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          <dc:title>&lt;p&gt;Findings in mNGS sequencing.&lt;/p&gt;</dc:title>
          <dc:creator>Erika Stentoft (10113615)</dc:creator>
          <dc:creator>Josefin Olausson (3966890)</dc:creator>
          <dc:creator>Emilio Rudbeck (19859283)</dc:creator>
          <dc:creator>Marie Studahl (2806312)</dc:creator>
          <dc:creator>Hedvig E. Jakobsson (7818818)</dc:creator>
          <dc:subject>Medicine</dc:subject>
          <dc:subject>Microbiology</dc:subject>
          <dc:subject>Cell Biology</dc:subject>
          <dc:subject>Neuroscience</dc:subject>
          <dc:subject>Environmental Sciences not elsewhere classified</dc:subject>
          <dc:subject>Ecology</dc:subject>
          <dc:subject>Immunology</dc:subject>
          <dc:subject>Biological Sciences not elsewhere classified</dc:subject>
          <dc:subject>Cancer</dc:subject>
          <dc:subject>Infectious Diseases</dc:subject>
          <dc:subject>Virology</dc:subject>
          <dc:subject>swedish national guidelines</dc:subject>
          <dc:subject>one csf sample</dc:subject>
          <dc:subject>ion torrent platform</dc:subject>
          <dc:subject>common autoimmune antibodies</dc:subject>
          <dc:subject>cerebrospinal fluid samples</dc:subject>
          <dc:subject>mngs might detect</dc:subject>
          <dc:subject>17 csf samples</dc:subject>
          <dc:subject>xlink "&gt;</dc:subject>
          <dc:subject>viral agents</dc:subject>
          <dc:subject>unknown origin</dc:subject>
          <dc:subject>unknown etiology</dc:subject>
          <dc:subject>safe implementation</dc:subject>
          <dc:subject>primary aim</dc:subject>
          <dc:subject>metagenomic sequencing</dc:subject>
          <dc:subject>main conclusion</dc:subject>
          <dc:subject>known virus</dc:subject>
          <dc:subject>human pegivirus</dc:subject>
          <dc:subject>generation sequencing</dc:subject>
          <dc:subject>cns infections</dc:subject>
          <dc:subject>close collaboration</dc:subject>
          <dc:subject>clinicians enables</dc:subject>
          <dc:subject>clinical laboratory</dc:subject>
          <dc:subject>11 ).</dc:subject>
          <dc:description>&lt;p&gt;Sequencing reads from all samples sequenced in order of runs. Table is divided to show results from DNA, as well as long and short fragmentation time of RNA. Patient samples, Control patient samples and cell line controls are included in each of the eight sequencing runs.&lt;/p&gt; &lt;p&gt;(XLSX)&lt;/p&gt;</dc:description>
          <dc:date>2026-09-15T17:50:50Z</dc:date>
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          <dc:identifier>10.1371/journal.pone.0358189.s002</dc:identifier>
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