<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX2774783" alias="BRC10-50">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2774783</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2620010">BRC10-50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA sequencing of Escherichia coli: bottleneck relief control line 10, day 50</TITLE>
    <STUDY_REF accession="SRP105908">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105908</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA385021</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Samples were streaked to single colonies on LB agar. Single colonies were then used to inoculate LB liquid media. Genomic DNA was isolated using the Wizard Genomic DNA Purification Kit (Promega), and quantified using the Nanodrop 1000 Spectrophotometer and Qubit 2.0 Fluorometer. Sequencing was carried out by Macrogen Korea using an Illumina MiSeq platform with 2x250bp paired end reads. All 15 evolved samples were multiplexed in a single Illumina MiSeq Lane.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2158093">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2158093</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|nwheeler443">BRC10-50</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>BRC10-50</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2774784" alias="BRC9-50">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2774784</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2620010">BRC9-50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA sequencing of Escherichia coli: bottleneck relief control line 9, day 50</TITLE>
    <STUDY_REF accession="SRP105908">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105908</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA385021</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Samples were streaked to single colonies on LB agar. Single colonies were then used to inoculate LB liquid media. Genomic DNA was isolated using the Wizard Genomic DNA Purification Kit (Promega), and quantified using the Nanodrop 1000 Spectrophotometer and Qubit 2.0 Fluorometer. Sequencing was carried out by Macrogen Korea using an Illumina MiSeq platform with 2x250bp paired end reads. All 15 evolved samples were multiplexed in a single Illumina MiSeq Lane.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2158094">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2158094</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|nwheeler443">BRC9-50</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>BRC9-50</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2774785" alias="BRC8-50">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2774785</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2620010">BRC8-50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA sequencing of Escherichia coli: bottleneck relief control line 8, day 50</TITLE>
    <STUDY_REF accession="SRP105908">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105908</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA385021</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Samples were streaked to single colonies on LB agar. Single colonies were then used to inoculate LB liquid media. Genomic DNA was isolated using the Wizard Genomic DNA Purification Kit (Promega), and quantified using the Nanodrop 1000 Spectrophotometer and Qubit 2.0 Fluorometer. Sequencing was carried out by Macrogen Korea using an Illumina MiSeq platform with 2x250bp paired end reads. All 15 evolved samples were multiplexed in a single Illumina MiSeq Lane.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2158095">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2158095</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|nwheeler443">BRC8-50</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>BRC8-50</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2774786" alias="BRC7-50">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2774786</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2620010">BRC7-50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA sequencing of Escherichia coli: bottleneck relief control line 7, day 50</TITLE>
    <STUDY_REF accession="SRP105908">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105908</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA385021</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Samples were streaked to single colonies on LB agar. Single colonies were then used to inoculate LB liquid media. Genomic DNA was isolated using the Wizard Genomic DNA Purification Kit (Promega), and quantified using the Nanodrop 1000 Spectrophotometer and Qubit 2.0 Fluorometer. Sequencing was carried out by Macrogen Korea using an Illumina MiSeq platform with 2x250bp paired end reads. All 15 evolved samples were multiplexed in a single Illumina MiSeq Lane.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2158096">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2158096</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|nwheeler443">BRC7-50</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>BRC7-50</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2774787" alias="BRC6-50">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2774787</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2620010">BRC6-50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA sequencing of Escherichia coli: bottleneck relief control line 6, day 50</TITLE>
    <STUDY_REF accession="SRP105908">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105908</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA385021</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Samples were streaked to single colonies on LB agar. Single colonies were then used to inoculate LB liquid media. Genomic DNA was isolated using the Wizard Genomic DNA Purification Kit (Promega), and quantified using the Nanodrop 1000 Spectrophotometer and Qubit 2.0 Fluorometer. Sequencing was carried out by Macrogen Korea using an Illumina MiSeq platform with 2x250bp paired end reads. All 15 evolved samples were multiplexed in a single Illumina MiSeq Lane.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2158097">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2158097</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|nwheeler443">BRC6-50</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>BRC6-50</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2774788" alias="BRC5-50">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2774788</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2620010">BRC5-50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA sequencing of Escherichia coli: bottleneck relief control line 5, day 50</TITLE>
    <STUDY_REF accession="SRP105908">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105908</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA385021</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Samples were streaked to single colonies on LB agar. Single colonies were then used to inoculate LB liquid media. Genomic DNA was isolated using the Wizard Genomic DNA Purification Kit (Promega), and quantified using the Nanodrop 1000 Spectrophotometer and Qubit 2.0 Fluorometer. Sequencing was carried out by Macrogen Korea using an Illumina MiSeq platform with 2x250bp paired end reads. All 15 evolved samples were multiplexed in a single Illumina MiSeq Lane.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2158098">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2158098</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|nwheeler443">BRC5-50</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>BRC5-50</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2774789" alias="BRC4-50">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2774789</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2620010">BRC4-50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA sequencing of Escherichia coli: bottleneck relief control line 4, day 50</TITLE>
    <STUDY_REF accession="SRP105908">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105908</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA385021</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Samples were streaked to single colonies on LB agar. Single colonies were then used to inoculate LB liquid media. Genomic DNA was isolated using the Wizard Genomic DNA Purification Kit (Promega), and quantified using the Nanodrop 1000 Spectrophotometer and Qubit 2.0 Fluorometer. Sequencing was carried out by Macrogen Korea using an Illumina MiSeq platform with 2x250bp paired end reads. All 15 evolved samples were multiplexed in a single Illumina MiSeq Lane.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2158099">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2158099</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|nwheeler443">BRC4-50</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>BRC4-50</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2774790" alias="BRC3-50">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2774790</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2620010">BRC3-50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA sequencing of Escherichia coli: bottleneck relief control line 3, day 50</TITLE>
    <STUDY_REF accession="SRP105908">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105908</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA385021</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Samples were streaked to single colonies on LB agar. Single colonies were then used to inoculate LB liquid media. Genomic DNA was isolated using the Wizard Genomic DNA Purification Kit (Promega), and quantified using the Nanodrop 1000 Spectrophotometer and Qubit 2.0 Fluorometer. Sequencing was carried out by Macrogen Korea using an Illumina MiSeq platform with 2x250bp paired end reads. All 15 evolved samples were multiplexed in a single Illumina MiSeq Lane.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2158100">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2158100</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|nwheeler443">BRC3-50</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>BRC3-50</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2774791" alias="BRC1-50">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2774791</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2620010">BRC1-50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA sequencing of Escherichia coli: bottleneck relief control line 1, day 50</TITLE>
    <STUDY_REF accession="SRP105908">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105908</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA385021</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Samples were streaked to single colonies on LB agar. Single colonies were then used to inoculate LB liquid media. Genomic DNA was isolated using the Wizard Genomic DNA Purification Kit (Promega), and quantified using the Nanodrop 1000 Spectrophotometer and Qubit 2.0 Fluorometer. Sequencing was carried out by Macrogen Korea using an Illumina MiSeq platform with 2x250bp paired end reads. All 15 evolved samples were multiplexed in a single Illumina MiSeq Lane.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2158101">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2158101</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|nwheeler443">BRC1-50</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>BRC1-50</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2774792" alias="BR10-50">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2774792</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2620010">BR10-50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA sequencing of Escherichia coli: bottleneck relief line 10, day 50</TITLE>
    <STUDY_REF accession="SRP105908">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105908</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA385021</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Samples were streaked to single colonies on LB agar. Single colonies were then used to inoculate LB liquid media. Genomic DNA was isolated using the Wizard Genomic DNA Purification Kit (Promega), and quantified using the Nanodrop 1000 Spectrophotometer and Qubit 2.0 Fluorometer. Sequencing was carried out by Macrogen Korea using an Illumina MiSeq platform with 2x250bp paired end reads. All 15 evolved samples were multiplexed in a single Illumina MiSeq Lane.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2158102">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2158102</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|nwheeler443">BR10-50</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>BR10-50</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2774793" alias="BR9-50">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2774793</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2620010">BR9-50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA sequencing of Escherichia coli: bottleneck relief line 9, day 50</TITLE>
    <STUDY_REF accession="SRP105908">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105908</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA385021</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Samples were streaked to single colonies on LB agar. Single colonies were then used to inoculate LB liquid media. Genomic DNA was isolated using the Wizard Genomic DNA Purification Kit (Promega), and quantified using the Nanodrop 1000 Spectrophotometer and Qubit 2.0 Fluorometer. Sequencing was carried out by Macrogen Korea using an Illumina MiSeq platform with 2x250bp paired end reads. All 15 evolved samples were multiplexed in a single Illumina MiSeq Lane.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2158103">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2158103</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|nwheeler443">BR9-50</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>BR9-50</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2774794" alias="BR8-50">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2774794</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2620010">BR8-50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA sequencing of Escherichia coli: bottleneck relief line 8, day 50</TITLE>
    <STUDY_REF accession="SRP105908">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105908</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA385021</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Samples were streaked to single colonies on LB agar. Single colonies were then used to inoculate LB liquid media. Genomic DNA was isolated using the Wizard Genomic DNA Purification Kit (Promega), and quantified using the Nanodrop 1000 Spectrophotometer and Qubit 2.0 Fluorometer. Sequencing was carried out by Macrogen Korea using an Illumina MiSeq platform with 2x250bp paired end reads. All 15 evolved samples were multiplexed in a single Illumina MiSeq Lane.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2158104">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2158104</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|nwheeler443">BR8-50</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>BR8-50</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2774795" alias="BR7-50">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2774795</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2620010">BR7-50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA sequencing of Escherichia coli: bottleneck relief line 7, day 50</TITLE>
    <STUDY_REF accession="SRP105908">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105908</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA385021</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Samples were streaked to single colonies on LB agar. Single colonies were then used to inoculate LB liquid media. Genomic DNA was isolated using the Wizard Genomic DNA Purification Kit (Promega), and quantified using the Nanodrop 1000 Spectrophotometer and Qubit 2.0 Fluorometer. Sequencing was carried out by Macrogen Korea using an Illumina MiSeq platform with 2x250bp paired end reads. All 15 evolved samples were multiplexed in a single Illumina MiSeq Lane.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2158105">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2158105</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|nwheeler443">BR7-50</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>BR7-50</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2774796" alias="BR6-50">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2774796</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2620010">BR6-50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA sequencing of Escherichia coli: bottleneck relief line 6, day 50</TITLE>
    <STUDY_REF accession="SRP105908">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105908</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA385021</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Samples were streaked to single colonies on LB agar. Single colonies were then used to inoculate LB liquid media. Genomic DNA was isolated using the Wizard Genomic DNA Purification Kit (Promega), and quantified using the Nanodrop 1000 Spectrophotometer and Qubit 2.0 Fluorometer. Sequencing was carried out by Macrogen Korea using an Illumina MiSeq platform with 2x250bp paired end reads. All 15 evolved samples were multiplexed in a single Illumina MiSeq Lane.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2158106">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2158106</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|nwheeler443">BR6-50</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>BR6-50</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2774797" alias="BR4-50">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2774797</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2620010">BR4-50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA sequencing of Escherichia coli: bottleneck relief line 4, day 50</TITLE>
    <STUDY_REF accession="SRP105908">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105908</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA385021</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Samples were streaked to single colonies on LB agar. Single colonies were then used to inoculate LB liquid media. Genomic DNA was isolated using the Wizard Genomic DNA Purification Kit (Promega), and quantified using the Nanodrop 1000 Spectrophotometer and Qubit 2.0 Fluorometer. Sequencing was carried out by Macrogen Korea using an Illumina MiSeq platform with 2x250bp paired end reads. All 15 evolved samples were multiplexed in a single Illumina MiSeq Lane.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2158107">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2158107</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|nwheeler443">BR4-50</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>BR4-50</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2774798" alias="BR3-50">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2774798</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2620010">BR3-50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA sequencing of Escherichia coli: bottleneck relief line 3, day 50</TITLE>
    <STUDY_REF accession="SRP105908">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105908</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA385021</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Samples were streaked to single colonies on LB agar. Single colonies were then used to inoculate LB liquid media. Genomic DNA was isolated using the Wizard Genomic DNA Purification Kit (Promega), and quantified using the Nanodrop 1000 Spectrophotometer and Qubit 2.0 Fluorometer. Sequencing was carried out by Macrogen Korea using an Illumina MiSeq platform with 2x250bp paired end reads. All 15 evolved samples were multiplexed in a single Illumina MiSeq Lane.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2158108">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2158108</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|nwheeler443">BR3-50</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>BR3-50</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2774799" alias="BR2-50">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2774799</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2620010">BR2-50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA sequencing of Escherichia coli: bottleneck relief line 2, day 50</TITLE>
    <STUDY_REF accession="SRP105908">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105908</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA385021</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Samples were streaked to single colonies on LB agar. Single colonies were then used to inoculate LB liquid media. Genomic DNA was isolated using the Wizard Genomic DNA Purification Kit (Promega), and quantified using the Nanodrop 1000 Spectrophotometer and Qubit 2.0 Fluorometer. Sequencing was carried out by Macrogen Korea using an Illumina MiSeq platform with 2x250bp paired end reads. All 15 evolved samples were multiplexed in a single Illumina MiSeq Lane.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2158110">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2158110</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|nwheeler443">BR2-50</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>BR2-50</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2774800" alias="BR1-50">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2774800</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2620010">BR1-50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA sequencing of Escherichia coli: bottleneck relief line 1, day 50</TITLE>
    <STUDY_REF accession="SRP105908">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105908</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA385021</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Samples were streaked to single colonies on LB agar. Single colonies were then used to inoculate LB liquid media. Genomic DNA was isolated using the Wizard Genomic DNA Purification Kit (Promega), and quantified using the Nanodrop 1000 Spectrophotometer and Qubit 2.0 Fluorometer. Sequencing was carried out by Macrogen Korea using an Illumina MiSeq platform with 2x250bp paired end reads. All 15 evolved samples were multiplexed in a single Illumina MiSeq Lane.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2158109">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2158109</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|nwheeler443">BR1-50</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>BR1-50</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2774801" alias="BN1-50">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2774801</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2620010">BN1-50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA sequencing of Escherichia coli: bottleneck line 1, day 50</TITLE>
    <STUDY_REF accession="SRP105908">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105908</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA385021</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Samples were streaked to single colonies on LB agar. Single colonies were then used to inoculate LB liquid media. Genomic DNA was isolated using the Wizard Genomic DNA Purification Kit (Promega), and quantified using the Nanodrop 1000 Spectrophotometer and Qubit 2.0 Fluorometer. Sequencing was carried out by Macrogen Korea using an Illumina MiSeq platform with 2x250bp paired end reads. All 15 evolved samples were multiplexed in a single Illumina MiSeq Lane.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2158111">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2158111</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|nwheeler443">BN1-50</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>BN1-50</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2774802" alias="BNC5-100">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2774802</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2620010">BNC5-100</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA sequencing of Escherichia coli: bottleneck control line 5, day 100</TITLE>
    <STUDY_REF accession="SRP105908">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105908</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA385021</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Samples were streaked to single colonies on LB agar. Single colonies were then used to inoculate LB liquid media. Genomic DNA was isolated using the Wizard Genomic DNA Purification Kit (Promega), and quantified using the Nanodrop 1000 Spectrophotometer and Qubit 2.0 Fluorometer. Sequencing was carried out by Macrogen Korea using an Illumina MiSeq platform with 2x250bp paired end reads. All 15 evolved samples were multiplexed in a single Illumina MiSeq Lane.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2158112">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2158112</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|nwheeler443">BNC5-100</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>BNC5-100</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2774803" alias="BNC4-100">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2774803</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2620010">BNC4-100</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA sequencing of Escherichia coli: bottleneck control line 4, day 100</TITLE>
    <STUDY_REF accession="SRP105908">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105908</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA385021</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Samples were streaked to single colonies on LB agar. Single colonies were then used to inoculate LB liquid media. Genomic DNA was isolated using the Wizard Genomic DNA Purification Kit (Promega), and quantified using the Nanodrop 1000 Spectrophotometer and Qubit 2.0 Fluorometer. Sequencing was carried out by Macrogen Korea using an Illumina MiSeq platform with 2x250bp paired end reads. All 15 evolved samples were multiplexed in a single Illumina MiSeq Lane.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2158113">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2158113</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|nwheeler443">BNC4-100</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>BNC4-100</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2774804" alias="BNC3-100">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2774804</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2620010">BNC3-100</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA sequencing of Escherichia coli: bottleneck control line 3, day 100</TITLE>
    <STUDY_REF accession="SRP105908">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105908</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA385021</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Samples were streaked to single colonies on LB agar. Single colonies were then used to inoculate LB liquid media. Genomic DNA was isolated using the Wizard Genomic DNA Purification Kit (Promega), and quantified using the Nanodrop 1000 Spectrophotometer and Qubit 2.0 Fluorometer. Sequencing was carried out by Macrogen Korea using an Illumina MiSeq platform with 2x250bp paired end reads. All 15 evolved samples were multiplexed in a single Illumina MiSeq Lane.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2158116">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2158116</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|nwheeler443">BNC3-100</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>BNC3-100</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2774805" alias="BNC2-100">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2774805</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2620010">BNC2-100</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA sequencing of Escherichia coli: bottleneck control line 2, day 100</TITLE>
    <STUDY_REF accession="SRP105908">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105908</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA385021</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Samples were streaked to single colonies on LB agar. Single colonies were then used to inoculate LB liquid media. Genomic DNA was isolated using the Wizard Genomic DNA Purification Kit (Promega), and quantified using the Nanodrop 1000 Spectrophotometer and Qubit 2.0 Fluorometer. Sequencing was carried out by Macrogen Korea using an Illumina MiSeq platform with 2x250bp paired end reads. All 15 evolved samples were multiplexed in a single Illumina MiSeq Lane.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2158114">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2158114</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|nwheeler443">BNC2-100</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>BNC2-100</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2774806" alias="BNC1-100">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2774806</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2620010">BNC1-100</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA sequencing of Escherichia coli: bottleneck control line 1, day 100</TITLE>
    <STUDY_REF accession="SRP105908">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105908</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA385021</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Samples were streaked to single colonies on LB agar. Single colonies were then used to inoculate LB liquid media. Genomic DNA was isolated using the Wizard Genomic DNA Purification Kit (Promega), and quantified using the Nanodrop 1000 Spectrophotometer and Qubit 2.0 Fluorometer. Sequencing was carried out by Macrogen Korea using an Illumina MiSeq platform with 2x250bp paired end reads. All 15 evolved samples were multiplexed in a single Illumina MiSeq Lane.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2158115">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2158115</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|nwheeler443">BNC1-100</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>BNC1-100</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2774807" alias="BN10-100">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2774807</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2620010">BN10-100</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA sequencing of Escherichia coli: bottleneck line 10, day 100</TITLE>
    <STUDY_REF accession="SRP105908">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105908</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA385021</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Samples were streaked to single colonies on LB agar. Single colonies were then used to inoculate LB liquid media. Genomic DNA was isolated using the Wizard Genomic DNA Purification Kit (Promega), and quantified using the Nanodrop 1000 Spectrophotometer and Qubit 2.0 Fluorometer. Sequencing was carried out by Macrogen Korea using an Illumina MiSeq platform with 2x250bp paired end reads. All 15 evolved samples were multiplexed in a single Illumina MiSeq Lane.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2158117">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2158117</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|nwheeler443">BN10-100</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>BN10-100</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2774808" alias="BN9-100">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2774808</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2620010">BN9-100</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA sequencing of Escherichia coli: bottleneck line 9, day 100</TITLE>
    <STUDY_REF accession="SRP105908">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105908</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA385021</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Samples were streaked to single colonies on LB agar. Single colonies were then used to inoculate LB liquid media. Genomic DNA was isolated using the Wizard Genomic DNA Purification Kit (Promega), and quantified using the Nanodrop 1000 Spectrophotometer and Qubit 2.0 Fluorometer. Sequencing was carried out by Macrogen Korea using an Illumina MiSeq platform with 2x250bp paired end reads. All 15 evolved samples were multiplexed in a single Illumina MiSeq Lane.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2158118">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2158118</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|nwheeler443">BN9-100</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>BN9-100</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2774809" alias="BN8-100">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2774809</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2620010">BN8-100</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA sequencing of Escherichia coli: bottleneck line 8, day 100</TITLE>
    <STUDY_REF accession="SRP105908">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105908</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA385021</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Samples were streaked to single colonies on LB agar. Single colonies were then used to inoculate LB liquid media. Genomic DNA was isolated using the Wizard Genomic DNA Purification Kit (Promega), and quantified using the Nanodrop 1000 Spectrophotometer and Qubit 2.0 Fluorometer. Sequencing was carried out by Macrogen Korea using an Illumina MiSeq platform with 2x250bp paired end reads. All 15 evolved samples were multiplexed in a single Illumina MiSeq Lane.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2158119">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2158119</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|nwheeler443">BN8-100</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>BN8-100</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2774810" alias="BN7-100">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2774810</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2620010">BN7-100</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA sequencing of Escherichia coli: bottleneck line 7, day 100</TITLE>
    <STUDY_REF accession="SRP105908">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105908</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA385021</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Samples were streaked to single colonies on LB agar. Single colonies were then used to inoculate LB liquid media. Genomic DNA was isolated using the Wizard Genomic DNA Purification Kit (Promega), and quantified using the Nanodrop 1000 Spectrophotometer and Qubit 2.0 Fluorometer. Sequencing was carried out by Macrogen Korea using an Illumina MiSeq platform with 2x250bp paired end reads. All 15 evolved samples were multiplexed in a single Illumina MiSeq Lane.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2158120">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2158120</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|nwheeler443">BN7-100</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>BN7-100</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2774811" alias="BN6-100">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2774811</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2620010">BN6-100</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA sequencing of Escherichia coli: bottleneck line 6, day 100</TITLE>
    <STUDY_REF accession="SRP105908">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105908</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA385021</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Samples were streaked to single colonies on LB agar. Single colonies were then used to inoculate LB liquid media. Genomic DNA was isolated using the Wizard Genomic DNA Purification Kit (Promega), and quantified using the Nanodrop 1000 Spectrophotometer and Qubit 2.0 Fluorometer. Sequencing was carried out by Macrogen Korea using an Illumina MiSeq platform with 2x250bp paired end reads. All 15 evolved samples were multiplexed in a single Illumina MiSeq Lane.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2158121">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2158121</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|nwheeler443">BN6-100</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>BN6-100</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2774812" alias="BN5-100">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2774812</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2620010">BN5-100</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA sequencing of Escherichia coli: bottleneck line 5, day 100</TITLE>
    <STUDY_REF accession="SRP105908">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105908</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA385021</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Samples were streaked to single colonies on LB agar. Single colonies were then used to inoculate LB liquid media. Genomic DNA was isolated using the Wizard Genomic DNA Purification Kit (Promega), and quantified using the Nanodrop 1000 Spectrophotometer and Qubit 2.0 Fluorometer. Sequencing was carried out by Macrogen Korea using an Illumina MiSeq platform with 2x250bp paired end reads. All 15 evolved samples were multiplexed in a single Illumina MiSeq Lane.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2158122">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2158122</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|nwheeler443">BN5-100</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>BN5-100</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2774813" alias="BN4-100">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2774813</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2620010">BN4-100</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA sequencing of Escherichia coli: bottleneck line 4, day 100</TITLE>
    <STUDY_REF accession="SRP105908">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105908</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA385021</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Samples were streaked to single colonies on LB agar. Single colonies were then used to inoculate LB liquid media. Genomic DNA was isolated using the Wizard Genomic DNA Purification Kit (Promega), and quantified using the Nanodrop 1000 Spectrophotometer and Qubit 2.0 Fluorometer. Sequencing was carried out by Macrogen Korea using an Illumina MiSeq platform with 2x250bp paired end reads. All 15 evolved samples were multiplexed in a single Illumina MiSeq Lane.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2158123">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2158123</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|nwheeler443">BN4-100</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>BN4-100</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2774814" alias="BN3-100">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2774814</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2620010">BN3-100</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA sequencing of Escherichia coli: bottleneck line 3, day 100</TITLE>
    <STUDY_REF accession="SRP105908">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105908</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA385021</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Samples were streaked to single colonies on LB agar. Single colonies were then used to inoculate LB liquid media. Genomic DNA was isolated using the Wizard Genomic DNA Purification Kit (Promega), and quantified using the Nanodrop 1000 Spectrophotometer and Qubit 2.0 Fluorometer. Sequencing was carried out by Macrogen Korea using an Illumina MiSeq platform with 2x250bp paired end reads. All 15 evolved samples were multiplexed in a single Illumina MiSeq Lane.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2158124">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2158124</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|nwheeler443">BN3-100</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>BN3-100</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2774815" alias="BN2-100">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2774815</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2620010">BN2-100</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA sequencing of Escherichia coli: bottleneck line 2, day 100</TITLE>
    <STUDY_REF accession="SRP105908">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105908</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA385021</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Samples were streaked to single colonies on LB agar. Single colonies were then used to inoculate LB liquid media. Genomic DNA was isolated using the Wizard Genomic DNA Purification Kit (Promega), and quantified using the Nanodrop 1000 Spectrophotometer and Qubit 2.0 Fluorometer. Sequencing was carried out by Macrogen Korea using an Illumina MiSeq platform with 2x250bp paired end reads. All 15 evolved samples were multiplexed in a single Illumina MiSeq Lane.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2158125">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2158125</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|nwheeler443">BN2-100</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>BN2-100</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2774816" alias="BN1-100">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2774816</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2620010">BN1-100</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA sequencing of Escherichia coli: bottleneck line 1, day 100</TITLE>
    <STUDY_REF accession="SRP105908">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105908</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA385021</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Samples were streaked to single colonies on LB agar. Single colonies were then used to inoculate LB liquid media. Genomic DNA was isolated using the Wizard Genomic DNA Purification Kit (Promega), and quantified using the Nanodrop 1000 Spectrophotometer and Qubit 2.0 Fluorometer. Sequencing was carried out by Macrogen Korea using an Illumina MiSeq platform with 2x250bp paired end reads. All 15 evolved samples were multiplexed in a single Illumina MiSeq Lane.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2158126">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2158126</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|nwheeler443">BN1-100</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>BN1-100</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2774817" alias="Ancestor">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2774817</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2620010">Ancestor</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA sequencing of Escherichia coli: day 0 ancestral isolate</TITLE>
    <STUDY_REF accession="SRP105908">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105908</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA385021</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Samples were streaked to single colonies on LB agar. Single colonies were then used to inoculate LB liquid media. Genomic DNA was isolated using the Wizard Genomic DNA Purification Kit (Promega), and quantified using the Nanodrop 1000 Spectrophotometer and Qubit 2.0 Fluorometer. Sequencing was carried out by Macrogen Korea using an Illumina MiSeq platform with 2x250bp paired end reads. All 15 evolved samples were multiplexed in a single Illumina MiSeq Lane.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2158127">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2158127</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|nwheeler443">Ancestor</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Ancestor</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
