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    </IDENTIFIERS>
    <TITLE>GSM5631661: CTCL lesion of patient 34 [34A]; organismal metagenomes; miRNA-Seq</TITLE>
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      <IDENTIFIERS>
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        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
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        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
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        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
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        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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  <EXPERIMENT alias="GSM5631662" accession="SRX12678049">
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      <PRIMARY_ID>SRX12678049</PRIMARY_ID>
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    <TITLE>GSM5631662: CTCL lesion of patient 36 [36A]; organismal metagenomes; miRNA-Seq</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
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          <PRIMARY_ID>SRS10629543</PRIMARY_ID>
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        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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          <ID>305631662</ID>
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  <EXPERIMENT alias="GSM5631663" accession="SRX12678050">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678050</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631663</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631663: CTCL lesion of patient 37 [37A]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
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      <DESIGN_DESCRIPTION/>
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          <PRIMARY_ID>SRS10629544</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631663</EXTERNAL_ID>
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      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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  <EXPERIMENT alias="GSM5631664" accession="SRX12678051">
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      <PRIMARY_ID>SRX12678051</PRIMARY_ID>
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    <TITLE>GSM5631664: CTCL lesion of patient 38 [38A]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
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      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629545">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629545</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631664</EXTERNAL_ID>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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  <EXPERIMENT alias="GSM5631665" accession="SRX12678052">
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      <PRIMARY_ID>SRX12678052</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631665</SUBMITTER_ID>
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    <TITLE>GSM5631665: CTCL lesion of patient 39 [39A]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
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      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629546">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629546</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631665</EXTERNAL_ID>
        </IDENTIFIERS>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
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  <EXPERIMENT alias="GSM5631666" accession="SRX12678053">
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      <PRIMARY_ID>SRX12678053</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631666</SUBMITTER_ID>
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    <TITLE>GSM5631666: CTCL lesion of patient 40 [40A]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
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    <EXPERIMENT_LINKS>
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          <DB>gds</DB>
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  <EXPERIMENT alias="GSM5631667" accession="SRX12678054">
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      <PRIMARY_ID>SRX12678054</PRIMARY_ID>
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    <TITLE>GSM5631667: matched normal skin of patient 1 [1B]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
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          <DB>gds</DB>
          <ID>305631667</ID>
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  <EXPERIMENT alias="GSM5631668" accession="SRX12678055">
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      <PRIMARY_ID>SRX12678055</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631668</SUBMITTER_ID>
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    <TITLE>GSM5631668: matched normal skin of patient 2 [2B]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631668</ID>
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      <PRIMARY_ID>SRX12678056</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631669</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631669: matched normal skin of patient 3 [3B]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629550</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631669</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631669</ID>
          <LABEL>GSM5631669</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631669</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631670" accession="SRX12678057">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678057</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631670</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631670: matched normal skin of patient 4 [4B]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629551">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629551</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631670</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631670</ID>
          <LABEL>GSM5631670</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631670</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631671" accession="SRX12678058">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678058</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631671</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631671: matched normal skin of patient 5 [5B]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629552">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629552</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631671</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631671</ID>
          <LABEL>GSM5631671</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631671</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631672" accession="SRX12678059">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678059</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631672</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631672: matched normal skin of patient 6 [6B]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629553">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629553</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631672</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631672</ID>
          <LABEL>GSM5631672</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631672</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631673" accession="SRX12678060">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678060</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631673</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631673: matched normal skin of patient 7 [7B]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629554">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629554</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631673</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631673</ID>
          <LABEL>GSM5631673</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631673</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631674" accession="SRX12678061">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678061</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631674</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631674: matched normal skin of patient 8 [8B]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629555">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629555</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631674</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631674</ID>
          <LABEL>GSM5631674</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631674</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631675" accession="SRX12678062">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678062</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631675</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631675: matched normal skin of patient 9 [9B]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629556">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629556</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631675</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631675</ID>
          <LABEL>GSM5631675</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631675</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631676" accession="SRX12678063">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678063</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631676</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631676: matched normal skin of patient 10 [10B]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629557">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629557</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631676</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631676</ID>
          <LABEL>GSM5631676</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631676</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631628" accession="SRX12678064">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678064</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631628</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631628: CTCL lesion of patient 1  [1A]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629559">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629559</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631628</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631628</ID>
          <LABEL>GSM5631628</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631628</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631677" accession="SRX12678065">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678065</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631677</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631677: matched normal skin of patient 11 [11B]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629558">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629558</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631677</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631677</ID>
          <LABEL>GSM5631677</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631677</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631678" accession="SRX12678066">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678066</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631678</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631678: matched normal skin of patient 12 [12B]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629561">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629561</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631678</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631678</ID>
          <LABEL>GSM5631678</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631678</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631679" accession="SRX12678067">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678067</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631679</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631679: matched normal skin of patient 13 [13B]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629560">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629560</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631679</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631679</ID>
          <LABEL>GSM5631679</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631679</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631680" accession="SRX12678068">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678068</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631680</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631680: matched normal skin of patient 14 [14B]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629562">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629562</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631680</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631680</ID>
          <LABEL>GSM5631680</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631680</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631681" accession="SRX12678069">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678069</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631681</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631681: matched normal skin of patient 15 [15B]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629563">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629563</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631681</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631681</ID>
          <LABEL>GSM5631681</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631681</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631682" accession="SRX12678070">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678070</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631682</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631682: matched normal skin of patient 16 [16B]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629564">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629564</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631682</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631682</ID>
          <LABEL>GSM5631682</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631682</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631683" accession="SRX12678071">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678071</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631683</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631683: matched normal skin of patient 17 [17B]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629565">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629565</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631683</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631683</ID>
          <LABEL>GSM5631683</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631683</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631684" accession="SRX12678072">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678072</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631684</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631684: matched normal skin of patient 18 [18B]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629567">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629567</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631684</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631684</ID>
          <LABEL>GSM5631684</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631684</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631685" accession="SRX12678073">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678073</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631685</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631685: matched normal skin of patient 19 [19B]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629566">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629566</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631685</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631685</ID>
          <LABEL>GSM5631685</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631685</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631686" accession="SRX12678074">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678074</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631686</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631686: matched normal skin of patient 20 [20B]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629568">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629568</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631686</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631686</ID>
          <LABEL>GSM5631686</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631686</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631687" accession="SRX12678075">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678075</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631687</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631687: matched normal skin of patient 21 [21B]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629569">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629569</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631687</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631687</ID>
          <LABEL>GSM5631687</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631687</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631688" accession="SRX12678076">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678076</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631688</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631688: matched normal skin of patient 22 [22B]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629570">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629570</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631688</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631688</ID>
          <LABEL>GSM5631688</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631688</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631689" accession="SRX12678077">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678077</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631689</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631689: matched normal skin of patient 23 [23B]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629572">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629572</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631689</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631689</ID>
          <LABEL>GSM5631689</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631689</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631690" accession="SRX12678078">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678078</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631690</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631690: matched normal skin of patient 24 [24B]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629571">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629571</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631690</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631690</ID>
          <LABEL>GSM5631690</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631690</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631691" accession="SRX12678079">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678079</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631691</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631691: matched normal skin of patient 25 [25B]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629573">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629573</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631691</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631691</ID>
          <LABEL>GSM5631691</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631691</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631692" accession="SRX12678080">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678080</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631692</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631692: matched normal skin of patient 26 [26B]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629575">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629575</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631692</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631692</ID>
          <LABEL>GSM5631692</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631692</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631693" accession="SRX12678081">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678081</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631693</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631693: matched normal skin of patient 27 [27B]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629574">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629574</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631693</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631693</ID>
          <LABEL>GSM5631693</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631693</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631694" accession="SRX12678082">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678082</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631694</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631694: matched normal skin of patient 28 [28B]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629576">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629576</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631694</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631694</ID>
          <LABEL>GSM5631694</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631694</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631695" accession="SRX12678083">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678083</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631695</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631695: matched normal skin of patient 29 [29B]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629577">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629577</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631695</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631695</ID>
          <LABEL>GSM5631695</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631695</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631696" accession="SRX12678084">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678084</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631696</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631696: matched normal skin of patient 30 [30B]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629578">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629578</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631696</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631696</ID>
          <LABEL>GSM5631696</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631696</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631697" accession="SRX12678085">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678085</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631697</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631697: matched normal skin of patient 31 [31B]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629579">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629579</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631697</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631697</ID>
          <LABEL>GSM5631697</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631697</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631698" accession="SRX12678086">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678086</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631698</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631698: matched normal skin of patient 32 [32B]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629580">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629580</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631698</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631698</ID>
          <LABEL>GSM5631698</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631698</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631699" accession="SRX12678087">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678087</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631699</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631699: matched normal skin of patient 33 [33B]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629581">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629581</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631699</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631699</ID>
          <LABEL>GSM5631699</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631699</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631700" accession="SRX12678088">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678088</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631700</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631700: matched normal skin of patient 34 [34B]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629582">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629582</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631700</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631700</ID>
          <LABEL>GSM5631700</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631700</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631701" accession="SRX12678089">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678089</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631701</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631701: matched normal skin of patient 36 [36B]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629583">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629583</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631701</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631701</ID>
          <LABEL>GSM5631701</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631701</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631702" accession="SRX12678090">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678090</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631702</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631702: matched normal skin of patient 37 [37B]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629585">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629585</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631702</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631702</ID>
          <LABEL>GSM5631702</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631702</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631703" accession="SRX12678091">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678091</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631703</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631703: matched normal skin of patient 38 [38B]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629584">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629584</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631703</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631703</ID>
          <LABEL>GSM5631703</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631703</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631704" accession="SRX12678092">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678092</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631704</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631704: matched normal skin of patient 39 [39B]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629586">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629586</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631704</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631704</ID>
          <LABEL>GSM5631704</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631704</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631705" accession="SRX12678093">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678093</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631705</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631705: matched normal skin of patient 40 [40B]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629587">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629587</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631705</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631705</ID>
          <LABEL>GSM5631705</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631705</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631629" accession="SRX12678094">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678094</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631629</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631629: CTCL lesion of patient 2 [2A]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629588">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629588</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631629</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631629</ID>
          <LABEL>GSM5631629</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631629</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631630" accession="SRX12678095">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678095</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631630</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631630: CTCL lesion of patient 3 [3A]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629589">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629589</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631630</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631630</ID>
          <LABEL>GSM5631630</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631630</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631631" accession="SRX12678096">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678096</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631631</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631631: CTCL lesion of patient 4 [4A]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629590">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629590</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631631</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631631</ID>
          <LABEL>GSM5631631</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631631</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631632" accession="SRX12678097">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678097</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631632</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631632: CTCL lesion of patient 5 [5A]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629591">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629591</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631632</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631632</ID>
          <LABEL>GSM5631632</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631632</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631633" accession="SRX12678098">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678098</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631633</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631633: CTCL lesion of patient 6 [6A]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629592">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629592</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631633</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631633</ID>
          <LABEL>GSM5631633</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631633</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631634" accession="SRX12678099">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678099</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631634</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631634: CTCL lesion of patient 7 [7A]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629593">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629593</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631634</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631634</ID>
          <LABEL>GSM5631634</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631634</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631635" accession="SRX12678100">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678100</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631635</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631635: CTCL lesion of patient 8 [8A]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629594">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629594</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631635</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631635</ID>
          <LABEL>GSM5631635</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631635</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631636" accession="SRX12678101">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678101</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631636</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631636: CTCL lesion of patient 9 [9A]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629595">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629595</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631636</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631636</ID>
          <LABEL>GSM5631636</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631636</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631637" accession="SRX12678102">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678102</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631637</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631637: CTCL lesion of patient 10 [10A]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629596">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629596</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631637</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631637</ID>
          <LABEL>GSM5631637</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631637</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631638" accession="SRX12678103">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678103</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631638</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631638: CTCL lesion of patient 11 [11A]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629597">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629597</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631638</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631638</ID>
          <LABEL>GSM5631638</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631638</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631639" accession="SRX12678104">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678104</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631639</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631639: CTCL lesion of patient 12 [12A]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629598">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629598</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631639</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631639</ID>
          <LABEL>GSM5631639</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631639</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631640" accession="SRX12678105">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678105</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631640</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631640: CTCL lesion of patient 13 [13A]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629599">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629599</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631640</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631640</ID>
          <LABEL>GSM5631640</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631640</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631641" accession="SRX12678106">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678106</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631641</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631641: CTCL lesion of patient 14 [14A]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629600">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629600</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631641</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631641</ID>
          <LABEL>GSM5631641</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631641</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631642" accession="SRX12678107">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678107</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631642</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631642: CTCL lesion of patient 15 [15A]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629601">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629601</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631642</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631642</ID>
          <LABEL>GSM5631642</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631642</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631643" accession="SRX12678108">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678108</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631643</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631643: CTCL lesion of patient 16 [16A]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629602">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629602</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631643</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631643</ID>
          <LABEL>GSM5631643</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631643</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631644" accession="SRX12678109">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678109</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631644</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631644: CTCL lesion of patient 17 [17A]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629603">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629603</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631644</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631644</ID>
          <LABEL>GSM5631644</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631644</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631645" accession="SRX12678110">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678110</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631645</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631645: CTCL lesion of patient 18 [18A]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629604">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629604</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631645</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631645</ID>
          <LABEL>GSM5631645</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631645</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631646" accession="SRX12678111">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678111</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631646</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631646: CTCL lesion of patient 19 [19A]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629605">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629605</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631646</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631646</ID>
          <LABEL>GSM5631646</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631646</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631647" accession="SRX12678112">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678112</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631647</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631647: CTCL lesion of patient 20 [20A]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629606">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629606</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631647</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631647</ID>
          <LABEL>GSM5631647</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631647</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631648" accession="SRX12678113">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678113</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631648</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631648: CTCL lesion of patient 21 [21A]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629607">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629607</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631648</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631648</ID>
          <LABEL>GSM5631648</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631648</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631649" accession="SRX12678114">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678114</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631649</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631649: CTCL lesion of patient 22 [22A]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629608">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629608</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631649</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631649</ID>
          <LABEL>GSM5631649</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631649</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631650" accession="SRX12678115">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678115</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631650</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631650: CTCL lesion of patient 23 [23A]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629609">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629609</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631650</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631650</ID>
          <LABEL>GSM5631650</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631650</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631651" accession="SRX12678116">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678116</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631651</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631651: CTCL lesion of patient 24 [24A]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629610">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629610</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631651</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631651</ID>
          <LABEL>GSM5631651</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631651</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631652" accession="SRX12678117">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678117</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631652</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631652: CTCL lesion of patient 25 [25A]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629611">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629611</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631652</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631652</ID>
          <LABEL>GSM5631652</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631652</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631653" accession="SRX12678118">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678118</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631653</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631653: CTCL lesion of patient 26 [26A]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629612">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629612</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631653</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631653</ID>
          <LABEL>GSM5631653</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631653</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631654" accession="SRX12678119">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678119</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631654</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631654: CTCL lesion of patient 27 [27A]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629613">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629613</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631654</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631654</ID>
          <LABEL>GSM5631654</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631654</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631655" accession="SRX12678120">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678120</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631655</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631655: CTCL lesion of patient 28 [28A]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629614">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629614</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631655</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631655</ID>
          <LABEL>GSM5631655</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631655</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631656" accession="SRX12678121">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678121</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631656</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631656: CTCL lesion of patient 29 [29A]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629615">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629615</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631656</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631656</ID>
          <LABEL>GSM5631656</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631656</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631657" accession="SRX12678122">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678122</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631657</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631657: CTCL lesion of patient 30 [30A]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629616">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629616</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631657</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631657</ID>
          <LABEL>GSM5631657</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631657</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631658" accession="SRX12678123">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678123</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631658</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631658: CTCL lesion of patient 31 [31A]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629617">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629617</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631658</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631658</ID>
          <LABEL>GSM5631658</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631658</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631659" accession="SRX12678124">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678124</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631659</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631659: CTCL lesion of patient 32 [32A]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629618">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629618</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631659</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631659</ID>
          <LABEL>GSM5631659</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631659</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5631660" accession="SRX12678125">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12678125</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5631660</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631660: CTCL lesion of patient 33 [33A]; organismal metagenomes; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP341991" refname="GSE186083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341991</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10629619">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10629619</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631660</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>MicrobiomeInsight did the extraction. DNA is extracted from samples using the Qiagen MagAttract PowerSoil DNA KF Kit (Formerly MO BIO PowerSoil DNA Kit) optimized for the Thermofisher KingFisher robot. This kit uses magnetic beads to specifically capture DNA while excluding organic inhibitors. In-house testing has shown this kit to have a good balance of DNA yield and quality as demonstrated on a variety of environmental sample types. DNA quantification and quality checks are done via Qubit. The high-fidelity Phusion polymerase for amplification of marker genes will be used. If extractions contain some carry-over inhibition or a high concentration of DNA, typically1:1 and 1:10 dilutions will be tested and run the PCR products on gels for verification. PCR is done with dual-barcoded primers targeting either the prokaryotic 16S DNA with modified V4 skin cutaneous microbiome protocol. Samples with failed PCRs (or spurious bands) are re-amplified by optimizing PCR conditions. The PCR reactions are cleaned-up and normalized using the high-throughput SequalPrep 96-well Plate Kit. Samples are then pooled to make one library that is quantified accurately with the KAPA qPCR Library Quant kit. Library pools are sequenced on the Illumina MiSeq using the corresponding primer sets for prokaryotic 16S V4_skin.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305631660</ID>
          <LABEL>GSM5631660</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5631660</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
</EXPERIMENT_SET>
