<?xml version="1.0" encoding="UTF-8" standalone="yes"?>
<STUDY_SET>
    <STUDY alias="DRP005266" center_name="UT_COB" accession="DRP005266">
        <IDENTIFIERS>
            <PRIMARY_ID label="BioProject ID">PRJDB5943</PRIMARY_ID>
        </IDENTIFIERS>
        <DESCRIPTOR>
            <STUDY_TITLE>Gut microbiota of a number of Drosophila mutant strains and insects</STUDY_TITLE>
            <STUDY_TYPE existing_study_type="Other"/>
            <STUDY_ABSTRACT>Whole fly samples of a number of mutant strains, mainly related to innate immunity, of Drosophila adults and larvae were used. The 16S rRNA gene hypervariable V1-V2 regions were PCR-amplified using universal primers (a barcoded 27Fmod and 338R) and, multiplexed amplicon pyrosequencing was carried out using MiSeq (illumina).</STUDY_ABSTRACT>
            <CENTER_PROJECT_NAME>Gut microbiota of a number of Drosophila mutant strains and insects</CENTER_PROJECT_NAME>
            <RELATED_STUDIES>
                <RELATED_STUDY>
                    <RELATED_LINK>
                        <DB>bioproject</DB>
                        <ID>PRJDB5943</ID>
                        <LABEL>PRJDB5943</LABEL>
                    </RELATED_LINK>
                    <IS_PRIMARY>true</IS_PRIMARY>
                </RELATED_STUDY>
            </RELATED_STUDIES>
            <STUDY_DESCRIPTION>Whole fly samples of a number of mutant strains, mainly related to innate immunity, of Drosophila adults and larvae were used. The 16S rRNA gene hypervariable V1-V2 regions were PCR-amplified using universal primers (a barcoded 27Fmod and 338R) and, multiplexed amplicon pyrosequencing was carried out using MiSeq (illumina).</STUDY_DESCRIPTION>
        </DESCRIPTOR>
    </STUDY>
</STUDY_SET>
