<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX18259541" alias="Roseibium sp. Sym1- 16S rDNA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18259541</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12179284">Roseibium sp. Sym1- 16S rDNA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Roseibium sp. strain Sym1, 16S ribosomal RNA gene, partial sequence</TITLE>
    <STUDY_REF accession="SRP399743">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP399743</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA884430</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Bacteria were isolated from a 3-year Symbiodiniaceae linucheae culture and cultured using dilution-to-extinction method on marine R2A, followed by DNA extraction using the GenElute Bacterial Genomic DNA kit and the 16s rRNA gene Sanger sequenced by using the 27F/1492R primers. Two contigs joined together using GeneStudio's contig editor on default settings.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS15246653">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15246653</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN31026946</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Roseibium sp. Sym1- 16S rDNA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <CAPILLARY>
        <INSTRUMENT_MODEL>AB 3730xL Genetic Analyzer</INSTRUMENT_MODEL>
      </CAPILLARY>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
