<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX12639526" alias="aquavitas_E1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639526</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592892">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592892</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639527" alias="aquavitas_E2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639527</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592893">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592893</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639528" alias="aquavitas_E11">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639528</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592894">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592894</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E11</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639529" alias="aquavitas_E128">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639529</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E128</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592895">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592895</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E128</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E128</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639530" alias="aquavitas_E129">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639530</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E129</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592896">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592896</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E129</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E129</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639531" alias="aquavitas_E130">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639531</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E130</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592897">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592897</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E130</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E130</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639532" alias="aquavitas_E131">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639532</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E131</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592898">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592898</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E131</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E131</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639533" alias="aquavitas_E132">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639533</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E132</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592899">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592899</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E132</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E132</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639534" alias="aquavitas_E133">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639534</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E133</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592900">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592900</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E133</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E133</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639535" alias="aquavitas_E134">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639535</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E134</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592901">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592901</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E134</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E134</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639536" alias="aquavitas_E135">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639536</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E135</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592902">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592902</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E135</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E135</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639537" alias="aquavitas_E136">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639537</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E136</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592903">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592903</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E136</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E136</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639538" alias="aquavitas_E137">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639538</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E137</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592904">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592904</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E137</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E137</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639539" alias="aquavitas_E12">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639539</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592905">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592905</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E12</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639540" alias="aquavitas_E138">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639540</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E138</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592906">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592906</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E138</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E138</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639541" alias="aquavitas_E13">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639541</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592907">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592907</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E13</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639542" alias="aquavitas_E14">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639542</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592908">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592908</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E14</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639543" alias="aquavitas_E15">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639543</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592909">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592909</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E15</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639544" alias="aquavitas_E16">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639544</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592910">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592910</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E16</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639545" alias="aquavitas_E17">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639545</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592911">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592911</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E17</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639546" alias="aquavitas_E18">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639546</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592912">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592912</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E18</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639547" alias="aquavitas_E19">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639547</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592913">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592913</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E19</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639548" alias="aquavitas_E20">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639548</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592914">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592914</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E20</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639549" alias="aquavitas_E3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639549</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592915">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592915</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639550" alias="aquavitas_E21">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639550</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592916">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592916</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E21</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639551" alias="aquavitas_E22">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639551</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592917">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592917</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E22</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639552" alias="aquavitas_E23">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639552</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592918">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592918</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E23</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639553" alias="aquavitas_E24">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639553</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592919">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592919</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E24</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639554" alias="aquavitas_E25">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639554</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592920">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592920</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E25</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E25</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639555" alias="aquavitas_E26">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639555</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592921">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592921</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E26</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E26</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639556" alias="aquavitas_E27">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639556</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592922">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592922</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E27</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E27</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639557" alias="aquavitas_E28">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639557</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592923">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592923</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E28</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E28</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639558" alias="aquavitas_E29">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639558</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592924">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592924</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E29</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E29</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639559" alias="aquavitas_E30">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639559</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592925">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592925</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E30</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E30</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639560" alias="aquavitas_E4">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639560</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592926">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592926</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E4</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639561" alias="aquavitas_E31">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639561</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592927">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592927</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E31</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E31</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639562" alias="aquavitas_E33">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639562</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592928">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592928</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E33</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E33</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639563" alias="aquavitas_E34">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639563</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592929">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592929</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E34</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E34</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639564" alias="aquavitas_E35">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639564</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592930">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592930</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E35</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E35</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639565" alias="aquavitas_E36">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639565</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E36</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592931">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592931</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E36</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E36</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639566" alias="aquavitas_E37">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639566</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E37</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592932">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592932</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E37</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E37</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639567" alias="aquavitas_E38">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639567</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E38</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592933">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592933</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E38</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E38</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639568" alias="aquavitas_E39">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639568</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E39</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592934">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592934</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E39</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E39</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639569" alias="aquavitas_E40">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639569</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E40</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592935">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592935</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E40</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E40</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639570" alias="aquavitas_E41">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639570</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E41</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592936">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592936</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E41</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E41</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639571" alias="aquavitas_E5">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639571</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592937">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592937</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E5</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639572" alias="aquavitas_E42">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639572</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E42</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592938">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592938</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E42</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E42</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639573" alias="aquavitas_E43">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639573</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E43</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592939">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592939</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E43</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E43</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639574" alias="aquavitas_E44">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639574</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E44</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592940">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592940</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E44</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E44</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639575" alias="aquavitas_E51">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639575</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E51</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592941">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592941</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E51</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E51</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639576" alias="aquavitas_E52">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639576</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E52</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592942">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592942</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E52</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E52</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639577" alias="aquavitas_E53">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639577</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E53</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592943">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592943</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E53</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E53</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639578" alias="aquavitas_E54">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639578</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E54</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592944">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592944</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E54</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E54</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639579" alias="aquavitas_E55">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639579</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E55</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592945">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592945</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E55</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E55</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639580" alias="aquavitas_E56">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639580</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E56</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592946">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592946</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E56</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E56</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639581" alias="aquavitas_E57">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639581</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E57</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592947">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592947</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E57</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E57</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639582" alias="aquavitas_E6">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639582</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592948">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592948</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E6</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639583" alias="aquavitas_E58">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639583</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E58</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592949">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592949</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E58</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E58</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639584" alias="aquavitas_E59">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639584</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E59</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592950">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592950</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E59</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E59</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639585" alias="aquavitas_E60">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639585</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E60</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592951">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592951</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E60</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E60</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639586" alias="aquavitas_E61">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639586</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E61</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592952">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592952</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E61</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E61</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639587" alias="aquavitas_E62">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639587</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E62</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592953">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592953</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E62</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E62</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639588" alias="aquavitas_E63">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639588</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E63</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592954">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592954</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E63</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E63</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639589" alias="aquavitas_E64">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639589</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E64</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592955">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592955</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E64</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E64</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639590" alias="aquavitas_E65">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639590</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E65</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592956">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592956</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E65</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E65</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639591" alias="aquavitas_E66">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639591</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E66</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592957">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592957</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E66</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E66</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639592" alias="aquavitas_E67">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639592</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E67</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592958">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592958</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E67</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E67</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639593" alias="aquavitas_E7">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639593</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592959">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592959</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E7</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639594" alias="aquavitas_E68">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639594</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E68</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592960">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592960</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E68</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E68</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639595" alias="aquavitas_E75">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639595</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E75</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592961">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592961</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E75</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E75</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639596" alias="aquavitas_E76">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639596</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E76</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592962">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592962</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E76</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E76</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639597" alias="aquavitas_E77">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639597</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E77</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592963">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592963</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E77</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E77</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639598" alias="aquavitas_E78">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639598</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E78</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592964">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592964</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E78</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E78</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639599" alias="aquavitas_E79">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639599</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E79</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592965">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592965</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E79</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E79</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639600" alias="aquavitas_E80">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639600</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E80</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592966">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592966</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E80</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E80</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639601" alias="aquavitas_E81">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639601</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E81</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592967">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592967</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E81</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E81</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639602" alias="aquavitas_E82">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639602</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E82</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592968">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592968</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E82</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E82</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639603" alias="aquavitas_E84">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639603</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E84</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592969">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592969</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E84</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E84</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639604" alias="aquavitas_E8">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639604</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592970">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592970</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E8</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639605" alias="aquavitas_E85">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639605</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E85</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592971">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592971</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E85</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E85</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639606" alias="aquavitas_E86">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639606</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E86</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592972">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592972</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E86</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E86</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639607" alias="aquavitas_E87">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639607</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E87</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592973">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592973</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E87</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E87</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639608" alias="aquavitas_E101">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639608</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E101</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592974">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592974</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E101</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E101</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639609" alias="aquavitas_E102">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639609</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E102</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592975">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592975</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E102</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E102</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639610" alias="aquavitas_E103">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639610</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E103</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592976">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592976</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E103</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E103</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639611" alias="aquavitas_E104">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639611</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E104</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592977">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592977</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E104</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E104</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639612" alias="aquavitas_E105">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639612</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E105</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592978">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592978</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E105</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E105</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639613" alias="aquavitas_E106">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639613</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E106</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592980">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592980</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E106</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E106</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639614" alias="aquavitas_E107">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639614</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E107</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592979">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592979</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E107</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E107</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639615" alias="aquavitas_E9">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639615</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592981">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592981</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E9</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639616" alias="aquavitas_E108">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639616</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E108</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592982">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592982</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E108</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E108</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639617" alias="aquavitas_E109">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639617</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E109</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592983">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592983</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E109</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E109</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639618" alias="aquavitas_E110">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639618</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E110</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592984">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592984</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E110</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E110</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639619" alias="aquavitas_E111">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639619</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E111</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592985">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592985</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E111</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E111</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639620" alias="aquavitas_E112">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639620</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E112</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592986">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592986</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E112</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E112</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639621" alias="aquavitas_E113">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639621</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E113</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592987">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592987</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E113</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E113</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639622" alias="aquavitas_E114">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639622</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E114</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592988">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592988</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E114</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E114</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639623" alias="aquavitas_E115">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639623</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E115</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592989">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592989</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E115</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E115</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639624" alias="aquavitas_E116">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639624</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E116</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592990">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592990</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E116</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E116</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639625" alias="aquavitas_E117">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639625</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E117</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592991">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592991</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E117</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E117</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639626" alias="aquavitas_E10">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639626</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592992">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592992</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E10</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639627" alias="aquavitas_E118">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639627</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E118</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592993">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592993</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E118</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E118</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639628" alias="aquavitas_E119">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639628</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E119</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592994">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592994</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E119</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E119</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639629" alias="aquavitas_E120">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639629</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E120</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592995">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592995</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E120</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E120</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639630" alias="aquavitas_E121">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639630</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E121</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592996">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592996</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E121</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E121</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639631" alias="aquavitas_E122">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639631</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E122</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592997">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592997</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E122</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E122</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639632" alias="aquavitas_E123">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639632</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E123</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592998">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592998</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E123</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E123</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639633" alias="aquavitas_E124">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639633</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E124</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10592999">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10592999</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E124</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E124</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639634" alias="aquavitas_E125">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639634</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E125</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10593000">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10593000</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E125</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E125</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639635" alias="aquavitas_E126">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639635</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E126</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10593001">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10593001</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E126</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E126</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12639636" alias="aquavitas_E127">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12639636</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10524869">aquavitas_E127</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Genomic sequencing of SARS-CoV-2: Wastewater</TITLE>
    <STUDY_REF accession="SRP341648">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341648</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA771693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA extracted from wastewater samples is converted to cDNA using LunaScript RT SuperMix (NEB). Tiled amplicons will be generated by multiplex PCR using the Q5 Hot Start High-Fidelity 2X Master Mix (NEB) with the artic V4 primers (https://github.com/artic-network/artic-ncov2019/tree/master/primer_schemes/nCoV-2019/V4) then prepared for sequencing using the PlexWell 384 Library Prep Kit (SeqWell) following manufacturers instructions, or generated and prepared for sequencing using the Normalase SARS-CoV-2 Amplicon Panel (Swift Biosciences) following manufacturers instructions. Pooled libraries will be sequenced on a NextSeq500/550 (Illumina) at 2x150 targeting a total read count &gt;= 430k paired end reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10593002">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10593002</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|darwinw13">aquavitas_E127</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aquavitas_E127</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>VIRAL RNA</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
