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<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT alias="GSM2588868" accession="SRX2763788">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2763788</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2588868</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2588868: WT CD45+CD11chiSiglecF+CD11blo Macrophages 7 d.p.i. with N.brasiliensis; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP105184" refname="GSE98167">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105184</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
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      <SAMPLE_DESCRIPTOR accession="SRS2148352">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2148352</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2588868</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cell-sorted lung macrophages were lysed using QIAshredder Mini Spin Column (Qiagen, #79656) and RNA was extracted using RNeasy Mini Kit (Qiagen, #74106) following the manufacturer's instructions. mRNA was purified from approximately 500ng of total RNA with oligo-dT beads and sheared by incubation at 94C.  Following first-strand synthesis with random primers, second strand synthesis was performed with dUTP for generating strand-specific sequencing libraries.  The cDNA library was then end-repaired, and A-tailed, adapters were ligated and second-strand digestion was performed by Uracil-DNA-Glycosylase. Indexed libraries that met appropriate cut-offs for both were quantified by qRT-PCR using a commercially available kit (KAPA Biosystems) and insert size distribution determined with the LabChip GX or Agilent Bioanalyzer. Samples with a yield of ≥0.5 ng/ul were used for sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302588868</ID>
          <LABEL>GSM2588868</LABEL>
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  <EXPERIMENT alias="GSM2588869" accession="SRX2763789">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2763789</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2588869</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2588869: Axl-/-Mertk-/- CD45+CD11chiSiglecF+CD11blo Macrophages 7 d.p.i. with N. brasiliensis; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP105184" refname="GSE98167">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105184</PRIMARY_ID>
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      <SAMPLE_DESCRIPTOR accession="SRS2148353">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2148353</PRIMARY_ID>
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      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cell-sorted lung macrophages were lysed using QIAshredder Mini Spin Column (Qiagen, #79656) and RNA was extracted using RNeasy Mini Kit (Qiagen, #74106) following the manufacturer's instructions. mRNA was purified from approximately 500ng of total RNA with oligo-dT beads and sheared by incubation at 94C.  Following first-strand synthesis with random primers, second strand synthesis was performed with dUTP for generating strand-specific sequencing libraries.  The cDNA library was then end-repaired, and A-tailed, adapters were ligated and second-strand digestion was performed by Uracil-DNA-Glycosylase. Indexed libraries that met appropriate cut-offs for both were quantified by qRT-PCR using a commercially available kit (KAPA Biosystems) and insert size distribution determined with the LabChip GX or Agilent Bioanalyzer. Samples with a yield of ≥0.5 ng/ul were used for sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
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    <EXPERIMENT_LINKS>
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        <XREF_LINK>
          <DB>gds</DB>
          <ID>302588869</ID>
          <LABEL>GSM2588869</LABEL>
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    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2588869</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
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