016_0378</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845709" alias="UCSF_VRP_mNGS_016_0379">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845709</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_016_0379</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666134">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666134</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267236</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_016_0379</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845710" alias="UCSF_VRP_mNGS_016_0380">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845710</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_016_0380</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666136">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666136</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267237</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_016_0380</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845711" alias="UCSF_VRP_mNGS_018_0423">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845711</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0423</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666137">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666137</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267280</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0423</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845712" alias="UCSF_VRP_mNGS_018_0424">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845712</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0424</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666138">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666138</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267281</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0424</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845713" alias="UCSF_VRP_mNGS_018_0425">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845713</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0425</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666139">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666139</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267282</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0425</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845714" alias="UCSF_VRP_mNGS_018_0426">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845714</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0426</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666140">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666140</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267283</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0426</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845715" alias="UCSF_VRP_mNGS_018_0427">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845715</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0427</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666141">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666141</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267284</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0427</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845716" alias="UCSF_VRP_mNGS_018_0428">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845716</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0428</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666143">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666143</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267285</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0428</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845717" alias="UCSF_VRP_mNGS_018_0429">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845717</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0429</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666142">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666142</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267286</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0429</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845718" alias="UCSF_VRP_mNGS_018_0430">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845718</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0430</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666144">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666144</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267287</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0430</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845719" alias="UCSF_VRP_mNGS_002_0044">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845719</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_002_0044</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666145">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666145</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266901</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_002_0044</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845720" alias="UCSF_VRP_mNGS_018_0431">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845720</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0431</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666146">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666146</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267288</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0431</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845721" alias="UCSF_VRP_mNGS_018_0432">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845721</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0432</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666147">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666147</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267289</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0432</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845722" alias="UCSF_VRP_mNGS_018_0433">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845722</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0433</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666148">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666148</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267290</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0433</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845723" alias="UCSF_VRP_mNGS_018_0434">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845723</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0434</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666149">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666149</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267291</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0434</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845724" alias="UCSF_VRP_mNGS_018_0435">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845724</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0435</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666150">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666150</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267292</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0435</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845725" alias="UCSF_VRP_mNGS_018_0436">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845725</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0436</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666151">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666151</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267293</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0436</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845726" alias="UCSF_VRP_mNGS_018_0437">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845726</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0437</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666153">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666153</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267294</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0437</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845727" alias="UCSF_VRP_mNGS_018_0438">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845727</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0438</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666152">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666152</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267295</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0438</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845728" alias="UCSF_VRP_mNGS_018_0439">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845728</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0439</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666154">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666154</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267296</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0439</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845729" alias="UCSF_VRP_mNGS_018_0440">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845729</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0440</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666155">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666155</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267297</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0440</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845730" alias="UCSF_VRP_mNGS_002_0045">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845730</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_002_0045</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666156">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666156</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266902</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_002_0045</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845731" alias="UCSF_VRP_mNGS_018_0441">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845731</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0441</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666158">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666158</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267298</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0441</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845732" alias="UCSF_VRP_mNGS_018_0442">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845732</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0442</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666157">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666157</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267299</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0442</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845733" alias="UCSF_VRP_mNGS_018_0443">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845733</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0443</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666159">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666159</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267300</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0443</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845734" alias="UCSF_VRP_mNGS_018_0444">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845734</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0444</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666160">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666160</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267301</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0444</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845735" alias="UCSF_VRP_mNGS_019_0489">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845735</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_019_0489</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666161">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666161</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267346</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_019_0489</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845736" alias="UCSF_VRP_mNGS_019_0490">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845736</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_019_0490</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666163">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666163</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267347</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_019_0490</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845737" alias="UCSF_VRP_mNGS_002_0050">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845737</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_002_0050</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666162">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666162</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266907</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_002_0050</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845738" alias="UCSF_VRP_mNGS_019_0491">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845738</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_019_0491</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666164">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666164</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267348</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_019_0491</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845739" alias="UCSF_VRP_mNGS_019_0492">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845739</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_019_0492</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666165">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666165</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267349</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_019_0492</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845740" alias="UCSF_VRP_mNGS_019_0493">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845740</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_019_0493</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666166">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666166</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267350</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_019_0493</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845741" alias="UCSF_VRP_mNGS_019_0494">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845741</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_019_0494</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666168">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666168</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267351</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_019_0494</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845742" alias="UCSF_VRP_mNGS_019_0495">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845742</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_019_0495</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666167">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666167</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267352</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_019_0495</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845743" alias="UCSF_VRP_mNGS_019_0496">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845743</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_019_0496</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666169">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666169</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267353</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_019_0496</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845744" alias="UCSF_VRP_mNGS_019_0497">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845744</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_019_0497</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666171">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666171</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267354</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_019_0497</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845745" alias="UCSF_VRP_mNGS_019_0498">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845745</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_019_0498</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666170">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666170</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267355</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_019_0498</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845746" alias="UCSF_VRP_mNGS_019_0499">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845746</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_019_0499</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666172">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666172</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267356</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_019_0499</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845747" alias="UCSF_VRP_mNGS_020_0500">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845747</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_020_0500</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666173">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666173</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267357</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_020_0500</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845748" alias="UCSF_VRP_mNGS_001_0006">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845748</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_001_0006</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666174">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666174</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266863</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_001_0006</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845749" alias="UCSF_VRP_mNGS_002_0051">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845749</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_002_0051</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666175">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666175</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266908</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_002_0051</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845750" alias="UCSF_VRP_mNGS_020_0501">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845750</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_020_0501</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666176">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666176</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267358</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_020_0501</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845751" alias="UCSF_VRP_mNGS_020_0502">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845751</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_020_0502</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666177">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666177</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267359</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_020_0502</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845752" alias="UCSF_VRP_mNGS_020_0503">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845752</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_020_0503</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666178">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666178</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267360</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_020_0503</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845753" alias="UCSF_VRP_mNGS_020_0504">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845753</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_020_0504</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666179">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666179</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267361</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_020_0504</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845754" alias="UCSF_VRP_mNGS_020_0505">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845754</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_020_0505</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666181">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666181</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267362</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_020_0505</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845755" alias="UCSF_VRP_mNGS_020_0506">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845755</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_020_0506</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666180">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666180</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267363</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_020_0506</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845756" alias="UCSF_VRP_mNGS_020_0507">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845756</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_020_0507</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666182">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666182</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267364</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_020_0507</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845757" alias="UCSF_VRP_mNGS_020_0508">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845757</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_020_0508</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666183">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666183</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267365</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_020_0508</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845758" alias="UCSF_VRP_mNGS_020_0509">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845758</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_020_0509</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666184">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666184</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267366</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_020_0509</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845759" alias="UCSF_VRP_mNGS_023_0553">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845759</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_023_0553</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666185">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666185</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267410</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_023_0553</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845760" alias="UCSF_VRP_mNGS_023_0554">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845760</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_023_0554</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666186">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666186</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267411</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_023_0554</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845761" alias="UCSF_VRP_mNGS_023_0555">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845761</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_023_0555</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666187">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666187</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267412</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_023_0555</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845762" alias="UCSF_VRP_mNGS_023_0556">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845762</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_023_0556</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666188">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666188</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267413</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_023_0556</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845763" alias="UCSF_VRP_mNGS_023_0557">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845763</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_023_0557</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666189">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666189</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267414</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_023_0557</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845764" alias="UCSF_VRP_mNGS_023_0558">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845764</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_023_0558</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666190">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666190</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267415</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_023_0558</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845765" alias="UCSF_VRP_mNGS_023_0559">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845765</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_023_0559</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666192">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666192</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267416</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_023_0559</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845766" alias="UCSF_VRP_mNGS_023_0560">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845766</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_023_0560</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666191">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666191</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267417</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_023_0560</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845767" alias="UCSF_VRP_mNGS_003_0057">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845767</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_003_0057</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666194">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666194</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266914</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_003_0057</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845768" alias="UCSF_VRP_mNGS_023_0561">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845768</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_023_0561</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666193">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666193</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267418</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_023_0561</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845769" alias="UCSF_VRP_mNGS_023_0562">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845769</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_023_0562</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666195">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666195</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267419</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_023_0562</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845770" alias="UCSF_VRP_mNGS_023_0563">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845770</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_023_0563</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666196">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666196</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267420</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_023_0563</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845771" alias="UCSF_VRP_mNGS_023_0564">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845771</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_023_0564</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666199">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666199</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267421</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_023_0564</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845772" alias="UCSF_VRP_mNGS_024_0565">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845772</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_024_0565</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666197">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666197</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267422</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_024_0565</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845773" alias="UCSF_VRP_mNGS_024_0566">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845773</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_024_0566</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666198">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666198</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267423</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_024_0566</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845774" alias="UCSF_VRP_mNGS_024_0567">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845774</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_024_0567</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666200">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666200</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267424</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_024_0567</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845775" alias="UCSF_VRP_mNGS_024_0568">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845775</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_024_0568</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666201">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666201</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267425</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_024_0568</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845776" alias="UCSF_VRP_mNGS_024_0569">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845776</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_024_0569</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666202">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666202</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267426</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_024_0569</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845777" alias="UCSF_VRP_mNGS_024_0570">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845777</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_024_0570</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666203">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666203</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267427</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_024_0570</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845778" alias="UCSF_VRP_mNGS_003_0058">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845778</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_003_0058</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666204">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666204</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266915</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_003_0058</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845779" alias="UCSF_VRP_mNGS_024_0571">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845779</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_024_0571</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666205">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666205</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267428</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_024_0571</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845780" alias="UCSF_VRP_mNGS_024_0572">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845780</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_024_0572</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666206">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666206</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267429</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_024_0572</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845781" alias="UCSF_VRP_mNGS_024_0573">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845781</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_024_0573</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666208">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666208</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267430</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_024_0573</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845782" alias="UCSF_VRP_mNGS_024_0574">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845782</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_024_0574</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666207">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666207</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267431</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_024_0574</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845783" alias="UCSF_VRP_mNGS_031_0704">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845783</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_031_0704</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666209">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666209</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267561</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_031_0704</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845784" alias="UCSF_VRP_mNGS_031_0705">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845784</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_031_0705</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666211">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666211</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267562</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_031_0705</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845785" alias="UCSF_VRP_mNGS_031_0706">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845785</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_031_0706</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666214">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666214</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267563</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_031_0706</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845786" alias="UCSF_VRP_mNGS_031_0707">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845786</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_031_0707</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666210">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666210</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267564</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_031_0707</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845787" alias="UCSF_VRP_mNGS_031_0708">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845787</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_031_0708</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666212">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666212</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267565</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_031_0708</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845788" alias="UCSF_VRP_mNGS_031_0709">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845788</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_031_0709</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666213">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666213</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267566</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_031_0709</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845789" alias="UCSF_VRP_mNGS_031_0710">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845789</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_031_0710</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666215">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666215</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267567</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_031_0710</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845790" alias="UCSF_VRP_mNGS_003_0072">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845790</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_003_0072</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666216">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666216</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266929</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_003_0072</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845791" alias="UCSF_VRP_mNGS_031_0711">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845791</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_031_0711</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666218">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666218</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267568</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_031_0711</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845792" alias="UCSF_VRP_mNGS_031_0712">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845792</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_031_0712</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666217">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666217</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267569</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_031_0712</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845793" alias="UCSF_VRP_mNGS_031_0713">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845793</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_031_0713</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666219">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666219</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267570</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_031_0713</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845794" alias="UCSF_VRP_mNGS_031_0714">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845794</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_031_0714</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666220">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666220</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267571</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_031_0714</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845795" alias="UCSF_VRP_mNGS_031_0715">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845795</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_031_0715</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666221">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666221</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267572</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_031_0715</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845796" alias="UCSF_VRP_mNGS_031_0716">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845796</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_031_0716</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666223">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666223</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267573</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_031_0716</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845797" alias="UCSF_VRP_mNGS_031_0717">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845797</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_031_0717</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666222">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666222</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267574</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_031_0717</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845798" alias="UCSF_VRP_mNGS_031_0718">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845798</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_031_0718</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666225">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666225</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267575</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_031_0718</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845799" alias="UCSF_VRP_mNGS_031_0719">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845799</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_031_0719</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666224">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666224</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267576</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_031_0719</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845800" alias="UCSF_VRP_mNGS_031_0720">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845800</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_031_0720</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666226">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666226</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267577</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_031_0720</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845801" alias="UCSF_VRP_mNGS_003_0073">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845801</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_003_0073</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666227">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666227</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266930</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_003_0073</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845802" alias="UCSF_VRP_mNGS_032_0721">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845802</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_032_0721</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666228">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666228</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267578</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_032_0721</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845803" alias="UCSF_VRP_mNGS_032_0722">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845803</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_032_0722</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666229">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666229</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267579</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_032_0722</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845804" alias="UCSF_VRP_mNGS_032_0723">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845804</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_032_0723</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666230">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666230</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267580</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_032_0723</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845805" alias="UCSF_VRP_mNGS_032_0724">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845805</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_032_0724</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666232">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666232</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267581</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_032_0724</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845806" alias="UCSF_VRP_mNGS_032_0725">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845806</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_032_0725</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666231">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666231</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267582</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_032_0725</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845807" alias="UCSF_VRP_mNGS_037_0856">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845807</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_037_0856</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666233">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666233</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267713</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_037_0856</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845808" alias="UCSF_VRP_mNGS_037_0857">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845808</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_037_0857</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666234">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666234</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267714</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_037_0857</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845809" alias="UCSF_VRP_mNGS_037_0858">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845809</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_037_0858</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666235">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666235</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267715</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_037_0858</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845810" alias="UCSF_VRP_mNGS_037_0859">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845810</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_037_0859</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666236">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666236</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267716</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_037_0859</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845811" alias="UCSF_VRP_mNGS_038_0860">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845811</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_038_0860</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666237">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666237</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267717</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_038_0860</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845812" alias="UCSF_VRP_mNGS_004_0087">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845812</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_004_0087</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666239">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666239</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266944</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_004_0087</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845813" alias="UCSF_VRP_mNGS_038_0861">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845813</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_038_0861</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666238">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666238</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267718</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_038_0861</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845814" alias="UCSF_VRP_mNGS_038_0862">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845814</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_038_0862</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666241">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666241</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267719</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_038_0862</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845815" alias="UCSF_VRP_mNGS_038_0863">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845815</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_038_0863</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666240">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666240</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267720</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_038_0863</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845816" alias="UCSF_VRP_mNGS_038_0864">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845816</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_038_0864</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666242">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666242</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267721</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_038_0864</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845817" alias="UCSF_VRP_mNGS_038_0865">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845817</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_038_0865</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666243">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666243</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267722</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_038_0865</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845818" alias="UCSF_VRP_mNGS_038_0866">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845818</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_038_0866</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666244">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666244</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267723</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_038_0866</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845819" alias="UCSF_VRP_mNGS_038_0867">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845819</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_038_0867</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666245">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666245</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267724</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_038_0867</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845820" alias="UCSF_VRP_mNGS_039_0868">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845820</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_039_0868</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666246">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666246</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267725</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_039_0868</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845821" alias="UCSF_VRP_mNGS_039_0869">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845821</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_039_0869</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666247">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666247</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267726</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_039_0869</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845822" alias="UCSF_VRP_mNGS_039_0870">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845822</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_039_0870</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666249">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666249</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267727</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_039_0870</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845823" alias="UCSF_VRP_mNGS_004_0088">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845823</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_004_0088</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666248">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666248</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266945</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_004_0088</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845824" alias="UCSF_VRP_mNGS_039_0871">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845824</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_039_0871</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666250">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666250</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267728</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_039_0871</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845825" alias="UCSF_VRP_mNGS_039_0872">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845825</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_039_0872</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666251">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666251</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267729</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_039_0872</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845826" alias="UCSF_VRP_mNGS_039_0873">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845826</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_039_0873</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666254">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666254</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267730</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_039_0873</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845827" alias="UCSF_VRP_mNGS_039_0874">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845827</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_039_0874</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666252">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666252</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267731</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_039_0874</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845828" alias="UCSF_VRP_mNGS_039_0875">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845828</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_039_0875</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666253">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666253</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267732</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_039_0875</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845829" alias="UCSF_VRP_mNGS_039_0876">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845829</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_039_0876</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666255">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666255</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267733</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_039_0876</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845830" alias="UCSF_VRP_mNGS_039_0877">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845830</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_039_0877</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666256">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666256</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267734</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_039_0877</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845831" alias="UCSF_VRP_mNGS_008_0164">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845831</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_008_0164</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666257">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666257</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267021</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_008_0164</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845832" alias="UCSF_VRP_mNGS_008_0165">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845832</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_008_0165</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666258">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666258</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267022</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_008_0165</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845833" alias="UCSF_VRP_mNGS_008_0166">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845833</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_008_0166</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666260">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666260</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267023</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_008_0166</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845834" alias="UCSF_VRP_mNGS_008_0167">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845834</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_008_0167</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666259">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666259</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267024</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_008_0167</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845835" alias="UCSF_VRP_mNGS_008_0168">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845835</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_008_0168</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666261">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666261</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267025</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_008_0168</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845836" alias="UCSF_VRP_mNGS_008_0169">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845836</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_008_0169</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666263">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666263</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267026</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_008_0169</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845837" alias="UCSF_VRP_mNGS_008_0170">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845837</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_008_0170</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666262">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666262</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267027</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_008_0170</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845838" alias="UCSF_VRP_mNGS_001_0018">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845838</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_001_0018</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666264">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666264</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266875</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_001_0018</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845839" alias="UCSF_VRP_mNGS_008_0171">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845839</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_008_0171</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666266">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666266</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267028</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_008_0171</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845840" alias="UCSF_VRP_mNGS_008_0172">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845840</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_008_0172</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666265">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666265</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267029</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_008_0172</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845841" alias="UCSF_VRP_mNGS_008_0173">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845841</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_008_0173</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666267">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666267</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267030</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_008_0173</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845842" alias="UCSF_VRP_mNGS_008_0174">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845842</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_008_0174</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666268">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666268</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267031</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_008_0174</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845843" alias="UCSF_VRP_mNGS_008_0175">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845843</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_008_0175</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666269">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666269</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267032</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_008_0175</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845844" alias="UCSF_VRP_mNGS_008_0176">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845844</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_008_0176</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666270">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666270</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267033</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_008_0176</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845845" alias="UCSF_VRP_mNGS_008_0177">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845845</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_008_0177</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666271">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666271</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267034</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_008_0177</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845846" alias="UCSF_VRP_mNGS_008_0178">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845846</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_008_0178</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666272">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666272</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267035</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_008_0178</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845847" alias="UCSF_VRP_mNGS_009_0179">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845847</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_009_0179</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666273">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666273</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267036</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_009_0179</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845848" alias="UCSF_VRP_mNGS_009_0180">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845848</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_009_0180</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666274">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666274</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267037</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_009_0180</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845849" alias="UCSF_VRP_mNGS_001_0019">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845849</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_001_0019</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666275">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666275</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266876</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_001_0019</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845850" alias="UCSF_VRP_mNGS_009_0181">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845850</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_009_0181</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666277">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666277</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267038</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_009_0181</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845851" alias="UCSF_VRP_mNGS_009_0182">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845851</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_009_0182</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666276">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666276</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267039</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_009_0182</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845852" alias="UCSF_VRP_mNGS_009_0183">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845852</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_009_0183</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666279">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666279</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267040</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_009_0183</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845853" alias="UCSF_VRP_mNGS_009_0184">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845853</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_009_0184</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666278">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666278</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267041</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_009_0184</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845854" alias="UCSF_VRP_mNGS_009_0185">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845854</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_009_0185</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666280">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666280</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267042</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_009_0185</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845855" alias="UCSF_VRP_mNGS_011_0229">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845855</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_011_0229</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666281">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666281</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267086</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_011_0229</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845856" alias="UCSF_VRP_mNGS_011_0230">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845856</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_011_0230</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666282">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666282</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267087</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_011_0230</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845857" alias="UCSF_VRP_mNGS_001_0024">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845857</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_001_0024</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666283">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666283</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266881</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_001_0024</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845858" alias="UCSF_VRP_mNGS_011_0231">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845858</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_011_0231</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666284">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666284</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267088</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_011_0231</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845859" alias="UCSF_VRP_mNGS_011_0232">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845859</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_011_0232</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666285">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666285</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267089</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_011_0232</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845860" alias="UCSF_VRP_mNGS_011_0233">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845860</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_011_0233</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666286">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666286</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267090</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_011_0233</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845861" alias="UCSF_VRP_mNGS_011_0234">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845861</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_011_0234</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666288">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666288</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267091</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_011_0234</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845862" alias="UCSF_VRP_mNGS_011_0235">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845862</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_011_0235</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666287">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666287</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267092</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_011_0235</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845863" alias="UCSF_VRP_mNGS_011_0236">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845863</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_011_0236</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666289">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666289</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267093</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_011_0236</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845864" alias="UCSF_VRP_mNGS_011_0237">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845864</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_011_0237</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666290">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666290</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267094</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_011_0237</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845865" alias="UCSF_VRP_mNGS_011_0238">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845865</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_011_0238</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666294">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666294</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267095</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_011_0238</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845866" alias="UCSF_VRP_mNGS_011_0239">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845866</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_011_0239</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666293">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666293</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267096</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_011_0239</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845867" alias="UCSF_VRP_mNGS_011_0240">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845867</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_011_0240</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666291">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666291</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267097</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_011_0240</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845868" alias="UCSF_VRP_mNGS_001_0025">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845868</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_001_0025</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666292">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666292</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266882</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_001_0025</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845869" alias="UCSF_VRP_mNGS_011_0241">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845869</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_011_0241</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666295">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666295</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267098</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_011_0241</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845870" alias="UCSF_VRP_mNGS_011_0242">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845870</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_011_0242</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666296">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666296</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267099</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_011_0242</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845871" alias="UCSF_VRP_mNGS_011_0243">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845871</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_011_0243</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666298">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666298</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267100</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_011_0243</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845872" alias="UCSF_VRP_mNGS_011_0244">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845872</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_011_0244</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666297">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666297</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267101</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_011_0244</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845873" alias="UCSF_VRP_mNGS_011_0245">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845873</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_011_0245</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666299">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666299</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267102</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_011_0245</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845874" alias="UCSF_VRP_mNGS_011_0246">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845874</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_011_0246</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666300">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666300</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267103</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_011_0246</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845875" alias="UCSF_VRP_mNGS_011_0247">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845875</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_011_0247</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666301">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666301</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267104</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_011_0247</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845876" alias="UCSF_VRP_mNGS_011_0248">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845876</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_011_0248</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666302">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666302</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267105</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_011_0248</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845877" alias="UCSF_VRP_mNGS_011_0249">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845877</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_011_0249</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666304">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666304</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267106</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_011_0249</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845878" alias="UCSF_VRP_mNGS_011_0250">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845878</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_011_0250</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666303">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666303</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267107</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_011_0250</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845879" alias="UCSF_VRP_mNGS_014_0315">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845879</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_014_0315</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666305">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666305</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267172</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_014_0315</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845880" alias="UCSF_VRP_mNGS_014_0316">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845880</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_014_0316</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666307">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666307</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267173</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_014_0316</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845881" alias="UCSF_VRP_mNGS_014_0317">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845881</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_014_0317</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666306">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666306</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267174</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_014_0317</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845882" alias="UCSF_VRP_mNGS_014_0318">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845882</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_014_0318</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666308">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666308</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267175</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_014_0318</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845883" alias="UCSF_VRP_mNGS_014_0319">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845883</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_014_0319</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666311">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666311</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267176</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_014_0319</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845884" alias="UCSF_VRP_mNGS_014_0320">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845884</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_014_0320</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666309">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666309</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267177</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_014_0320</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845885" alias="UCSF_VRP_mNGS_001_0033">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845885</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_001_0033</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666312">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666312</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266890</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_001_0033</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845886" alias="UCSF_VRP_mNGS_014_0321">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845886</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_014_0321</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666310">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666310</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267178</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_014_0321</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845887" alias="UCSF_VRP_mNGS_014_0322">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845887</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_014_0322</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666313">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666313</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267179</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_014_0322</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845888" alias="UCSF_VRP_mNGS_014_0323">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845888</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_014_0323</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666314">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666314</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267180</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_014_0323</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845889" alias="UCSF_VRP_mNGS_014_0324">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845889</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_014_0324</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666316">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666316</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267181</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_014_0324</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845890" alias="UCSF_VRP_mNGS_014_0325">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845890</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_014_0325</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666315">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666315</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267182</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_014_0325</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845891" alias="UCSF_VRP_mNGS_014_0326">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845891</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_014_0326</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666317">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666317</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267183</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_014_0326</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845892" alias="UCSF_VRP_mNGS_014_0327">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845892</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_014_0327</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666318">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666318</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267184</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_014_0327</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845893" alias="UCSF_VRP_mNGS_014_0328">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845893</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_014_0328</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666319">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666319</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267185</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_014_0328</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845894" alias="UCSF_VRP_mNGS_014_0329">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845894</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_014_0329</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666320">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666320</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267186</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_014_0329</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845895" alias="UCSF_VRP_mNGS_014_0330">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845895</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_014_0330</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666321">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666321</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267187</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_014_0330</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845896" alias="UCSF_VRP_mNGS_002_0034">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845896</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_002_0034</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666322">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666322</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266891</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_002_0034</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845897" alias="UCSF_VRP_mNGS_014_0331">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845897</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_014_0331</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666324">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666324</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267188</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_014_0331</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845898" alias="UCSF_VRP_mNGS_014_0332">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845898</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_014_0332</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666325">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666325</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267189</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_014_0332</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845899" alias="UCSF_VRP_mNGS_014_0333">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845899</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_014_0333</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666323">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666323</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267190</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_014_0333</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845900" alias="UCSF_VRP_mNGS_014_0334">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845900</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_014_0334</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666326">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666326</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267191</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_014_0334</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845901" alias="UCSF_VRP_mNGS_014_0335">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845901</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_014_0335</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666327">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666327</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267192</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_014_0335</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845902" alias="UCSF_VRP_mNGS_014_0336">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845902</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_014_0336</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666329">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666329</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267193</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_014_0336</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845903" alias="UCSF_VRP_mNGS_026_0618">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845903</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_026_0618</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666330">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666330</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267475</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_026_0618</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845904" alias="UCSF_VRP_mNGS_026_0619">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845904</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_026_0619</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666328">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666328</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267476</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_026_0619</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845905" alias="UCSF_VRP_mNGS_026_0620">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845905</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_026_0620</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666331">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666331</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267477</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_026_0620</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845906" alias="UCSF_VRP_mNGS_003_0063">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845906</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_003_0063</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666332">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666332</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266920</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_003_0063</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845907" alias="UCSF_VRP_mNGS_027_0621">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845907</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_027_0621</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666333">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666333</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267478</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_027_0621</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845908" alias="UCSF_VRP_mNGS_027_0622">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845908</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_027_0622</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666334">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666334</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267479</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_027_0622</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845909" alias="UCSF_VRP_mNGS_027_0623">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845909</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_027_0623</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666335">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666335</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267480</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_027_0623</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845910" alias="UCSF_VRP_mNGS_027_0624">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845910</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_027_0624</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666336">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666336</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267481</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_027_0624</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845911" alias="UCSF_VRP_mNGS_027_0625">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845911</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_027_0625</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666338">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666338</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267482</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_027_0625</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845912" alias="UCSF_VRP_mNGS_027_0626">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845912</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_027_0626</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666339">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666339</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267483</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_027_0626</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845913" alias="UCSF_VRP_mNGS_027_0627">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845913</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_027_0627</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666337">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666337</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267484</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_027_0627</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845914" alias="UCSF_VRP_mNGS_027_0628">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845914</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_027_0628</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666340">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666340</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267485</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_027_0628</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845915" alias="UCSF_VRP_mNGS_027_0629">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845915</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_027_0629</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666341">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666341</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267486</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_027_0629</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845916" alias="UCSF_VRP_mNGS_027_0630">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845916</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_027_0630</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666342">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666342</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267487</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_027_0630</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845917" alias="UCSF_VRP_mNGS_003_0064">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845917</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_003_0064</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666344">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666344</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266921</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_003_0064</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845918" alias="UCSF_VRP_mNGS_027_0631">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845918</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_027_0631</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666343">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666343</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267488</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_027_0631</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845919" alias="UCSF_VRP_mNGS_027_0632">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845919</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_027_0632</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666345">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666345</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267489</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_027_0632</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845920" alias="UCSF_VRP_mNGS_027_0633">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845920</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_027_0633</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666347">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666347</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267490</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_027_0633</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845921" alias="UCSF_VRP_mNGS_027_0634">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845921</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_027_0634</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666346">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666346</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267491</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_027_0634</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845922" alias="UCSF_VRP_mNGS_027_0635">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845922</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_027_0635</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666348">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666348</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267492</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_027_0635</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845923" alias="UCSF_VRP_mNGS_027_0636">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845923</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_027_0636</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666349">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666349</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267493</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_027_0636</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845924" alias="UCSF_VRP_mNGS_027_0637">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845924</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_027_0637</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666350">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666350</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267494</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_027_0637</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845925" alias="UCSF_VRP_mNGS_027_0638">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845925</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_027_0638</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666353">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666353</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267495</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_027_0638</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845926" alias="UCSF_VRP_mNGS_027_0639">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845926</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_027_0639</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666352">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666352</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267496</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_027_0639</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845927" alias="UCSF_VRP_mNGS_029_0661">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845927</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_029_0661</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666351">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666351</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267518</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_029_0661</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845928" alias="UCSF_VRP_mNGS_029_0662">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845928</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_029_0662</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666354">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666354</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267519</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_029_0662</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845929" alias="UCSF_VRP_mNGS_029_0663">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845929</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_029_0663</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666355">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666355</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267520</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_029_0663</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845930" alias="UCSF_VRP_mNGS_029_0664">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845930</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_029_0664</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666356">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666356</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267521</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_029_0664</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845931" alias="UCSF_VRP_mNGS_029_0665">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845931</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_029_0665</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666358">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666358</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267522</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_029_0665</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845932" alias="UCSF_VRP_mNGS_029_0666">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845932</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_029_0666</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666357">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666357</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267523</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_029_0666</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845933" alias="UCSF_VRP_mNGS_029_0667">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845933</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_029_0667</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666359">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666359</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267524</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_029_0667</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845934" alias="UCSF_VRP_mNGS_029_0668">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845934</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_029_0668</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666361">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666361</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267525</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_029_0668</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845935" alias="UCSF_VRP_mNGS_029_0669">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845935</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_029_0669</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666360">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666360</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267526</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_029_0669</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845936" alias="UCSF_VRP_mNGS_029_0670">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845936</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_029_0670</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666362">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666362</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267527</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_029_0670</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845937" alias="UCSF_VRP_mNGS_003_0068">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845937</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_003_0068</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666363">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666363</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266925</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_003_0068</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845938" alias="UCSF_VRP_mNGS_029_0671">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845938</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_029_0671</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666364">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666364</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267528</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_029_0671</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845939" alias="UCSF_VRP_mNGS_029_0672">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845939</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_029_0672</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666365">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666365</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267529</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_029_0672</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845940" alias="UCSF_VRP_mNGS_029_0673">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845940</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_029_0673</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666367">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666367</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267530</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_029_0673</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845941" alias="UCSF_VRP_mNGS_029_0674">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845941</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_029_0674</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666366">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666366</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267531</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_029_0674</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845942" alias="UCSF_VRP_mNGS_029_0675">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845942</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_029_0675</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666368">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666368</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267532</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_029_0675</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845943" alias="UCSF_VRP_mNGS_029_0676">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845943</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_029_0676</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666370">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666370</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267533</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_029_0676</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845944" alias="UCSF_VRP_mNGS_030_0677">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845944</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_030_0677</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666369">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666369</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267534</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_030_0677</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845945" alias="UCSF_VRP_mNGS_030_0678">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845945</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_030_0678</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666371">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666371</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267535</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_030_0678</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845946" alias="UCSF_VRP_mNGS_030_0679">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845946</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_030_0679</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666372">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666372</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267536</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_030_0679</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845947" alias="UCSF_VRP_mNGS_030_0680">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845947</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_030_0680</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666373">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666373</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267537</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_030_0680</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845948" alias="UCSF_VRP_mNGS_003_0069">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845948</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_003_0069</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666374">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666374</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266926</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_003_0069</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845949" alias="UCSF_VRP_mNGS_030_0681">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845949</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_030_0681</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666375">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666375</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267538</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_030_0681</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845950" alias="UCSF_VRP_mNGS_030_0682">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845950</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_030_0682</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666376">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666376</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267539</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_030_0682</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845951" alias="UCSF_VRP_mNGS_032_0726">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845951</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_032_0726</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666377">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666377</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267583</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_032_0726</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845952" alias="UCSF_VRP_mNGS_032_0727">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845952</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_032_0727</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666379">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666379</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267584</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_032_0727</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845953" alias="UCSF_VRP_mNGS_032_0728">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845953</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_032_0728</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666380">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666380</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267585</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_032_0728</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845954" alias="UCSF_VRP_mNGS_032_0729">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845954</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_032_0729</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666378">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666378</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267586</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_032_0729</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845955" alias="UCSF_VRP_mNGS_032_0730">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845955</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_032_0730</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666381">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666381</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267587</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_032_0730</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845956" alias="UCSF_VRP_mNGS_003_0074">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845956</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_003_0074</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666382">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666382</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266931</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_003_0074</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845957" alias="UCSF_VRP_mNGS_032_0731">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845957</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_032_0731</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666383">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666383</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267588</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_032_0731</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845958" alias="UCSF_VRP_mNGS_032_0732">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845958</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_032_0732</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666385">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666385</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267589</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_032_0732</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845959" alias="UCSF_VRP_mNGS_032_0733">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845959</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_032_0733</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666384">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666384</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267590</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_032_0733</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845960" alias="UCSF_VRP_mNGS_032_0734">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845960</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_032_0734</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666386">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666386</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267591</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_032_0734</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845961" alias="UCSF_VRP_mNGS_032_0735">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845961</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_032_0735</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666387">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666387</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267592</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_032_0735</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845962" alias="UCSF_VRP_mNGS_032_0736">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845962</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_032_0736</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666388">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666388</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267593</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_032_0736</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845963" alias="UCSF_VRP_mNGS_033_0737">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845963</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_033_0737</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666389">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666389</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267594</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_033_0737</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845964" alias="UCSF_VRP_mNGS_033_0738">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845964</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_033_0738</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666390">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666390</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267595</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_033_0738</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845965" alias="UCSF_VRP_mNGS_033_0739">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845965</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_033_0739</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666391">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666391</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267596</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_033_0739</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845966" alias="UCSF_VRP_mNGS_033_0740">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845966</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_033_0740</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666392">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666392</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267597</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_033_0740</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845967" alias="UCSF_VRP_mNGS_003_0075">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845967</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_003_0075</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666395">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666395</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266932</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_003_0075</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845968" alias="UCSF_VRP_mNGS_033_0741">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845968</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_033_0741</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666393">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666393</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267598</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_033_0741</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845969" alias="UCSF_VRP_mNGS_033_0742">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845969</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_033_0742</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666394">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666394</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267599</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_033_0742</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845970" alias="UCSF_VRP_mNGS_033_0743">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845970</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_033_0743</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666396">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666396</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267600</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_033_0743</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845971" alias="UCSF_VRP_mNGS_033_0744">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845971</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_033_0744</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666397">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666397</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267601</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_033_0744</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845972" alias="UCSF_VRP_mNGS_033_0745">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845972</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_033_0745</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666398">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666398</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267602</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_033_0745</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845973" alias="UCSF_VRP_mNGS_033_0746">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845973</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_033_0746</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666399">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666399</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267603</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_033_0746</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845974" alias="UCSF_VRP_mNGS_033_0747">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845974</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_033_0747</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666400">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666400</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267604</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_033_0747</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845975" alias="UCSF_VRP_mNGS_035_0791">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845975</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_035_0791</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666402">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666402</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267648</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_035_0791</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845976" alias="UCSF_VRP_mNGS_035_0792">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845976</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_035_0792</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666401">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666401</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267649</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_035_0792</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845977" alias="UCSF_VRP_mNGS_035_0793">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845977</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_035_0793</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666404">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666404</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267650</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_035_0793</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845978" alias="UCSF_VRP_mNGS_035_0794">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845978</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_035_0794</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666403">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666403</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267651</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_035_0794</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845979" alias="UCSF_VRP_mNGS_035_0795">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845979</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_035_0795</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666405">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666405</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267652</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_035_0795</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845980" alias="UCSF_VRP_mNGS_035_0796">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845980</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_035_0796</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666406">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666406</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267653</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_035_0796</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845981" alias="UCSF_VRP_mNGS_035_0797">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845981</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_035_0797</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666407">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666407</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267654</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_035_0797</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845982" alias="UCSF_VRP_mNGS_035_0798">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845982</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_035_0798</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666409">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666409</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267655</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_035_0798</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845983" alias="UCSF_VRP_mNGS_035_0799">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845983</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_035_0799</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666408">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666408</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267656</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_035_0799</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845984" alias="UCSF_VRP_mNGS_035_0800">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845984</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_035_0800</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666411">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666411</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267657</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_035_0800</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845985" alias="UCSF_VRP_mNGS_001_0009">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845985</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_001_0009</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666410">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666410</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266866</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_001_0009</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845986" alias="UCSF_VRP_mNGS_003_0081">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845986</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_003_0081</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666412">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666412</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266938</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_003_0081</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845987" alias="UCSF_VRP_mNGS_035_0801">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845987</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_035_0801</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666413">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666413</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267658</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_035_0801</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845988" alias="UCSF_VRP_mNGS_035_0802">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845988</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_035_0802</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666414">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666414</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267659</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_035_0802</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845989" alias="UCSF_VRP_mNGS_035_0803">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845989</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_035_0803</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666415">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666415</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267660</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_035_0803</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845990" alias="UCSF_VRP_mNGS_035_0804">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845990</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_035_0804</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666416">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666416</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267661</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_035_0804</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845991" alias="UCSF_VRP_mNGS_035_0805">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845991</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_035_0805</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666417">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666417</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267662</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_035_0805</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845992" alias="UCSF_VRP_mNGS_035_0806">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845992</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_035_0806</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666418">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666418</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267663</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_035_0806</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845993" alias="UCSF_VRP_mNGS_035_0807">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845993</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_035_0807</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666419">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666419</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267664</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_035_0807</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845994" alias="UCSF_VRP_mNGS_035_0808">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845994</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_035_0808</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666420">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666420</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267665</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_035_0808</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845995" alias="UCSF_VRP_mNGS_035_0809">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845995</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_035_0809</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666422">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666422</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267666</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_035_0809</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845996" alias="UCSF_VRP_mNGS_036_0810">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845996</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_036_0810</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666421">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666421</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267667</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_036_0810</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845997" alias="UCSF_VRP_mNGS_003_0082">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845997</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_003_0082</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666424">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666424</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266939</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_003_0082</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845998" alias="UCSF_VRP_mNGS_036_0811">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845998</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_036_0811</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666423">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666423</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267668</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_036_0811</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23845999" alias="UCSF_VRP_mNGS_039_0878">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23845999</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_039_0878</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666429">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666429</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267735</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_039_0878</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846000" alias="UCSF_VRP_mNGS_039_0879">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846000</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_039_0879</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666425">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666425</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267736</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_039_0879</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846001" alias="UCSF_VRP_mNGS_039_0880">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846001</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_039_0880</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666428">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666428</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267737</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_039_0880</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846002" alias="UCSF_VRP_mNGS_004_0089">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846002</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_004_0089</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666426">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666426</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266946</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_004_0089</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846003" alias="UCSF_VRP_mNGS_039_0881">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846003</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_039_0881</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666427">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666427</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267738</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_039_0881</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846004" alias="UCSF_VRP_mNGS_039_0882">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846004</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_039_0882</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666432">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666432</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267739</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_039_0882</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846005" alias="UCSF_VRP_mNGS_039_0883">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846005</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_039_0883</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666433">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666433</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267740</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_039_0883</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846006" alias="UCSF_VRP_mNGS_039_0884">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846006</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_039_0884</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666430">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666430</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267741</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_039_0884</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846007" alias="UCSF_VRP_mNGS_039_0885">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846007</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_039_0885</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666431">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666431</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267742</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_039_0885</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846008" alias="UCSF_VRP_mNGS_039_0886">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846008</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_039_0886</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666434">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666434</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267743</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_039_0886</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846009" alias="UCSF_VRP_mNGS_039_0887">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846009</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_039_0887</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666437">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666437</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267744</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_039_0887</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846010" alias="UCSF_VRP_mNGS_039_0888">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846010</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_039_0888</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666435">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666435</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267745</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_039_0888</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846011" alias="UCSF_VRP_mNGS_039_0889">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846011</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_039_0889</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666436">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666436</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267746</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_039_0889</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846012" alias="UCSF_VRP_mNGS_039_0890">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846012</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_039_0890</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666438">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666438</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267747</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_039_0890</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846013" alias="UCSF_VRP_mNGS_004_0090">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846013</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_004_0090</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666441">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666441</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266947</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_004_0090</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846014" alias="UCSF_VRP_mNGS_039_0891">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846014</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_039_0891</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666439">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666439</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267748</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_039_0891</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846015" alias="UCSF_VRP_mNGS_040_0892">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846015</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_040_0892</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666440">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666440</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267749</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_040_0892</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846016" alias="UCSF_VRP_mNGS_040_0893">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846016</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_040_0893</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666442">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666442</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267750</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_040_0893</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846017" alias="UCSF_VRP_mNGS_040_0894">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846017</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_040_0894</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666444">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666444</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267751</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_040_0894</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846018" alias="UCSF_VRP_mNGS_040_0895">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846018</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_040_0895</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666443">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666443</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267752</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_040_0895</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846019" alias="UCSF_VRP_mNGS_040_0896">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846019</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_040_0896</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666445">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666445</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267753</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_040_0896</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846020" alias="UCSF_VRP_mNGS_040_0897">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846020</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_040_0897</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666448">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666448</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267754</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_040_0897</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846021" alias="UCSF_VRP_mNGS_040_0898">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846021</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_040_0898</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666446">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666446</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267755</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_040_0898</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846022" alias="UCSF_VRP_mNGS_040_0899">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846022</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_040_0899</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666447">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666447</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267756</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_040_0899</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846023" alias="UCSF_VRP_mNGS_004_0093">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846023</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_004_0093</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666449">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666449</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266950</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_004_0093</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846024" alias="UCSF_VRP_mNGS_041_0921">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846024</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_041_0921</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666450">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666450</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267778</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_041_0921</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846025" alias="UCSF_VRP_mNGS_041_0922">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846025</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_041_0922</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666452">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666452</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267779</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_041_0922</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846026" alias="UCSF_VRP_mNGS_041_0923">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846026</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_041_0923</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666451">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666451</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267780</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_041_0923</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846027" alias="UCSF_VRP_mNGS_041_0924">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846027</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_041_0924</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666454">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666454</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267781</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_041_0924</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846028" alias="UCSF_VRP_mNGS_041_0925">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846028</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_041_0925</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666453">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666453</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267782</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_041_0925</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846029" alias="UCSF_VRP_mNGS_041_0926">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846029</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_041_0926</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666456">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666456</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267783</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_041_0926</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846030" alias="UCSF_VRP_mNGS_041_0927">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846030</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_041_0927</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666455">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666455</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267784</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_041_0927</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846031" alias="UCSF_VRP_mNGS_041_0928">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846031</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_041_0928</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666458">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666458</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267785</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_041_0928</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846032" alias="UCSF_VRP_mNGS_041_0929">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846032</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_041_0929</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666457">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666457</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267786</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_041_0929</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846033" alias="UCSF_VRP_mNGS_041_0930">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846033</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_041_0930</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666459">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666459</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267787</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_041_0930</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846034" alias="UCSF_VRP_mNGS_004_0094">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846034</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_004_0094</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666460">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666460</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266951</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_004_0094</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846035" alias="UCSF_VRP_mNGS_041_0931">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846035</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_041_0931</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666463">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666463</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267788</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_041_0931</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846036" alias="UCSF_VRP_mNGS_042_0932">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846036</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_042_0932</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666461">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666461</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267789</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_042_0932</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846037" alias="UCSF_VRP_mNGS_042_0933">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846037</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_042_0933</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666462">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666462</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267790</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_042_0933</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846038" alias="UCSF_VRP_mNGS_042_0934">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846038</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_042_0934</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666464">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666464</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267791</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_042_0934</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846039" alias="UCSF_VRP_mNGS_042_0935">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846039</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_042_0935</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666465">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666465</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267792</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_042_0935</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846040" alias="UCSF_VRP_mNGS_042_0936">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846040</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_042_0936</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666466">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666466</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267793</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_042_0936</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846041" alias="UCSF_VRP_mNGS_042_0937">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846041</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_042_0937</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666467">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666467</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267794</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_042_0937</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846042" alias="UCSF_VRP_mNGS_042_0938">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846042</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_042_0938</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666468">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666468</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267795</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_042_0938</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846043" alias="UCSF_VRP_mNGS_042_0939">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846043</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_042_0939</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666470">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666470</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267796</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_042_0939</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846044" alias="UCSF_VRP_mNGS_042_0940">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846044</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_042_0940</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666469">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666469</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267797</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_042_0940</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846045" alias="UCSF_VRP_mNGS_004_0095">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846045</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_004_0095</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666471">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666471</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266952</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_004_0095</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846046" alias="UCSF_VRP_mNGS_042_0941">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846046</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_042_0941</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666474">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666474</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267798</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_042_0941</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846047" alias="UCSF_VRP_mNGS_044_0986">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846047</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_044_0986</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666473">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666473</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267843</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_044_0986</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846048" alias="UCSF_VRP_mNGS_044_0987">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846048</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_044_0987</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666472">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666472</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267844</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_044_0987</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846049" alias="UCSF_VRP_mNGS_044_0988">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846049</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_044_0988</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666476">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666476</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267845</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_044_0988</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846050" alias="UCSF_VRP_mNGS_044_0989">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846050</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_044_0989</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666475">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666475</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267846</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_044_0989</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846051" alias="UCSF_VRP_mNGS_044_0990">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846051</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_044_0990</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666477">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666477</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267847</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_044_0990</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846052" alias="UCSF_VRP_mNGS_004_0100">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846052</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_004_0100</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666478">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666478</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266957</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_004_0100</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846053" alias="UCSF_VRP_mNGS_044_0991">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846053</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_044_0991</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666479">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666479</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267848</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_044_0991</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846054" alias="UCSF_VRP_mNGS_045_0992">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846054</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_045_0992</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666480">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666480</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267849</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_045_0992</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846055" alias="UCSF_VRP_mNGS_045_0993">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846055</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_045_0993</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666481">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666481</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267850</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_045_0993</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846056" alias="UCSF_VRP_mNGS_045_0994">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846056</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_045_0994</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666483">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666483</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267851</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_045_0994</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846057" alias="UCSF_VRP_mNGS_045_0995">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846057</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_045_0995</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666484">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666484</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267852</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_045_0995</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846058" alias="UCSF_VRP_mNGS_045_0996">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846058</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_045_0996</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666482">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666482</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267853</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_045_0996</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846059" alias="UCSF_VRP_mNGS_045_0997">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846059</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_045_0997</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666485">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666485</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267854</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_045_0997</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846060" alias="UCSF_VRP_mNGS_045_0998">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846060</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_045_0998</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666487">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666487</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267855</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_045_0998</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846061" alias="UCSF_VRP_mNGS_045_0999">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846061</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_045_0999</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666486">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666486</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267856</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_045_0999</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846062" alias="UCSF_VRP_mNGS_045_1000">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846062</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_045_1000</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666488">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666488</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267857</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_045_1000</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846063" alias="UCSF_VRP_mNGS_002_0039">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846063</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_002_0039</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666489">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666489</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266896</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_002_0039</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846064" alias="UCSF_VRP_mNGS_016_0381">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846064</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_016_0381</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666490">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666490</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267238</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_016_0381</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846065" alias="UCSF_VRP_mNGS_016_0382">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846065</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_016_0382</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666491">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666491</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267239</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_016_0382</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846066" alias="UCSF_VRP_mNGS_016_0383">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846066</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_016_0383</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666492">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666492</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267240</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_016_0383</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846067" alias="UCSF_VRP_mNGS_016_0384">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846067</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_016_0384</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666493">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666493</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267241</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_016_0384</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846068" alias="UCSF_VRP_mNGS_016_0385">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846068</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_016_0385</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666494">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666494</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267242</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_016_0385</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846069" alias="UCSF_VRP_mNGS_016_0386">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846069</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_016_0386</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666495">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666495</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267243</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_016_0386</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846070" alias="UCSF_VRP_mNGS_016_0387">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846070</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_016_0387</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666496">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666496</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267244</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_016_0387</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846071" alias="UCSF_VRP_mNGS_016_0388">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846071</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_016_0388</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666497">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666497</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267245</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_016_0388</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846072" alias="UCSF_VRP_mNGS_016_0389">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846072</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_016_0389</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666499">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666499</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267246</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_016_0389</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846073" alias="UCSF_VRP_mNGS_016_0390">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846073</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_016_0390</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666498">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666498</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267247</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_016_0390</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846074" alias="UCSF_VRP_mNGS_002_0040">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846074</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_002_0040</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666500">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666500</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266897</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_002_0040</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846075" alias="UCSF_VRP_mNGS_016_0391">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846075</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_016_0391</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666501">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666501</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267248</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_016_0391</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846076" alias="UCSF_VRP_mNGS_016_0392">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846076</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_016_0392</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666502">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666502</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267249</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_016_0392</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846077" alias="UCSF_VRP_mNGS_016_0393">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846077</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_016_0393</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666503">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666503</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267250</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_016_0393</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846078" alias="UCSF_VRP_mNGS_016_0394">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846078</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_016_0394</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666505">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666505</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267251</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_016_0394</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846079" alias="UCSF_VRP_mNGS_016_0395">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846079</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_016_0395</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666506">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666506</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267252</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_016_0395</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846080" alias="UCSF_VRP_mNGS_016_0396">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846080</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_016_0396</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666504">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666504</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267253</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_016_0396</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846081" alias="UCSF_VRP_mNGS_016_0397">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846081</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_016_0397</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666507">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666507</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267254</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_016_0397</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846082" alias="UCSF_VRP_mNGS_016_0398">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846082</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_016_0398</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666508">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666508</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267255</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_016_0398</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846083" alias="UCSF_VRP_mNGS_017_0399">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846083</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_017_0399</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666509">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666509</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267256</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_017_0399</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846084" alias="UCSF_VRP_mNGS_017_0400">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846084</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_017_0400</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666510">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666510</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267257</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_017_0400</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846085" alias="UCSF_VRP_mNGS_001_0005">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846085</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_001_0005</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666511">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666511</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266862</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_001_0005</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846086" alias="UCSF_VRP_mNGS_002_0041">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846086</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_002_0041</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666513">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666513</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266898</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_002_0041</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846087" alias="UCSF_VRP_mNGS_018_0445">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846087</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0445</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666512">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666512</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267302</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0445</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846088" alias="UCSF_VRP_mNGS_018_0446">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846088</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0446</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666514">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666514</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267303</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0446</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846089" alias="UCSF_VRP_mNGS_018_0447">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846089</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0447</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666516">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666516</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267304</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0447</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846090" alias="UCSF_VRP_mNGS_018_0448">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846090</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0448</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666515">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666515</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267305</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0448</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846091" alias="UCSF_VRP_mNGS_018_0449">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846091</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0449</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666517">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666517</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267306</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0449</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846092" alias="UCSF_VRP_mNGS_018_0450">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846092</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0450</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666518">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666518</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267307</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0450</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846093" alias="UCSF_VRP_mNGS_002_0046">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846093</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_002_0046</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666520">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666520</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266903</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_002_0046</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846094" alias="UCSF_VRP_mNGS_018_0451">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846094</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0451</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666521">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666521</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267308</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0451</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846095" alias="UCSF_VRP_mNGS_018_0452">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846095</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0452</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666519">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666519</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267309</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0452</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846096" alias="UCSF_VRP_mNGS_018_0453">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846096</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0453</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666522">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666522</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267310</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0453</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846097" alias="UCSF_VRP_mNGS_018_0454">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846097</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0454</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666523">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666523</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267311</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0454</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846098" alias="UCSF_VRP_mNGS_018_0455">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846098</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0455</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666524">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666524</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267312</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0455</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846099" alias="UCSF_VRP_mNGS_018_0456">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846099</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0456</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666525">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666525</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267313</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0456</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846100" alias="UCSF_VRP_mNGS_018_0457">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846100</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0457</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666526">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666526</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267314</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0457</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846101" alias="UCSF_VRP_mNGS_018_0458">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846101</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0458</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666528">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666528</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267315</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0458</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846102" alias="UCSF_VRP_mNGS_018_0459">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846102</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0459</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666529">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666529</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267316</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0459</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846103" alias="UCSF_VRP_mNGS_018_0460">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846103</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0460</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666527">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666527</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267317</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0460</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846104" alias="UCSF_VRP_mNGS_002_0047">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846104</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_002_0047</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666530">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666530</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266904</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_002_0047</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846105" alias="UCSF_VRP_mNGS_018_0461">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846105</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0461</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666532">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666532</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267318</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0461</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846106" alias="UCSF_VRP_mNGS_018_0462">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846106</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0462</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666531">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666531</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267319</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0462</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846107" alias="UCSF_VRP_mNGS_018_0463">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846107</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0463</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666533">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666533</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267320</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0463</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846108" alias="UCSF_VRP_mNGS_018_0464">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846108</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0464</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666534">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666534</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267321</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0464</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846109" alias="UCSF_VRP_mNGS_018_0465">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846109</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0465</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666535">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666535</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267322</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0465</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846110" alias="UCSF_VRP_mNGS_018_0466">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846110</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0466</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666536">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666536</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267323</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0466</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846111" alias="UCSF_VRP_mNGS_020_0510">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846111</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_020_0510</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666537">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666537</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267367</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_020_0510</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846112" alias="UCSF_VRP_mNGS_002_0052">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846112</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_002_0052</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666538">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666538</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266909</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_002_0052</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846113" alias="UCSF_VRP_mNGS_020_0511">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846113</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_020_0511</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666539">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666539</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267368</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_020_0511</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846114" alias="UCSF_VRP_mNGS_020_0512">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846114</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_020_0512</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666540">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666540</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267369</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_020_0512</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846115" alias="UCSF_VRP_mNGS_020_0513">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846115</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_020_0513</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666542">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666542</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267370</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_020_0513</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846116" alias="UCSF_VRP_mNGS_020_0514">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846116</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_020_0514</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666541">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666541</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267371</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_020_0514</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846117" alias="UCSF_VRP_mNGS_020_0515">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846117</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_020_0515</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666545">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666545</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267372</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_020_0515</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846118" alias="UCSF_VRP_mNGS_021_0516">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846118</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_021_0516</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666543">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666543</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267373</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_021_0516</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846119" alias="UCSF_VRP_mNGS_021_0517">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846119</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_021_0517</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666544">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666544</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267374</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_021_0517</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846120" alias="UCSF_VRP_mNGS_021_0518">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846120</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_021_0518</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666546">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666546</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267375</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_021_0518</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846121" alias="UCSF_VRP_mNGS_021_0519">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846121</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_021_0519</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666547">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666547</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267376</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_021_0519</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846122" alias="UCSF_VRP_mNGS_021_0520">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846122</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_021_0520</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666548">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666548</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267377</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_021_0520</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846123" alias="UCSF_VRP_mNGS_002_0053">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846123</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_002_0053</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666549">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666549</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266910</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_002_0053</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846124" alias="UCSF_VRP_mNGS_021_0521">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846124</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_021_0521</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666550">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666550</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267378</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_021_0521</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846125" alias="UCSF_VRP_mNGS_021_0522">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846125</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_021_0522</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666551">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666551</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267379</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_021_0522</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846126" alias="UCSF_VRP_mNGS_021_0523">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846126</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_021_0523</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666552">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666552</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267380</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_021_0523</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846127" alias="UCSF_VRP_mNGS_021_0524">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846127</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_021_0524</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666553">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666553</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267381</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_021_0524</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846128" alias="UCSF_VRP_mNGS_021_0525">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846128</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_021_0525</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666554">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666554</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267382</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_021_0525</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846129" alias="UCSF_VRP_mNGS_021_0526">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846129</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_021_0526</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666555">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666555</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267383</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_021_0526</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846130" alias="UCSF_VRP_mNGS_021_0527">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846130</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_021_0527</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666556">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666556</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267384</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_021_0527</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846131" alias="UCSF_VRP_mNGS_021_0528">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846131</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_021_0528</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666557">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666557</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267385</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_021_0528</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846132" alias="UCSF_VRP_mNGS_021_0529">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846132</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_021_0529</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666558">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666558</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267386</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_021_0529</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846133" alias="UCSF_VRP_mNGS_021_0530">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846133</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_021_0530</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666559">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666559</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267387</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_021_0530</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846134" alias="UCSF_VRP_mNGS_002_0054">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846134</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_002_0054</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666560">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666560</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266911</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_002_0054</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846135" alias="UCSF_VRP_mNGS_024_0575">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846135</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_024_0575</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666562">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666562</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267432</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_024_0575</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846136" alias="UCSF_VRP_mNGS_024_0576">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846136</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_024_0576</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666561">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666561</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267433</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_024_0576</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846137" alias="UCSF_VRP_mNGS_024_0577">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846137</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_024_0577</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666563">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666563</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267434</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_024_0577</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846138" alias="UCSF_VRP_mNGS_024_0578">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846138</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_024_0578</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666565">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666565</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267435</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_024_0578</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846139" alias="UCSF_VRP_mNGS_024_0579">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846139</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_024_0579</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666564">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666564</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267436</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_024_0579</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846140" alias="UCSF_VRP_mNGS_024_0580">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846140</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_024_0580</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666566">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666566</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267437</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_024_0580</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846141" alias="UCSF_VRP_mNGS_003_0059">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846141</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_003_0059</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666569">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666569</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266916</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_003_0059</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846142" alias="UCSF_VRP_mNGS_024_0581">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846142</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_024_0581</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666567">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666567</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267438</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_024_0581</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846143" alias="UCSF_VRP_mNGS_024_0582">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846143</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_024_0582</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666568">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666568</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267439</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_024_0582</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846144" alias="UCSF_VRP_mNGS_025_0583">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846144</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_025_0583</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666571">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666571</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267440</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_025_0583</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846145" alias="UCSF_VRP_mNGS_025_0584">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846145</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_025_0584</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666570">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666570</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267441</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_025_0584</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846146" alias="UCSF_VRP_mNGS_025_0585">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846146</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_025_0585</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666572">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666572</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267442</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_025_0585</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846147" alias="UCSF_VRP_mNGS_025_0586">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846147</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_025_0586</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666573">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666573</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267443</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_025_0586</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846148" alias="UCSF_VRP_mNGS_025_0587">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846148</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_025_0587</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666574">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666574</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267444</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_025_0587</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846149" alias="UCSF_VRP_mNGS_025_0588">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846149</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_025_0588</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666575">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666575</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267445</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_025_0588</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846150" alias="UCSF_VRP_mNGS_025_0589">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846150</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_025_0589</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666577">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666577</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267446</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_025_0589</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846151" alias="UCSF_VRP_mNGS_025_0590">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846151</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_025_0590</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666578">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666578</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267447</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_025_0590</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846152" alias="UCSF_VRP_mNGS_003_0060">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846152</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_003_0060</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666576">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666576</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266917</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_003_0060</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846153" alias="UCSF_VRP_mNGS_025_0591">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846153</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_025_0591</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666580">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666580</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267448</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_025_0591</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846154" alias="UCSF_VRP_mNGS_025_0592">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846154</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_025_0592</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666579">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666579</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267449</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_025_0592</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846155" alias="UCSF_VRP_mNGS_025_0593">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846155</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_025_0593</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666581">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666581</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267450</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_025_0593</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846156" alias="UCSF_VRP_mNGS_025_0594">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846156</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_025_0594</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666583">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666583</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267451</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_025_0594</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846157" alias="UCSF_VRP_mNGS_025_0595">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846157</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_025_0595</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666582">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666582</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267452</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_025_0595</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846158" alias="UCSF_VRP_mNGS_025_0596">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846158</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_025_0596</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666584">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666584</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267453</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_025_0596</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846159" alias="UCSF_VRP_mNGS_033_0748">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846159</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_033_0748</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666585">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666585</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267605</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_033_0748</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846160" alias="UCSF_VRP_mNGS_033_0749">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846160</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_033_0749</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666586">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666586</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267606</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_033_0749</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846161" alias="UCSF_VRP_mNGS_033_0750">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846161</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_033_0750</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666588">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666588</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267607</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_033_0750</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846162" alias="UCSF_VRP_mNGS_003_0076">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846162</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_003_0076</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666587">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666587</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266933</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_003_0076</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846163" alias="UCSF_VRP_mNGS_033_0751">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846163</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_033_0751</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666589">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666589</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267608</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_033_0751</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846164" alias="UCSF_VRP_mNGS_033_0752">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846164</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_033_0752</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666590">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666590</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267609</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_033_0752</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846165" alias="UCSF_VRP_mNGS_033_0753">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846165</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_033_0753</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666592">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666592</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267610</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_033_0753</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846166" alias="UCSF_VRP_mNGS_033_0754">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846166</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_033_0754</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666591">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666591</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267611</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_033_0754</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846167" alias="UCSF_VRP_mNGS_033_0755">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846167</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_033_0755</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666593">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666593</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267612</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_033_0755</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846168" alias="UCSF_VRP_mNGS_033_0756">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846168</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_033_0756</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666594">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666594</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267613</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_033_0756</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846169" alias="UCSF_VRP_mNGS_033_0757">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846169</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_033_0757</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666595">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666595</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267614</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_033_0757</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846170" alias="UCSF_VRP_mNGS_033_0758">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846170</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_033_0758</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666596">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666596</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267615</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_033_0758</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846171" alias="UCSF_VRP_mNGS_033_0759">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846171</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_033_0759</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666597">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666597</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267616</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_033_0759</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846172" alias="UCSF_VRP_mNGS_033_0760">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846172</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_033_0760</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666598">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666598</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267617</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_033_0760</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846173" alias="UCSF_VRP_mNGS_003_0077">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846173</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_003_0077</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666599">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666599</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266934</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_003_0077</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846174" alias="UCSF_VRP_mNGS_034_0761">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846174</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_034_0761</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666601">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666601</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267618</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_034_0761</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846175" alias="UCSF_VRP_mNGS_034_0762">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846175</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_034_0762</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666600">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666600</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267619</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_034_0762</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846176" alias="UCSF_VRP_mNGS_034_0763">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846176</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_034_0763</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666602">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666602</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267620</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_034_0763</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846177" alias="UCSF_VRP_mNGS_034_0764">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846177</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_034_0764</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666603">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666603</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267621</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_034_0764</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846178" alias="UCSF_VRP_mNGS_034_0765">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846178</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_034_0765</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666604">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666604</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267622</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_034_0765</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846179" alias="UCSF_VRP_mNGS_034_0766">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846179</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_034_0766</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666606">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666606</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267623</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_034_0766</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846180" alias="UCSF_VRP_mNGS_034_0767">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846180</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_034_0767</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666605">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666605</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267624</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_034_0767</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846181" alias="UCSF_VRP_mNGS_034_0768">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846181</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_034_0768</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666607">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666607</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267625</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_034_0768</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846182" alias="UCSF_VRP_mNGS_034_0769">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846182</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_034_0769</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666608">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666608</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267626</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_034_0769</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846183" alias="UCSF_VRP_mNGS_036_0812">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846183</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_036_0812</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666609">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666609</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267669</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_036_0812</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846184" alias="UCSF_VRP_mNGS_036_0813">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846184</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_036_0813</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666610">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666610</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267670</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_036_0813</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846185" alias="UCSF_VRP_mNGS_036_0814">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846185</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_036_0814</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666611">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666611</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267671</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_036_0814</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846186" alias="UCSF_VRP_mNGS_036_0815">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846186</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_036_0815</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666613">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666613</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267672</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_036_0815</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846187" alias="UCSF_VRP_mNGS_036_0816">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846187</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_036_0816</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666612">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666612</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267673</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_036_0816</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846188" alias="UCSF_VRP_mNGS_036_0817">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846188</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_036_0817</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666614">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666614</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267674</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_036_0817</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846189" alias="UCSF_VRP_mNGS_036_0818">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846189</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_036_0818</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666616">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666616</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267675</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_036_0818</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846190" alias="UCSF_VRP_mNGS_036_0819">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846190</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_036_0819</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666615">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666615</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267676</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_036_0819</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846191" alias="UCSF_VRP_mNGS_036_0820">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846191</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_036_0820</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666617">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666617</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267677</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_036_0820</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846192" alias="UCSF_VRP_mNGS_003_0083">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846192</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_003_0083</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666618">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666618</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266940</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_003_0083</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846193" alias="UCSF_VRP_mNGS_036_0821">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846193</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_036_0821</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666619">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666619</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267678</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_036_0821</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846194" alias="UCSF_VRP_mNGS_036_0822">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846194</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_036_0822</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666621">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666621</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267679</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_036_0822</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846195" alias="UCSF_VRP_mNGS_036_0823">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846195</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_036_0823</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666620">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666620</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267680</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_036_0823</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846196" alias="UCSF_VRP_mNGS_036_0824">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846196</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_036_0824</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666622">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666622</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267681</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_036_0824</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846197" alias="UCSF_VRP_mNGS_036_0825">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846197</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_036_0825</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666623">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666623</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267682</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_036_0825</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846198" alias="UCSF_VRP_mNGS_036_0826">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846198</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_036_0826</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666624">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666624</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267683</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_036_0826</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846199" alias="UCSF_VRP_mNGS_036_0827">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846199</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_036_0827</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666627">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666627</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267684</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_036_0827</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846200" alias="UCSF_VRP_mNGS_036_0828">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846200</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_036_0828</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666625">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666625</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267685</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_036_0828</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846201" alias="UCSF_VRP_mNGS_036_0829">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846201</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_036_0829</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666626">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666626</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267686</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_036_0829</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846202" alias="UCSF_VRP_mNGS_036_0830">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846202</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_036_0830</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666628">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666628</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267687</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_036_0830</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846203" alias="UCSF_VRP_mNGS_003_0084">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846203</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_003_0084</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666629">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666629</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266941</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_003_0084</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846204" alias="UCSF_VRP_mNGS_036_0831">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846204</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_036_0831</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666630">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666630</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267688</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_036_0831</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846205" alias="UCSF_VRP_mNGS_036_0832">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846205</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_036_0832</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666631">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666631</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267689</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_036_0832</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846206" alias="UCSF_VRP_mNGS_036_0833">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846206</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_036_0833</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666634">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666634</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267690</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_036_0833</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846207" alias="UCSF_VRP_mNGS_042_0942">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846207</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_042_0942</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666632">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666632</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267799</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_042_0942</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846208" alias="UCSF_VRP_mNGS_042_0943">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846208</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_042_0943</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666633">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666633</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267800</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_042_0943</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846209" alias="UCSF_VRP_mNGS_042_0944">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846209</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_042_0944</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666635">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666635</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267801</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_042_0944</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846210" alias="UCSF_VRP_mNGS_042_0945">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846210</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_042_0945</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666637">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666637</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267802</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_042_0945</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846211" alias="UCSF_VRP_mNGS_042_0946">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846211</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_042_0946</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666636">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666636</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267803</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_042_0946</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846212" alias="UCSF_VRP_mNGS_042_0947">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846212</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_042_0947</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666640">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666640</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267804</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_042_0947</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846213" alias="UCSF_VRP_mNGS_042_0948">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846213</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_042_0948</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666639">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666639</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267805</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_042_0948</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846214" alias="UCSF_VRP_mNGS_042_0949">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846214</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_042_0949</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666638">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666638</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267806</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_042_0949</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846215" alias="UCSF_VRP_mNGS_042_0950">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846215</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_042_0950</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666643">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666643</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267807</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_042_0950</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846216" alias="UCSF_VRP_mNGS_004_0096">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846216</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_004_0096</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666642">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666642</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266953</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_004_0096</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846217" alias="UCSF_VRP_mNGS_042_0951">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846217</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_042_0951</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666641">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666641</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267808</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_042_0951</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846218" alias="UCSF_VRP_mNGS_043_0952">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846218</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_043_0952</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666644">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666644</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267809</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_043_0952</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846219" alias="UCSF_VRP_mNGS_043_0953">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846219</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_043_0953</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666645">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666645</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267810</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_043_0953</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846220" alias="UCSF_VRP_mNGS_043_0954">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846220</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_043_0954</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666647">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666647</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267811</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_043_0954</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846221" alias="UCSF_VRP_mNGS_043_0955">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846221</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_043_0955</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666646">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666646</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267812</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_043_0955</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846222" alias="UCSF_VRP_mNGS_043_0956">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846222</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_043_0956</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666648">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666648</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267813</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_043_0956</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846223" alias="UCSF_VRP_mNGS_043_0957">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846223</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_043_0957</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666649">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666649</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267814</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_043_0957</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846224" alias="UCSF_VRP_mNGS_043_0958">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846224</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_043_0958</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666650">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666650</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267815</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_043_0958</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846225" alias="UCSF_VRP_mNGS_043_0959">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846225</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_043_0959</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666652">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666652</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267816</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_043_0959</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846226" alias="UCSF_VRP_mNGS_043_0960">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846226</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_043_0960</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666651">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666651</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267817</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_043_0960</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846227" alias="UCSF_VRP_mNGS_004_0097">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846227</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_004_0097</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666653">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666653</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266954</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_004_0097</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846228" alias="UCSF_VRP_mNGS_043_0961">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846228</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_043_0961</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666655">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666655</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267818</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_043_0961</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846229" alias="UCSF_VRP_mNGS_043_0962">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846229</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_043_0962</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666654">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666654</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267819</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_043_0962</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846230" alias="UCSF_VRP_mNGS_043_0963">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846230</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_043_0963</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666656">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666656</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267820</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_043_0963</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846231" alias="UCSF_VRP_mNGS_009_0186">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846231</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_009_0186</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666658">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666658</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267043</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_009_0186</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846232" alias="UCSF_VRP_mNGS_009_0187">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846232</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_009_0187</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666657">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666657</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267044</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_009_0187</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846233" alias="UCSF_VRP_mNGS_009_0188">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846233</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_009_0188</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666659">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666659</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267045</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_009_0188</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846234" alias="UCSF_VRP_mNGS_009_0189">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846234</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_009_0189</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666661">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666661</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267046</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_009_0189</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846235" alias="UCSF_VRP_mNGS_009_0190">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846235</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_009_0190</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666662">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666662</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267047</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_009_0190</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846236" alias="UCSF_VRP_mNGS_001_0020">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846236</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_001_0020</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666660">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666660</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266877</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_001_0020</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846237" alias="UCSF_VRP_mNGS_009_0191">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846237</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_009_0191</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666663">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666663</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267048</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_009_0191</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846238" alias="UCSF_VRP_mNGS_009_0192">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846238</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_009_0192</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666664">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666664</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267049</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_009_0192</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846239" alias="UCSF_VRP_mNGS_009_0193">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846239</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_009_0193</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666665">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666665</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267050</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_009_0193</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846240" alias="UCSF_VRP_mNGS_009_0194">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846240</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_009_0194</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666666">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666666</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267051</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_009_0194</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846241" alias="UCSF_VRP_mNGS_009_0195">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846241</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_009_0195</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666668">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666668</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267052</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_009_0195</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846242" alias="UCSF_VRP_mNGS_009_0196">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846242</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_009_0196</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666667">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666667</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267053</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_009_0196</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846243" alias="UCSF_VRP_mNGS_009_0197">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846243</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_009_0197</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666669">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666669</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267054</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_009_0197</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846244" alias="UCSF_VRP_mNGS_009_0198">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846244</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_009_0198</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666670">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666670</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267055</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_009_0198</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846245" alias="UCSF_VRP_mNGS_009_0199">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846245</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_009_0199</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666671">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666671</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267056</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_009_0199</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846246" alias="UCSF_VRP_mNGS_009_0200">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846246</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_009_0200</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666672">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666672</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267057</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_009_0200</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846247" alias="UCSF_VRP_mNGS_001_0003">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846247</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_001_0003</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666673">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666673</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266860</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_001_0003</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846248" alias="UCSF_VRP_mNGS_001_0021">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846248</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_001_0021</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666674">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666674</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266878</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_001_0021</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846249" alias="UCSF_VRP_mNGS_009_0201">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846249</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_009_0201</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666675">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666675</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267058</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_009_0201</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846250" alias="UCSF_VRP_mNGS_009_0202">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846250</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_009_0202</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666676">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666676</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267059</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_009_0202</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846251" alias="UCSF_VRP_mNGS_009_0203">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846251</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_009_0203</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666679">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666679</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267060</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_009_0203</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846252" alias="UCSF_VRP_mNGS_009_0204">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846252</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_009_0204</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666678">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666678</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267061</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_009_0204</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846253" alias="UCSF_VRP_mNGS_009_0205">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846253</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_009_0205</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666677">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666677</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267062</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_009_0205</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846254" alias="UCSF_VRP_mNGS_009_0206">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846254</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_009_0206</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666680">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666680</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267063</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_009_0206</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846255" alias="UCSF_VRP_mNGS_001_0026">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846255</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_001_0026</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666681">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666681</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266883</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_001_0026</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846256" alias="UCSF_VRP_mNGS_011_0251">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846256</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_011_0251</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666682">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666682</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267108</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_011_0251</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846257" alias="UCSF_VRP_mNGS_011_0252">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846257</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_011_0252</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666683">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666683</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267109</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_011_0252</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846258" alias="UCSF_VRP_mNGS_011_0253">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846258</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_011_0253</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666684">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666684</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267110</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_011_0253</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846259" alias="UCSF_VRP_mNGS_011_0254">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846259</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_011_0254</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666686">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666686</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267111</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_011_0254</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846260" alias="UCSF_VRP_mNGS_011_0255">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846260</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_011_0255</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666685">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666685</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267112</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_011_0255</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846261" alias="UCSF_VRP_mNGS_011_0256">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846261</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_011_0256</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666687">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666687</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267113</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_011_0256</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846262" alias="UCSF_VRP_mNGS_011_0257">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846262</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_011_0257</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666688">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666688</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267114</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_011_0257</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846263" alias="UCSF_VRP_mNGS_011_0258">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846263</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_011_0258</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666689">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666689</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267115</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_011_0258</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846264" alias="UCSF_VRP_mNGS_012_0259">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846264</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_012_0259</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666690">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666690</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267116</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_012_0259</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846265" alias="UCSF_VRP_mNGS_012_0260">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846265</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_012_0260</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666691">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666691</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267117</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_012_0260</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846266" alias="UCSF_VRP_mNGS_001_0027">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846266</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_001_0027</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666692">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666692</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266884</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_001_0027</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846267" alias="UCSF_VRP_mNGS_012_0261">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846267</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_012_0261</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666693">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666693</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267118</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_012_0261</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846268" alias="UCSF_VRP_mNGS_012_0262">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846268</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_012_0262</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666694">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666694</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267119</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_012_0262</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846269" alias="UCSF_VRP_mNGS_012_0263">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846269</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_012_0263</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666695">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666695</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267120</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_012_0263</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846270" alias="UCSF_VRP_mNGS_012_0264">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846270</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_012_0264</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666697">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666697</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267121</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_012_0264</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846271" alias="UCSF_VRP_mNGS_012_0265">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846271</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_012_0265</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666696">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666696</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267122</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_012_0265</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846272" alias="UCSF_VRP_mNGS_012_0266">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846272</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_012_0266</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666698">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666698</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267123</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_012_0266</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846273" alias="UCSF_VRP_mNGS_012_0267">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846273</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_012_0267</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666702">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666702</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267124</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_012_0267</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846274" alias="UCSF_VRP_mNGS_012_0268">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846274</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_012_0268</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666700">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666700</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267125</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_012_0268</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846275" alias="UCSF_VRP_mNGS_012_0269">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846275</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_012_0269</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666699">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666699</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267126</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_012_0269</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846276" alias="UCSF_VRP_mNGS_012_0270">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846276</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_012_0270</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666701">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666701</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267127</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_012_0270</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846277" alias="UCSF_VRP_mNGS_001_0028">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846277</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_001_0028</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666703">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666703</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266885</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_001_0028</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846278" alias="UCSF_VRP_mNGS_012_0271">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846278</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_012_0271</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666705">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666705</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267128</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_012_0271</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846279" alias="UCSF_VRP_mNGS_001_0001">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846279</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_001_0001</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666704">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666704</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266858</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_001_0001</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846280" alias="UCSF_VRP_mNGS_001_0002">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846280</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_001_0002</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666706">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666706</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266859</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_001_0002</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846281" alias="UCSF_VRP_mNGS_001_0011">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846281</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_001_0011</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666707">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666707</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266868</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_001_0011</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846282" alias="UCSF_VRP_mNGS_004_0101">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846282</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_004_0101</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666709">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666709</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266958</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_004_0101</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846283" alias="UCSF_VRP_mNGS_004_0102">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846283</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_004_0102</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666708">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666708</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266959</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_004_0102</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846284" alias="UCSF_VRP_mNGS_004_0103">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846284</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_004_0103</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666710">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666710</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266960</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_004_0103</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846285" alias="UCSF_VRP_mNGS_004_0104">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846285</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_004_0104</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666711">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666711</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266961</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_004_0104</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846286" alias="UCSF_VRP_mNGS_004_0105">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846286</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_004_0105</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666712">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666712</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266962</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_004_0105</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846287" alias="UCSF_VRP_mNGS_004_0106">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846287</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_004_0106</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666713">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666713</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266963</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_004_0106</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846288" alias="UCSF_VRP_mNGS_004_0107">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846288</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_004_0107</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666715">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666715</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266964</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_004_0107</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846289" alias="UCSF_VRP_mNGS_004_0108">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846289</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_004_0108</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666714">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666714</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266965</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_004_0108</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846290" alias="UCSF_VRP_mNGS_004_0109">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846290</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_004_0109</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666716">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666716</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266966</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_004_0109</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846291" alias="UCSF_VRP_mNGS_004_0110">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846291</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_004_0110</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666717">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666717</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266967</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_004_0110</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846292" alias="UCSF_VRP_mNGS_001_0012">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846292</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_001_0012</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666718">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666718</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266869</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_001_0012</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846293" alias="UCSF_VRP_mNGS_004_0111">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846293</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_004_0111</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666719">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666719</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266968</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_004_0111</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846294" alias="UCSF_VRP_mNGS_004_0112">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846294</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_004_0112</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666722">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666722</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266969</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_004_0112</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846295" alias="UCSF_VRP_mNGS_004_0113">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846295</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_004_0113</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666723">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666723</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266970</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_004_0113</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846296" alias="UCSF_VRP_mNGS_004_0114">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846296</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_004_0114</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666720">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666720</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266971</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_004_0114</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846297" alias="UCSF_VRP_mNGS_004_0115">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846297</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_004_0115</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666721">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666721</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266972</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_004_0115</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846298" alias="UCSF_VRP_mNGS_004_0116">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846298</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_004_0116</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666726">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666726</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266973</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_004_0116</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846299" alias="UCSF_VRP_mNGS_004_0117">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846299</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_004_0117</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666727">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666727</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266974</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_004_0117</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846300" alias="UCSF_VRP_mNGS_004_0118">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846300</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_004_0118</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666724">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666724</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266975</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_004_0118</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846301" alias="UCSF_VRP_mNGS_004_0119">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846301</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_004_0119</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666725">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666725</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266976</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_004_0119</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846302" alias="UCSF_VRP_mNGS_004_0120">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846302</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_004_0120</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666728">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666728</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266977</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_004_0120</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846303" alias="UCSF_VRP_mNGS_001_0013">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846303</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_001_0013</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666731">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666731</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266870</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_001_0013</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846304" alias="UCSF_VRP_mNGS_004_0121">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846304</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_004_0121</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666730">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666730</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266978</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_004_0121</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846305" alias="UCSF_VRP_mNGS_004_0122">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846305</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_004_0122</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666729">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666729</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266979</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_004_0122</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846306" alias="UCSF_VRP_mNGS_004_0123">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846306</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_004_0123</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666732">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666732</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266980</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_004_0123</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846307" alias="UCSF_VRP_mNGS_004_0124">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846307</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_004_0124</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666733">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666733</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266981</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_004_0124</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846308" alias="UCSF_VRP_mNGS_004_0125">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846308</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_004_0125</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666734">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666734</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266982</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_004_0125</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846309" alias="UCSF_VRP_mNGS_004_0126">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846309</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_004_0126</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666735">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666735</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266983</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_004_0126</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846310" alias="UCSF_VRP_mNGS_004_0127">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846310</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_004_0127</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666736">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666736</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266984</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_004_0127</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846311" alias="UCSF_VRP_mNGS_004_0128">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846311</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_004_0128</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666737">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666737</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266985</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_004_0128</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846312" alias="UCSF_VRP_mNGS_005_0129">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846312</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_005_0129</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666738">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666738</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266986</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_005_0129</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846313" alias="UCSF_VRP_mNGS_005_0130">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846313</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_005_0130</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666739">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666739</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266987</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_005_0130</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846314" alias="UCSF_VRP_mNGS_001_0014">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846314</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_001_0014</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666741">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666741</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266871</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_001_0014</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846315" alias="UCSF_VRP_mNGS_005_0131">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846315</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_005_0131</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666740">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666740</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266988</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_005_0131</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846316" alias="UCSF_VRP_mNGS_005_0132">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846316</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_005_0132</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666742">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666742</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266989</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_005_0132</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846317" alias="UCSF_VRP_mNGS_005_0133">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846317</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_005_0133</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666743">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666743</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266990</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_005_0133</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846318" alias="UCSF_VRP_mNGS_005_0134">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846318</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_005_0134</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666744">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666744</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266991</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_005_0134</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846319" alias="UCSF_VRP_mNGS_005_0135">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846319</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_005_0135</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666746">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666746</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266992</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_005_0135</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846320" alias="UCSF_VRP_mNGS_005_0136">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846320</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_005_0136</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666747">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666747</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266993</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_005_0136</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846321" alias="UCSF_VRP_mNGS_005_0137">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846321</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_005_0137</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666745">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666745</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266994</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_005_0137</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846322" alias="UCSF_VRP_mNGS_005_0138">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846322</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_005_0138</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666748">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666748</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266995</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_005_0138</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846323" alias="UCSF_VRP_mNGS_005_0139">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846323</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_005_0139</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666749">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666749</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266996</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_005_0139</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846324" alias="UCSF_VRP_mNGS_005_0140">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846324</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_005_0140</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666751">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666751</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266997</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_005_0140</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846325" alias="UCSF_VRP_mNGS_001_0015">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846325</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_001_0015</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666750">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666750</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266872</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_001_0015</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846326" alias="UCSF_VRP_mNGS_006_0141">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846326</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_006_0141</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666752">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666752</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266998</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_006_0141</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiniSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846327" alias="UCSF_VRP_mNGS_009_0207">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846327</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_009_0207</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666753">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666753</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267064</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_009_0207</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846328" alias="UCSF_VRP_mNGS_009_0208">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846328</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_009_0208</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666754">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666754</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267065</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_009_0208</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846329" alias="UCSF_VRP_mNGS_009_0209">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846329</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_009_0209</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666756">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666756</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267066</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_009_0209</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846330" alias="UCSF_VRP_mNGS_009_0210">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846330</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_009_0210</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666755">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666755</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267067</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_009_0210</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846331" alias="UCSF_VRP_mNGS_001_0022">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846331</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_001_0022</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666757">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666757</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266879</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_001_0022</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846332" alias="UCSF_VRP_mNGS_010_0211">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846332</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_010_0211</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666759">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666759</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267068</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_010_0211</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846333" alias="UCSF_VRP_mNGS_010_0212">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846333</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_010_0212</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666758">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666758</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267069</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_010_0212</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846334" alias="UCSF_VRP_mNGS_010_0213">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846334</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_010_0213</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666761">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666761</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267070</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_010_0213</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846335" alias="UCSF_VRP_mNGS_010_0214">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846335</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_010_0214</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666762">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666762</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267071</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_010_0214</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846336" alias="UCSF_VRP_mNGS_010_0215">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846336</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_010_0215</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666760">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666760</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267072</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_010_0215</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846337" alias="UCSF_VRP_mNGS_010_0216">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846337</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_010_0216</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666764">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666764</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267073</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_010_0216</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846338" alias="UCSF_VRP_mNGS_010_0217">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846338</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_010_0217</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666763">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666763</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267074</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_010_0217</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846339" alias="UCSF_VRP_mNGS_010_0218">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846339</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_010_0218</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666766">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666766</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267075</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_010_0218</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846340" alias="UCSF_VRP_mNGS_010_0219">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846340</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_010_0219</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666765">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666765</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267076</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_010_0219</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846341" alias="UCSF_VRP_mNGS_010_0220">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846341</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_010_0220</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666767">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666767</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267077</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_010_0220</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846342" alias="UCSF_VRP_mNGS_001_0023">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846342</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_001_0023</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666768">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666768</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266880</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_001_0023</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846343" alias="UCSF_VRP_mNGS_010_0221">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846343</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_010_0221</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666769">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666769</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267078</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_010_0221</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846344" alias="UCSF_VRP_mNGS_010_0222">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846344</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_010_0222</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666770">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666770</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267079</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_010_0222</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846345" alias="UCSF_VRP_mNGS_010_0223">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846345</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_010_0223</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666771">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666771</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267080</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_010_0223</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846346" alias="UCSF_VRP_mNGS_010_0224">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846346</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_010_0224</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666772">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666772</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267081</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_010_0224</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846347" alias="UCSF_VRP_mNGS_010_0225">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846347</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_010_0225</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666773">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666773</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267082</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_010_0225</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846348" alias="UCSF_VRP_mNGS_010_0226">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846348</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_010_0226</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666774">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666774</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267083</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_010_0226</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846349" alias="UCSF_VRP_mNGS_011_0227">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846349</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_011_0227</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666776">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666776</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267084</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_011_0227</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846350" alias="UCSF_VRP_mNGS_011_0228">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846350</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_011_0228</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666775">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666775</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267085</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_011_0228</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846351" alias="UCSF_VRP_mNGS_012_0272">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846351</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_012_0272</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666777">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666777</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267129</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_012_0272</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846352" alias="UCSF_VRP_mNGS_012_0273">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846352</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_012_0273</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666779">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666779</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267130</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_012_0273</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846353" alias="UCSF_VRP_mNGS_012_0274">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846353</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_012_0274</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666781">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666781</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267131</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_012_0274</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846354" alias="UCSF_VRP_mNGS_012_0275">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846354</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_012_0275</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666778">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666778</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267132</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_012_0275</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846355" alias="UCSF_VRP_mNGS_012_0276">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846355</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_012_0276</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666782">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666782</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267133</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_012_0276</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846356" alias="UCSF_VRP_mNGS_012_0277">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846356</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_012_0277</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666780">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666780</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267134</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_012_0277</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846357" alias="UCSF_VRP_mNGS_012_0278">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846357</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_012_0278</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666783">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666783</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267135</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_012_0278</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846358" alias="UCSF_VRP_mNGS_012_0279">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846358</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_012_0279</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666784">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666784</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267136</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_012_0279</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846359" alias="UCSF_VRP_mNGS_012_0280">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846359</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_012_0280</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666785">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666785</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267137</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_012_0280</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846360" alias="UCSF_VRP_mNGS_001_0029">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846360</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_001_0029</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666786">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666786</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266886</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_001_0029</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846361" alias="UCSF_VRP_mNGS_012_0281">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846361</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_012_0281</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666790">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666790</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267138</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_012_0281</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846362" alias="UCSF_VRP_mNGS_012_0282">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846362</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_012_0282</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666787">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666787</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267139</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_012_0282</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846363" alias="UCSF_VRP_mNGS_012_0283">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846363</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_012_0283</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666789">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666789</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267140</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_012_0283</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846364" alias="UCSF_VRP_mNGS_012_0284">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846364</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_012_0284</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666788">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666788</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267141</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_012_0284</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846365" alias="UCSF_VRP_mNGS_012_0285">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846365</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_012_0285</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666792">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666792</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267142</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_012_0285</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846366" alias="UCSF_VRP_mNGS_012_0286">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846366</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_012_0286</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666791">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666791</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267143</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_012_0286</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846367" alias="UCSF_VRP_mNGS_013_0287">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846367</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_013_0287</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666793">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666793</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267144</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_013_0287</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846368" alias="UCSF_VRP_mNGS_013_0288">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846368</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_013_0288</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666794">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666794</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267145</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_013_0288</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846369" alias="UCSF_VRP_mNGS_013_0289">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846369</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_013_0289</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666795">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666795</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267146</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_013_0289</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846370" alias="UCSF_VRP_mNGS_013_0290">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846370</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_013_0290</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666796">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666796</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267147</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_013_0290</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846371" alias="UCSF_VRP_mNGS_001_0030">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846371</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_001_0030</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666797">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266887</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_001_0030</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846372" alias="UCSF_VRP_mNGS_013_0291">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846372</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_013_0291</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666799">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666799</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267148</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_013_0291</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846373" alias="UCSF_VRP_mNGS_013_0292">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846373</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_013_0292</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666801">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666801</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267149</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_013_0292</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846374" alias="UCSF_VRP_mNGS_013_0293">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846374</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_013_0293</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666800">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666800</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267150</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_013_0293</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846375" alias="UCSF_VRP_mNGS_014_0337">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846375</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_014_0337</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666798">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666798</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267194</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_014_0337</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846376" alias="UCSF_VRP_mNGS_014_0338">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846376</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_014_0338</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666804">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666804</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267195</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_014_0338</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846377" alias="UCSF_VRP_mNGS_014_0339">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846377</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_014_0339</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666805">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666805</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267196</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_014_0339</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846378" alias="UCSF_VRP_mNGS_014_0340">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846378</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_014_0340</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666802">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666802</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267197</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_014_0340</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846379" alias="UCSF_VRP_mNGS_002_0035">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846379</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_002_0035</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666807">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666807</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266892</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_002_0035</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846380" alias="UCSF_VRP_mNGS_014_0341">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846380</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_014_0341</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666806">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666806</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267198</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_014_0341</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846381" alias="UCSF_VRP_mNGS_014_0342">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846381</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_014_0342</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666803">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666803</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267199</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_014_0342</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846382" alias="UCSF_VRP_mNGS_015_0343">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846382</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_015_0343</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666809">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666809</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267200</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_015_0343</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846383" alias="UCSF_VRP_mNGS_015_0344">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846383</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_015_0344</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666808">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666808</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267201</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_015_0344</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846384" alias="UCSF_VRP_mNGS_015_0345">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846384</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_015_0345</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666810">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666810</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267202</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_015_0345</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846385" alias="UCSF_VRP_mNGS_015_0346">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846385</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_015_0346</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666812">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666812</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267203</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_015_0346</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846386" alias="UCSF_VRP_mNGS_015_0347">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846386</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_015_0347</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666811">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666811</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267204</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_015_0347</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846387" alias="UCSF_VRP_mNGS_015_0348">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846387</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_015_0348</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666814">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666814</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267205</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_015_0348</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846388" alias="UCSF_VRP_mNGS_015_0349">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846388</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_015_0349</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666813">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666813</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267206</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_015_0349</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846389" alias="UCSF_VRP_mNGS_015_0350">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846389</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_015_0350</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666815">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666815</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267207</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_015_0350</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846390" alias="UCSF_VRP_mNGS_002_0036">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846390</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_002_0036</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666817">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666817</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266893</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_002_0036</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846391" alias="UCSF_VRP_mNGS_015_0351">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846391</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_015_0351</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666816">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666816</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267208</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_015_0351</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846392" alias="UCSF_VRP_mNGS_015_0352">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846392</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_015_0352</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666818">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666818</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267209</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_015_0352</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846393" alias="UCSF_VRP_mNGS_015_0353">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846393</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_015_0353</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666819">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666819</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267210</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_015_0353</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846394" alias="UCSF_VRP_mNGS_015_0354">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846394</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_015_0354</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666820">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666820</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267211</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_015_0354</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846395" alias="UCSF_VRP_mNGS_015_0355">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846395</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_015_0355</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666821">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666821</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267212</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_015_0355</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846396" alias="UCSF_VRP_mNGS_015_0356">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846396</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_015_0356</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666822">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666822</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267213</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_015_0356</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846397" alias="UCSF_VRP_mNGS_015_0357">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846397</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_015_0357</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666823">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666823</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267214</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_015_0357</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846398" alias="UCSF_VRP_mNGS_015_0358">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846398</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_015_0358</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666824">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666824</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267215</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_015_0358</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846399" alias="UCSF_VRP_mNGS_017_0401">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846399</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_017_0401</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666826">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666826</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267258</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_017_0401</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846400" alias="UCSF_VRP_mNGS_017_0402">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846400</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_017_0402</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666825">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666825</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267259</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_017_0402</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846401" alias="UCSF_VRP_mNGS_017_0403">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846401</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_017_0403</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666828">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666828</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267260</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_017_0403</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846402" alias="UCSF_VRP_mNGS_017_0404">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846402</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_017_0404</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666827">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666827</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267261</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_017_0404</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846403" alias="UCSF_VRP_mNGS_017_0405">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846403</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_017_0405</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666829">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666829</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267262</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_017_0405</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846404" alias="UCSF_VRP_mNGS_017_0406">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846404</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_017_0406</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666830">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666830</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267263</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_017_0406</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846405" alias="UCSF_VRP_mNGS_017_0407">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846405</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_017_0407</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666831">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666831</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267264</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_017_0407</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846406" alias="UCSF_VRP_mNGS_017_0408">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846406</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_017_0408</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666833">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666833</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267265</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_017_0408</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846407" alias="UCSF_VRP_mNGS_017_0409">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846407</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_017_0409</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666832">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666832</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267266</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_017_0409</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846408" alias="UCSF_VRP_mNGS_017_0410">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846408</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_017_0410</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666834">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666834</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267267</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_017_0410</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846409" alias="UCSF_VRP_mNGS_002_0042">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846409</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_002_0042</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666835">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666835</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266899</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_002_0042</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846410" alias="UCSF_VRP_mNGS_017_0411">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846410</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_017_0411</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666836">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666836</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267268</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_017_0411</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846411" alias="UCSF_VRP_mNGS_017_0412">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846411</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_017_0412</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666837">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666837</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267269</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_017_0412</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846412" alias="UCSF_VRP_mNGS_017_0413">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846412</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_017_0413</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666838">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666838</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267270</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_017_0413</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846413" alias="UCSF_VRP_mNGS_017_0414">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846413</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_017_0414</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666839">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666839</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267271</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_017_0414</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846414" alias="UCSF_VRP_mNGS_017_0415">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846414</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_017_0415</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666841">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666841</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267272</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_017_0415</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846415" alias="UCSF_VRP_mNGS_017_0416">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846415</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_017_0416</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666843">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666843</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267273</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_017_0416</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846416" alias="UCSF_VRP_mNGS_017_0417">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846416</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_017_0417</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666842">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666842</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267274</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_017_0417</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846417" alias="UCSF_VRP_mNGS_017_0418">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846417</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_017_0418</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666840">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666840</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267275</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_017_0418</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846418" alias="UCSF_VRP_mNGS_017_0419">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846418</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_017_0419</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666844">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666844</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267276</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_017_0419</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846419" alias="UCSF_VRP_mNGS_017_0420">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846419</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_017_0420</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666845">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666845</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267277</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_017_0420</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846420" alias="UCSF_VRP_mNGS_002_0043">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846420</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_002_0043</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666846">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666846</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266900</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_002_0043</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846421" alias="UCSF_VRP_mNGS_017_0421">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846421</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_017_0421</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666848">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666848</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267278</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_017_0421</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846422" alias="UCSF_VRP_mNGS_017_0422">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846422</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_017_0422</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666850">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666850</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267279</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_017_0422</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846423" alias="UCSF_VRP_mNGS_018_0467">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846423</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0467</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666847">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666847</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267324</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0467</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846424" alias="UCSF_VRP_mNGS_018_0468">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846424</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0468</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666849">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666849</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267325</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0468</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846425" alias="UCSF_VRP_mNGS_018_0469">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846425</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0469</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666851">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666851</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267326</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0469</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846426" alias="UCSF_VRP_mNGS_018_0470">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846426</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0470</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666855">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666855</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267327</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0470</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846427" alias="UCSF_VRP_mNGS_002_0048">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846427</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_002_0048</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666852">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666852</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266905</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_002_0048</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846428" alias="UCSF_VRP_mNGS_018_0471">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846428</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0471</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666853">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666853</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267328</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0471</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846429" alias="UCSF_VRP_mNGS_018_0472">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846429</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0472</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666854">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666854</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267329</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0472</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846430" alias="UCSF_VRP_mNGS_018_0473">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846430</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0473</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666856">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666856</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267330</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0473</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846431" alias="UCSF_VRP_mNGS_018_0474">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846431</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0474</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666857">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666857</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267331</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0474</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846432" alias="UCSF_VRP_mNGS_018_0475">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846432</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0475</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666858">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666858</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267332</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0475</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846433" alias="UCSF_VRP_mNGS_018_0476">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846433</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0476</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666861">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666861</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267333</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0476</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846434" alias="UCSF_VRP_mNGS_018_0477">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846434</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0477</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666862">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666862</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267334</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0477</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846435" alias="UCSF_VRP_mNGS_018_0478">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846435</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0478</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666859">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666859</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267335</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0478</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846436" alias="UCSF_VRP_mNGS_018_0479">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846436</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0479</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666860">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666860</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267336</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0479</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846437" alias="UCSF_VRP_mNGS_018_0480">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846437</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0480</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666863">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666863</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267337</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0480</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846438" alias="UCSF_VRP_mNGS_002_0049">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846438</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_002_0049</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666864">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666864</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266906</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_002_0049</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846439" alias="UCSF_VRP_mNGS_018_0481">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846439</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0481</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666866">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666866</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267338</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0481</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846440" alias="UCSF_VRP_mNGS_018_0482">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846440</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0482</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666865">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666865</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267339</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0482</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846441" alias="UCSF_VRP_mNGS_018_0483">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846441</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0483</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666868">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666868</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267340</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0483</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846442" alias="UCSF_VRP_mNGS_018_0484">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846442</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0484</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666867">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666867</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267341</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0484</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846443" alias="UCSF_VRP_mNGS_018_0485">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846443</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_018_0485</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666869">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666869</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267342</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_018_0485</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846444" alias="UCSF_VRP_mNGS_019_0486">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846444</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_019_0486</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666870">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666870</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267343</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_019_0486</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846445" alias="UCSF_VRP_mNGS_019_0487">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846445</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_019_0487</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666876">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666876</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267344</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_019_0487</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846446" alias="UCSF_VRP_mNGS_019_0488">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846446</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_019_0488</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666871">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666871</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267345</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_019_0488</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846447" alias="UCSF_VRP_mNGS_021_0531">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846447</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_021_0531</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666872">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666872</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267388</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_021_0531</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846448" alias="UCSF_VRP_mNGS_021_0532">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846448</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_021_0532</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666874">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666874</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267389</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_021_0532</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846449" alias="UCSF_VRP_mNGS_021_0533">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846449</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_021_0533</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666875">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666875</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267390</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_021_0533</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846450" alias="UCSF_VRP_mNGS_021_0534">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846450</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_021_0534</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666873">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666873</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267391</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_021_0534</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846451" alias="UCSF_VRP_mNGS_022_0535">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846451</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_022_0535</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666877">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666877</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267392</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_022_0535</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846452" alias="UCSF_VRP_mNGS_022_0536">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846452</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_022_0536</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666879">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666879</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267393</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_022_0536</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846453" alias="UCSF_VRP_mNGS_022_0537">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846453</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_022_0537</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666878">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666878</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267394</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_022_0537</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846454" alias="UCSF_VRP_mNGS_022_0538">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846454</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_022_0538</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666880">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666880</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267395</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_022_0538</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846455" alias="UCSF_VRP_mNGS_022_0539">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846455</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_022_0539</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666881">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666881</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267396</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_022_0539</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846456" alias="UCSF_VRP_mNGS_022_0540">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846456</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_022_0540</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666882">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666882</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267397</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_022_0540</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846457" alias="UCSF_VRP_mNGS_003_0055">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846457</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_003_0055</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666883">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666883</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266912</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_003_0055</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846458" alias="UCSF_VRP_mNGS_022_0541">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846458</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_022_0541</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666884">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666884</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267398</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_022_0541</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846459" alias="UCSF_VRP_mNGS_022_0542">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846459</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_022_0542</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666888">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666888</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267399</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_022_0542</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846460" alias="UCSF_VRP_mNGS_022_0543">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846460</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_022_0543</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666886">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666886</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267400</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_022_0543</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846461" alias="UCSF_VRP_mNGS_022_0544">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846461</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_022_0544</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666885">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666885</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267401</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_022_0544</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846462" alias="UCSF_VRP_mNGS_022_0545">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846462</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_022_0545</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666887">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666887</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267402</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_022_0545</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846463" alias="UCSF_VRP_mNGS_022_0546">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846463</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_022_0546</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666889">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666889</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267403</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_022_0546</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846464" alias="UCSF_VRP_mNGS_022_0547">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846464</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_022_0547</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666890">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666890</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267404</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_022_0547</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846465" alias="UCSF_VRP_mNGS_022_0548">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846465</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_022_0548</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666891">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666891</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267405</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_022_0548</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846466" alias="UCSF_VRP_mNGS_022_0549">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846466</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_022_0549</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666893">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666893</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267406</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_022_0549</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846467" alias="UCSF_VRP_mNGS_023_0550">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846467</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_023_0550</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666892">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666892</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267407</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_023_0550</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846468" alias="UCSF_VRP_mNGS_003_0056">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846468</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_003_0056</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666894">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666894</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266913</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_003_0056</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846469" alias="UCSF_VRP_mNGS_023_0551">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846469</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_023_0551</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666897">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666897</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267408</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_023_0551</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846470" alias="UCSF_VRP_mNGS_023_0552">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846470</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_023_0552</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666895">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666895</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267409</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_023_0552</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846471" alias="UCSF_VRP_mNGS_025_0597">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846471</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_025_0597</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666896">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666896</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267454</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_025_0597</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846472" alias="UCSF_VRP_mNGS_025_0598">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846472</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_025_0598</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666899">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666899</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267455</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_025_0598</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846473" alias="UCSF_VRP_mNGS_025_0599">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846473</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_025_0599</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666898">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666898</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267456</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_025_0599</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846474" alias="UCSF_VRP_mNGS_025_0600">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846474</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_025_0600</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666900">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666900</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267457</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_025_0600</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846475" alias="UCSF_VRP_mNGS_001_0007">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846475</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_001_0007</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666901">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666901</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266864</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_001_0007</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846476" alias="UCSF_VRP_mNGS_003_0061">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846476</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_003_0061</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666902">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666902</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266918</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_003_0061</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846477" alias="UCSF_VRP_mNGS_025_0601">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846477</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_025_0601</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666904">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666904</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267458</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_025_0601</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846478" alias="UCSF_VRP_mNGS_026_0602">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846478</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_026_0602</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666903">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666903</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267459</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_026_0602</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846479" alias="UCSF_VRP_mNGS_026_0603">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846479</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_026_0603</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666907">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666907</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267460</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_026_0603</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846480" alias="UCSF_VRP_mNGS_026_0604">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846480</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_026_0604</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666906">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666906</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267461</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_026_0604</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846481" alias="UCSF_VRP_mNGS_026_0605">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846481</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_026_0605</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666908">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666908</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267462</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_026_0605</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846482" alias="UCSF_VRP_mNGS_026_0606">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846482</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_026_0606</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666905">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666905</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267463</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_026_0606</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846483" alias="UCSF_VRP_mNGS_026_0607">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846483</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_026_0607</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666909">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666909</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267464</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_026_0607</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846484" alias="UCSF_VRP_mNGS_026_0608">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846484</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_026_0608</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666912">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666912</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267465</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_026_0608</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846485" alias="UCSF_VRP_mNGS_026_0609">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846485</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_026_0609</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666911">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666911</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267466</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_026_0609</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846486" alias="UCSF_VRP_mNGS_026_0610">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846486</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_026_0610</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666910">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666910</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267467</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_026_0610</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846487" alias="UCSF_VRP_mNGS_003_0062">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846487</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_003_0062</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666914">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666914</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266919</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_003_0062</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846488" alias="UCSF_VRP_mNGS_026_0611">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846488</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_026_0611</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666913">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666913</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267468</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_026_0611</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846489" alias="UCSF_VRP_mNGS_026_0612">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846489</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_026_0612</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666915">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666915</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267469</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_026_0612</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846490" alias="UCSF_VRP_mNGS_026_0613">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846490</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_026_0613</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666916">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666916</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267470</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_026_0613</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846491" alias="UCSF_VRP_mNGS_026_0614">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846491</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_026_0614</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666918">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666918</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267471</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_026_0614</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846492" alias="UCSF_VRP_mNGS_026_0615">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846492</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_026_0615</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666919">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666919</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267472</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_026_0615</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846493" alias="UCSF_VRP_mNGS_026_0616">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846493</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_026_0616</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666917">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666917</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267473</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_026_0616</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846494" alias="UCSF_VRP_mNGS_026_0617">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846494</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_026_0617</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666920">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666920</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267474</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_026_0617</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846495" alias="UCSF_VRP_mNGS_027_0640">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846495</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_027_0640</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666924">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666924</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267497</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_027_0640</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846496" alias="UCSF_VRP_mNGS_003_0065">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846496</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_003_0065</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666921">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666921</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266922</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_003_0065</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846497" alias="UCSF_VRP_mNGS_027_0641">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846497</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_027_0641</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666922">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666922</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267498</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_027_0641</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846498" alias="UCSF_VRP_mNGS_027_0642">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846498</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_027_0642</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666923">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666923</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267499</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_027_0642</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846499" alias="UCSF_VRP_mNGS_027_0643">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846499</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_027_0643</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666926">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666926</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267500</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_027_0643</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846500" alias="UCSF_VRP_mNGS_027_0644">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846500</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_027_0644</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666925">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666925</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267501</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_027_0644</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846501" alias="UCSF_VRP_mNGS_028_0645">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846501</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_028_0645</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666928">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666928</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267502</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_028_0645</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846502" alias="UCSF_VRP_mNGS_028_0646">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846502</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_028_0646</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666927">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666927</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267503</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_028_0646</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846503" alias="UCSF_VRP_mNGS_028_0647">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846503</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_028_0647</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666930">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666930</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267504</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_028_0647</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846504" alias="UCSF_VRP_mNGS_028_0648">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846504</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_028_0648</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666929">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666929</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267505</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_028_0648</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846505" alias="UCSF_VRP_mNGS_028_0649">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846505</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_028_0649</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666932">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666932</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267506</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_028_0649</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846506" alias="UCSF_VRP_mNGS_028_0650">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846506</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_028_0650</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666931">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666931</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267507</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_028_0650</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846507" alias="UCSF_VRP_mNGS_003_0066">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846507</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_003_0066</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666933">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666933</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266923</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_003_0066</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846508" alias="UCSF_VRP_mNGS_028_0651">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846508</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_028_0651</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666934">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666934</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267508</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_028_0651</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846509" alias="UCSF_VRP_mNGS_028_0652">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846509</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_028_0652</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666936">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666936</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267509</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_028_0652</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846510" alias="UCSF_VRP_mNGS_029_0653">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846510</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_029_0653</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666937">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666937</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267510</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_029_0653</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846511" alias="UCSF_VRP_mNGS_029_0654">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846511</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_029_0654</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666935">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666935</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267511</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_029_0654</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846512" alias="UCSF_VRP_mNGS_029_0655">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846512</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_029_0655</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666938">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666938</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267512</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_029_0655</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846513" alias="UCSF_VRP_mNGS_029_0656">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846513</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_029_0656</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666939">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666939</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267513</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_029_0656</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846514" alias="UCSF_VRP_mNGS_029_0657">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846514</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_029_0657</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666940">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666940</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267514</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_029_0657</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846515" alias="UCSF_VRP_mNGS_029_0658">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846515</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_029_0658</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666941">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666941</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267515</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_029_0658</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846516" alias="UCSF_VRP_mNGS_029_0659">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846516</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_029_0659</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666942">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666942</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267516</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_029_0659</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846517" alias="UCSF_VRP_mNGS_029_0660">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846517</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_029_0660</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666944">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666944</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267517</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_029_0660</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846518" alias="UCSF_VRP_mNGS_003_0067">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846518</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_003_0067</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666946">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666946</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266924</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_003_0067</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846519" alias="UCSF_VRP_mNGS_030_0683">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846519</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_030_0683</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666943">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666943</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267540</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_030_0683</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846520" alias="UCSF_VRP_mNGS_030_0684">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846520</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_030_0684</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666945">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666945</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267541</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_030_0684</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846521" alias="UCSF_VRP_mNGS_030_0685">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846521</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_030_0685</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666950">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666950</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267542</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_030_0685</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846522" alias="UCSF_VRP_mNGS_030_0686">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846522</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_030_0686</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666948">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666948</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267543</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_030_0686</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846523" alias="UCSF_VRP_mNGS_030_0687">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846523</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_030_0687</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666947">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666947</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267544</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_030_0687</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846524" alias="UCSF_VRP_mNGS_030_0688">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846524</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_030_0688</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666951">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666951</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267545</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_030_0688</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846525" alias="UCSF_VRP_mNGS_030_0689">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846525</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_030_0689</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666952">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666952</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267546</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_030_0689</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846526" alias="UCSF_VRP_mNGS_030_0690">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846526</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_030_0690</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666949">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666949</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267547</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_030_0690</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846527" alias="UCSF_VRP_mNGS_003_0070">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846527</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_003_0070</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666954">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666954</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40266927</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_003_0070</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846528" alias="UCSF_VRP_mNGS_030_0691">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846528</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_030_0691</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666955">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666955</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267548</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_030_0691</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846529" alias="UCSF_VRP_mNGS_030_0692">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846529</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_030_0692</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666953">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666953</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267549</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_030_0692</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846530" alias="UCSF_VRP_mNGS_030_0693">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846530</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_030_0693</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666957">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666957</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267550</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_030_0693</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846531" alias="UCSF_VRP_mNGS_030_0694">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846531</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_030_0694</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666956">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666956</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267551</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_030_0694</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846532" alias="UCSF_VRP_mNGS_030_0695">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846532</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_030_0695</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666959">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666959</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267552</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_030_0695</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23846533" alias="UCSF_VRP_mNGS_030_0696">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23846533</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14290493">UCSF_VRP_mNGS_030_0696</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Respiratory_mNGS</TITLE>
    <STUDY_REF accession="SRP493531">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1084017</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Simultaneous reverse transcription of purified RNA and ribosomal RNA depletion were carried out followed by second strand cDNA synthesis. Complementary DNA was purified using AMPure XP beads and loaded on an automated library prep instrument (MagicPrep NGS, Tecan Genomics) to undergo end-repair, adapter ligation and barcoding, amplification (25 cycles) and purification.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20666958">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20666958</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40267553</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>UCSF_VRP_mNGS_030_0696</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
