<?xml version="1.0" encoding="UTF-8" standalone="yes"?>
<SAMPLE_SET>
    <SAMPLE alias="DRS092476" center_name="UTGSFSCB-ML" accession="DRS092476">
        <IDENTIFIERS>
            <PRIMARY_ID label="BioSample ID">SAMD00030053</PRIMARY_ID>
        </IDENTIFIERS>
        <SAMPLE_NAME>
            <TAXON_ID>85962</TAXON_ID>
            <SCIENTIFIC_NAME>Helicobacter pylori 26695</SCIENTIFIC_NAME>
        </SAMPLE_NAME>
        <SAMPLE_ATTRIBUTES>
            <SAMPLE_ATTRIBUTE>
                <TAG>description</TAG>
                <VALUE>wild-type. Exponential phase. strand-nonspecific mRNA-seq. This strain was grown in Brucella both containing 10% FBS up to mid-exponential phase (O.D.600 =0.4). Then, cells were harvested for RNA extraction. Total RNA was extracted from cell pellets using PureLink RNA mini kit (Ambion). rRNA was depleted using Ribo-Zero rRNA Removal kit for Gram-negative bacteria (Epicentre). cDNA library was constructed using TruSeq RNA library prep kit (Illumina). The indexed cDNA libraries were pooled and sequenced in HiSeq2500 platform (Illumina).</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>bioproject_id</TAG>
                <VALUE>PRJDB3908</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_name</TAG>
                <VALUE>26695_exp</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>strain</TAG>
                <VALUE>26695</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_title</TAG>
                <VALUE>26695_exp</VALUE>
            </SAMPLE_ATTRIBUTE>
        </SAMPLE_ATTRIBUTES>
    </SAMPLE>
    <SAMPLE alias="DRS092477" center_name="UTGSFSCB-ML" accession="DRS092477">
        <IDENTIFIERS>
            <PRIMARY_ID label="BioSample ID">SAMD00030054</PRIMARY_ID>
        </IDENTIFIERS>
        <SAMPLE_NAME>
            <TAXON_ID>85962</TAXON_ID>
            <SCIENTIFIC_NAME>Helicobacter pylori 26695</SCIENTIFIC_NAME>
        </SAMPLE_NAME>
        <SAMPLE_ATTRIBUTES>
            <SAMPLE_ATTRIBUTE>
                <TAG>description</TAG>
                <VALUE>PIK14  (deltaHP_0260::aphA) were 26695 derivative strains. Exponential phase. strand-nonspecific mRNA-seq. This strain was grown in Brucella both containing 10% FBS up to mid-exponential phase (O.D.600 =0.4). Then, cells were harvested for RNA extraction. Total RNA was extracted from cell pellets using PureLink RNA mini kit (Ambion). rRNA was depleted using Ribo-Zero rRNA Removal kit for Gram-negative bacteria (Epicentre). cDNA library was constructed using TruSeq RNA library prep kit (Illumina). The indexed cDNA libraries were pooled and sequenced in HiSeq2500 platform (Illumina).</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>bioproject_id</TAG>
                <VALUE>PRJDB3908</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_name</TAG>
                <VALUE>PIK14_exp</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>strain</TAG>
                <VALUE>26695</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sub_strain</TAG>
                <VALUE>PIK14</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_title</TAG>
                <VALUE>PIK14_exp</VALUE>
            </SAMPLE_ATTRIBUTE>
        </SAMPLE_ATTRIBUTES>
    </SAMPLE>
    <SAMPLE alias="DRS092478" center_name="UTGSFSCB-ML" accession="DRS092478">
        <IDENTIFIERS>
            <PRIMARY_ID label="BioSample ID">SAMD00030055</PRIMARY_ID>
        </IDENTIFIERS>
        <SAMPLE_NAME>
            <TAXON_ID>85962</TAXON_ID>
            <SCIENTIFIC_NAME>Helicobacter pylori 26695</SCIENTIFIC_NAME>
        </SAMPLE_NAME>
        <SAMPLE_ATTRIBUTES>
            <SAMPLE_ATTRIBUTE>
                <TAG>description</TAG>
                <VALUE>PIK16 (deltaHP_0593::aphA) were 26695 derivative strains. Exponential phase. strand-nonspecific mRNA-seq. This strain was grown in Brucella both containing 10% FBS up to mid-exponential phase (O.D.600 =0.4). Then, cells were harvested for RNA extraction. Total RNA was extracted from cell pellets using PureLink RNA mini kit (Ambion). rRNA was depleted using Ribo-Zero rRNA Removal kit for Gram-negative bacteria (Epicentre). cDNA library was constructed using TruSeq RNA library prep kit (Illumina). The indexed cDNA libraries were pooled and sequenced in HiSeq2500 platform (Illumina).</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>bioproject_id</TAG>
                <VALUE>PRJDB3908</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_name</TAG>
                <VALUE>PIK16_exp</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>strain</TAG>
                <VALUE>26695</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sub_strain</TAG>
                <VALUE>PIK16</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_title</TAG>
                <VALUE>PIK16_exp</VALUE>
            </SAMPLE_ATTRIBUTE>
        </SAMPLE_ATTRIBUTES>
    </SAMPLE>
    <SAMPLE alias="DRS092479" center_name="UTGSFSCB-ML" accession="DRS092479">
        <IDENTIFIERS>
            <PRIMARY_ID label="BioSample ID">SAMD00030056</PRIMARY_ID>
        </IDENTIFIERS>
        <SAMPLE_NAME>
            <TAXON_ID>85962</TAXON_ID>
            <SCIENTIFIC_NAME>Helicobacter pylori 26695</SCIENTIFIC_NAME>
        </SAMPLE_NAME>
        <SAMPLE_ATTRIBUTES>
            <SAMPLE_ATTRIBUTE>
                <TAG>description</TAG>
                <VALUE>PIK17 (deltaHP_0790::aphA) were 26695 derivative strains. Exponential phase. strand-nonspecific mRNA-seq. This strain was grown in Brucella both containing 10% FBS up to mid-exponential phase (O.D.600 =0.4). Then, cells were harvested for RNA extraction. Total RNA was extracted from cell pellets using PureLink RNA mini kit (Ambion). rRNA was depleted using Ribo-Zero rRNA Removal kit for Gram-negative bacteria (Epicentre). cDNA library was constructed using TruSeq RNA library prep kit (Illumina). The indexed cDNA libraries were pooled and sequenced in HiSeq2500 platform (Illumina).</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>bioproject_id</TAG>
                <VALUE>PRJDB3908</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_name</TAG>
                <VALUE>PIK17_exp</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>strain</TAG>
                <VALUE>26695</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sub_strain</TAG>
                <VALUE>PIK17</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_title</TAG>
                <VALUE>PIK17_exp</VALUE>
            </SAMPLE_ATTRIBUTE>
        </SAMPLE_ATTRIBUTES>
    </SAMPLE>
</SAMPLE_SET>
