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<EXPERIMENT_SET>
    <EXPERIMENT alias="DRX024426" center_name="NIBB" accession="DRX024426">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022978</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033620" refcenter="NIBB" accession="DRS033620">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022978</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024427" center_name="NIBB" accession="DRX024427">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022978</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033620" refcenter="NIBB" accession="DRS033620">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022978</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024428" center_name="NIBB" accession="DRX024428">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023087</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033729" refcenter="NIBB" accession="DRS033729">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023087</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024429" center_name="NIBB" accession="DRX024429">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023087</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033729" refcenter="NIBB" accession="DRS033729">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023087</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024430" center_name="NIBB" accession="DRX024430">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023108</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033750" refcenter="NIBB" accession="DRS033750">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023108</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024431" center_name="NIBB" accession="DRX024431">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023108</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033750" refcenter="NIBB" accession="DRS033750">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023108</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024432" center_name="NIBB" accession="DRX024432">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023119</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033761" refcenter="NIBB" accession="DRS033761">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023119</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024433" center_name="NIBB" accession="DRX024433">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023119</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033761" refcenter="NIBB" accession="DRS033761">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023119</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024434" center_name="NIBB" accession="DRX024434">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023130</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033772" refcenter="NIBB" accession="DRS033772">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023130</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024435" center_name="NIBB" accession="DRX024435">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023130</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033772" refcenter="NIBB" accession="DRS033772">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023130</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024436" center_name="NIBB" accession="DRX024436">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023141</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033783" refcenter="NIBB" accession="DRS033783">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023141</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024437" center_name="NIBB" accession="DRX024437">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023141</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033783" refcenter="NIBB" accession="DRS033783">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023141</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024438" center_name="NIBB" accession="DRX024438">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023152</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033794" refcenter="NIBB" accession="DRS033794">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023152</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024439" center_name="NIBB" accession="DRX024439">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023152</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033794" refcenter="NIBB" accession="DRS033794">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023152</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024440" center_name="NIBB" accession="DRX024440">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023163</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033805" refcenter="NIBB" accession="DRS033805">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023163</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024441" center_name="NIBB" accession="DRX024441">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023163</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033805" refcenter="NIBB" accession="DRS033805">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023163</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024442" center_name="NIBB" accession="DRX024442">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023174</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033816" refcenter="NIBB" accession="DRS033816">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023174</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024443" center_name="NIBB" accession="DRX024443">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023174</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033816" refcenter="NIBB" accession="DRS033816">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023174</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024444" center_name="NIBB" accession="DRX024444">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022979</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033621" refcenter="NIBB" accession="DRS033621">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022979</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024445" center_name="NIBB" accession="DRX024445">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022979</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033621" refcenter="NIBB" accession="DRS033621">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022979</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024446" center_name="NIBB" accession="DRX024446">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022990</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033632" refcenter="NIBB" accession="DRS033632">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022990</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024447" center_name="NIBB" accession="DRX024447">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022990</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033632" refcenter="NIBB" accession="DRS033632">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022990</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024448" center_name="NIBB" accession="DRX024448">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023001</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033643" refcenter="NIBB" accession="DRS033643">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023001</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024449" center_name="NIBB" accession="DRX024449">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023001</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033643" refcenter="NIBB" accession="DRS033643">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023001</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024450" center_name="NIBB" accession="DRX024450">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023012</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033654" refcenter="NIBB" accession="DRS033654">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023012</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024451" center_name="NIBB" accession="DRX024451">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023012</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033654" refcenter="NIBB" accession="DRS033654">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023012</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024452" center_name="NIBB" accession="DRX024452">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023023</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033665" refcenter="NIBB" accession="DRS033665">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023023</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024453" center_name="NIBB" accession="DRX024453">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023023</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033665" refcenter="NIBB" accession="DRS033665">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023023</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024454" center_name="NIBB" accession="DRX024454">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023034</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033676" refcenter="NIBB" accession="DRS033676">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023034</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024455" center_name="NIBB" accession="DRX024455">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023034</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033676" refcenter="NIBB" accession="DRS033676">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023034</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024456" center_name="NIBB" accession="DRX024456">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023043</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033685" refcenter="NIBB" accession="DRS033685">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023043</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024457" center_name="NIBB" accession="DRX024457">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023043</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033685" refcenter="NIBB" accession="DRS033685">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023043</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024458" center_name="NIBB" accession="DRX024458">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023054</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033696" refcenter="NIBB" accession="DRS033696">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023054</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024459" center_name="NIBB" accession="DRX024459">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023054</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033696" refcenter="NIBB" accession="DRS033696">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023054</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024460" center_name="NIBB" accession="DRX024460">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023065</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033707" refcenter="NIBB" accession="DRS033707">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023065</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024461" center_name="NIBB" accession="DRX024461">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023065</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033707" refcenter="NIBB" accession="DRS033707">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023065</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024462" center_name="NIBB" accession="DRX024462">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023076</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033718" refcenter="NIBB" accession="DRS033718">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023076</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024463" center_name="NIBB" accession="DRX024463">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023076</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033718" refcenter="NIBB" accession="DRS033718">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023076</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024464" center_name="NIBB" accession="DRX024464">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023088</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033730" refcenter="NIBB" accession="DRS033730">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023088</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024465" center_name="NIBB" accession="DRX024465">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023088</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033730" refcenter="NIBB" accession="DRS033730">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023088</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024466" center_name="NIBB" accession="DRX024466">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023098</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033740" refcenter="NIBB" accession="DRS033740">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023098</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024467" center_name="NIBB" accession="DRX024467">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023098</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033740" refcenter="NIBB" accession="DRS033740">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023098</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024468" center_name="NIBB" accession="DRX024468">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023100</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033742" refcenter="NIBB" accession="DRS033742">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023100</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024469" center_name="NIBB" accession="DRX024469">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023100</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033742" refcenter="NIBB" accession="DRS033742">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023100</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024470" center_name="NIBB" accession="DRX024470">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023101</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033743" refcenter="NIBB" accession="DRS033743">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023101</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024471" center_name="NIBB" accession="DRX024471">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023101</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033743" refcenter="NIBB" accession="DRS033743">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023101</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024472" center_name="NIBB" accession="DRX024472">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023102</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033744" refcenter="NIBB" accession="DRS033744">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023102</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024473" center_name="NIBB" accession="DRX024473">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023102</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033744" refcenter="NIBB" accession="DRS033744">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023102</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024474" center_name="NIBB" accession="DRX024474">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023103</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033745" refcenter="NIBB" accession="DRS033745">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023103</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024475" center_name="NIBB" accession="DRX024475">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023103</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033745" refcenter="NIBB" accession="DRS033745">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023103</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024476" center_name="NIBB" accession="DRX024476">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023104</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033746" refcenter="NIBB" accession="DRS033746">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023104</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024477" center_name="NIBB" accession="DRX024477">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023104</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033746" refcenter="NIBB" accession="DRS033746">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023104</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024478" center_name="NIBB" accession="DRX024478">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023105</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033747" refcenter="NIBB" accession="DRS033747">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023105</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024479" center_name="NIBB" accession="DRX024479">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023105</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033747" refcenter="NIBB" accession="DRS033747">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023105</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024480" center_name="NIBB" accession="DRX024480">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023106</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033748" refcenter="NIBB" accession="DRS033748">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023106</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024481" center_name="NIBB" accession="DRX024481">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023106</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033748" refcenter="NIBB" accession="DRS033748">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023106</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024482" center_name="NIBB" accession="DRX024482">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023107</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033749" refcenter="NIBB" accession="DRS033749">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023107</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024483" center_name="NIBB" accession="DRX024483">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023107</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033749" refcenter="NIBB" accession="DRS033749">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023107</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024484" center_name="NIBB" accession="DRX024484">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023109</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033751" refcenter="NIBB" accession="DRS033751">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023109</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024485" center_name="NIBB" accession="DRX024485">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023109</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033751" refcenter="NIBB" accession="DRS033751">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023109</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024486" center_name="NIBB" accession="DRX024486">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023110</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033752" refcenter="NIBB" accession="DRS033752">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023110</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024487" center_name="NIBB" accession="DRX024487">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023110</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033752" refcenter="NIBB" accession="DRS033752">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023110</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024488" center_name="NIBB" accession="DRX024488">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023111</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033753" refcenter="NIBB" accession="DRS033753">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023111</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024489" center_name="NIBB" accession="DRX024489">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023111</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033753" refcenter="NIBB" accession="DRS033753">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023111</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024490" center_name="NIBB" accession="DRX024490">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023112</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033754" refcenter="NIBB" accession="DRS033754">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023112</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024491" center_name="NIBB" accession="DRX024491">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023112</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033754" refcenter="NIBB" accession="DRS033754">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023112</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024492" center_name="NIBB" accession="DRX024492">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023113</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033755" refcenter="NIBB" accession="DRS033755">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023113</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024493" center_name="NIBB" accession="DRX024493">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023113</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033755" refcenter="NIBB" accession="DRS033755">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023113</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024494" center_name="NIBB" accession="DRX024494">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023114</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033756" refcenter="NIBB" accession="DRS033756">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023114</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024495" center_name="NIBB" accession="DRX024495">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023114</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033756" refcenter="NIBB" accession="DRS033756">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023114</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024496" center_name="NIBB" accession="DRX024496">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023115</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033757" refcenter="NIBB" accession="DRS033757">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023115</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024497" center_name="NIBB" accession="DRX024497">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023115</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033757" refcenter="NIBB" accession="DRS033757">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023115</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024498" center_name="NIBB" accession="DRX024498">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023116</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033758" refcenter="NIBB" accession="DRS033758">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023116</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024499" center_name="NIBB" accession="DRX024499">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023116</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033758" refcenter="NIBB" accession="DRS033758">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023116</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024500" center_name="NIBB" accession="DRX024500">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023117</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033759" refcenter="NIBB" accession="DRS033759">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023117</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024501" center_name="NIBB" accession="DRX024501">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023117</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033759" refcenter="NIBB" accession="DRS033759">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023117</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024502" center_name="NIBB" accession="DRX024502">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023118</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033760" refcenter="NIBB" accession="DRS033760">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023118</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024503" center_name="NIBB" accession="DRX024503">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023118</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033760" refcenter="NIBB" accession="DRS033760">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023118</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024504" center_name="NIBB" accession="DRX024504">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023120</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033762" refcenter="NIBB" accession="DRS033762">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023120</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024505" center_name="NIBB" accession="DRX024505">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023120</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033762" refcenter="NIBB" accession="DRS033762">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023120</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024506" center_name="NIBB" accession="DRX024506">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023121</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033763" refcenter="NIBB" accession="DRS033763">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023121</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024507" center_name="NIBB" accession="DRX024507">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023121</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033763" refcenter="NIBB" accession="DRS033763">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023121</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024508" center_name="NIBB" accession="DRX024508">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023122</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033764" refcenter="NIBB" accession="DRS033764">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023122</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024509" center_name="NIBB" accession="DRX024509">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023122</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033764" refcenter="NIBB" accession="DRS033764">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023122</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024510" center_name="NIBB" accession="DRX024510">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023123</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033765" refcenter="NIBB" accession="DRS033765">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023123</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024511" center_name="NIBB" accession="DRX024511">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023123</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033765" refcenter="NIBB" accession="DRS033765">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023123</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024512" center_name="NIBB" accession="DRX024512">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023124</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033766" refcenter="NIBB" accession="DRS033766">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023124</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024513" center_name="NIBB" accession="DRX024513">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023124</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033766" refcenter="NIBB" accession="DRS033766">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023124</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024514" center_name="NIBB" accession="DRX024514">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023125</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033767" refcenter="NIBB" accession="DRS033767">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023125</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024515" center_name="NIBB" accession="DRX024515">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023125</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033767" refcenter="NIBB" accession="DRS033767">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023125</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024516" center_name="NIBB" accession="DRX024516">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023126</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033768" refcenter="NIBB" accession="DRS033768">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023126</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024517" center_name="NIBB" accession="DRX024517">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023126</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033768" refcenter="NIBB" accession="DRS033768">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023126</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024518" center_name="NIBB" accession="DRX024518">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023127</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033769" refcenter="NIBB" accession="DRS033769">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023127</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024519" center_name="NIBB" accession="DRX024519">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023127</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033769" refcenter="NIBB" accession="DRS033769">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023127</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024520" center_name="NIBB" accession="DRX024520">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023128</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033770" refcenter="NIBB" accession="DRS033770">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023128</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024521" center_name="NIBB" accession="DRX024521">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023128</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033770" refcenter="NIBB" accession="DRS033770">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023128</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024522" center_name="NIBB" accession="DRX024522">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023129</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033771" refcenter="NIBB" accession="DRS033771">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023129</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024523" center_name="NIBB" accession="DRX024523">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023129</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033771" refcenter="NIBB" accession="DRS033771">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023129</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024524" center_name="NIBB" accession="DRX024524">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023131</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033773" refcenter="NIBB" accession="DRS033773">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023131</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024525" center_name="NIBB" accession="DRX024525">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023131</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033773" refcenter="NIBB" accession="DRS033773">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023131</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024526" center_name="NIBB" accession="DRX024526">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023132</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033774" refcenter="NIBB" accession="DRS033774">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023132</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024527" center_name="NIBB" accession="DRX024527">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023132</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033774" refcenter="NIBB" accession="DRS033774">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023132</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024528" center_name="NIBB" accession="DRX024528">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023133</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033775" refcenter="NIBB" accession="DRS033775">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023133</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024529" center_name="NIBB" accession="DRX024529">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023133</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033775" refcenter="NIBB" accession="DRS033775">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023133</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024530" center_name="NIBB" accession="DRX024530">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023134</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033776" refcenter="NIBB" accession="DRS033776">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023134</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024531" center_name="NIBB" accession="DRX024531">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023134</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033776" refcenter="NIBB" accession="DRS033776">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023134</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024532" center_name="NIBB" accession="DRX024532">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023135</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033777" refcenter="NIBB" accession="DRS033777">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023135</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024533" center_name="NIBB" accession="DRX024533">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023135</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033777" refcenter="NIBB" accession="DRS033777">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023135</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024534" center_name="NIBB" accession="DRX024534">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023136</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033778" refcenter="NIBB" accession="DRS033778">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023136</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024535" center_name="NIBB" accession="DRX024535">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023136</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033778" refcenter="NIBB" accession="DRS033778">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023136</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024536" center_name="NIBB" accession="DRX024536">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023137</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033779" refcenter="NIBB" accession="DRS033779">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023137</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024537" center_name="NIBB" accession="DRX024537">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023137</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033779" refcenter="NIBB" accession="DRS033779">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023137</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024538" center_name="NIBB" accession="DRX024538">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023138</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033780" refcenter="NIBB" accession="DRS033780">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023138</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024539" center_name="NIBB" accession="DRX024539">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023138</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033780" refcenter="NIBB" accession="DRS033780">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023138</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024540" center_name="NIBB" accession="DRX024540">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023139</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033781" refcenter="NIBB" accession="DRS033781">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023139</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024541" center_name="NIBB" accession="DRX024541">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023139</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033781" refcenter="NIBB" accession="DRS033781">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023139</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024542" center_name="NIBB" accession="DRX024542">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023140</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033782" refcenter="NIBB" accession="DRS033782">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023140</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024543" center_name="NIBB" accession="DRX024543">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023140</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033782" refcenter="NIBB" accession="DRS033782">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023140</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024544" center_name="NIBB" accession="DRX024544">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023142</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033784" refcenter="NIBB" accession="DRS033784">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023142</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024545" center_name="NIBB" accession="DRX024545">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023142</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033784" refcenter="NIBB" accession="DRS033784">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023142</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024546" center_name="NIBB" accession="DRX024546">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023143</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033785" refcenter="NIBB" accession="DRS033785">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023143</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024547" center_name="NIBB" accession="DRX024547">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023143</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033785" refcenter="NIBB" accession="DRS033785">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023143</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024548" center_name="NIBB" accession="DRX024548">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023144</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033786" refcenter="NIBB" accession="DRS033786">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023144</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024549" center_name="NIBB" accession="DRX024549">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023144</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033786" refcenter="NIBB" accession="DRS033786">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023144</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024550" center_name="NIBB" accession="DRX024550">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023145</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033787" refcenter="NIBB" accession="DRS033787">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023145</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024551" center_name="NIBB" accession="DRX024551">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023145</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033787" refcenter="NIBB" accession="DRS033787">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023145</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024552" center_name="NIBB" accession="DRX024552">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023146</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033788" refcenter="NIBB" accession="DRS033788">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023146</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024553" center_name="NIBB" accession="DRX024553">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023146</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033788" refcenter="NIBB" accession="DRS033788">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023146</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024554" center_name="NIBB" accession="DRX024554">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023147</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033789" refcenter="NIBB" accession="DRS033789">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023147</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024555" center_name="NIBB" accession="DRX024555">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023147</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033789" refcenter="NIBB" accession="DRS033789">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023147</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024556" center_name="NIBB" accession="DRX024556">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023148</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033790" refcenter="NIBB" accession="DRS033790">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023148</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024557" center_name="NIBB" accession="DRX024557">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023148</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033790" refcenter="NIBB" accession="DRS033790">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023148</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024558" center_name="NIBB" accession="DRX024558">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023149</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033791" refcenter="NIBB" accession="DRS033791">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023149</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024559" center_name="NIBB" accession="DRX024559">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023149</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033791" refcenter="NIBB" accession="DRS033791">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023149</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024560" center_name="NIBB" accession="DRX024560">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023150</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033792" refcenter="NIBB" accession="DRS033792">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023150</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024561" center_name="NIBB" accession="DRX024561">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023150</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033792" refcenter="NIBB" accession="DRS033792">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023150</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024562" center_name="NIBB" accession="DRX024562">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023151</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033793" refcenter="NIBB" accession="DRS033793">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023151</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024563" center_name="NIBB" accession="DRX024563">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023151</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033793" refcenter="NIBB" accession="DRS033793">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023151</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024564" center_name="NIBB" accession="DRX024564">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023153</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033795" refcenter="NIBB" accession="DRS033795">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023153</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024565" center_name="NIBB" accession="DRX024565">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023153</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033795" refcenter="NIBB" accession="DRS033795">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023153</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024566" center_name="NIBB" accession="DRX024566">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023154</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033796" refcenter="NIBB" accession="DRS033796">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023154</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024567" center_name="NIBB" accession="DRX024567">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023154</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033796" refcenter="NIBB" accession="DRS033796">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023154</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024568" center_name="NIBB" accession="DRX024568">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023155</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033797" refcenter="NIBB" accession="DRS033797">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023155</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024569" center_name="NIBB" accession="DRX024569">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023155</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033797" refcenter="NIBB" accession="DRS033797">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023155</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024570" center_name="NIBB" accession="DRX024570">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023156</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033798" refcenter="NIBB" accession="DRS033798">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023156</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024571" center_name="NIBB" accession="DRX024571">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023156</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033798" refcenter="NIBB" accession="DRS033798">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023156</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024572" center_name="NIBB" accession="DRX024572">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023157</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033799" refcenter="NIBB" accession="DRS033799">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023157</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024573" center_name="NIBB" accession="DRX024573">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023157</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033799" refcenter="NIBB" accession="DRS033799">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023157</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024574" center_name="NIBB" accession="DRX024574">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023158</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033800" refcenter="NIBB" accession="DRS033800">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023158</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024575" center_name="NIBB" accession="DRX024575">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023158</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033800" refcenter="NIBB" accession="DRS033800">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023158</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024576" center_name="NIBB" accession="DRX024576">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023159</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033801" refcenter="NIBB" accession="DRS033801">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023159</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024577" center_name="NIBB" accession="DRX024577">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023159</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033801" refcenter="NIBB" accession="DRS033801">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023159</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024578" center_name="NIBB" accession="DRX024578">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023160</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033802" refcenter="NIBB" accession="DRS033802">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023160</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024579" center_name="NIBB" accession="DRX024579">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023160</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033802" refcenter="NIBB" accession="DRS033802">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023160</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024580" center_name="NIBB" accession="DRX024580">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023161</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033803" refcenter="NIBB" accession="DRS033803">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023161</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024581" center_name="NIBB" accession="DRX024581">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023161</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033803" refcenter="NIBB" accession="DRS033803">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023161</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024582" center_name="NIBB" accession="DRX024582">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023162</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033804" refcenter="NIBB" accession="DRS033804">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023162</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024583" center_name="NIBB" accession="DRX024583">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023162</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033804" refcenter="NIBB" accession="DRS033804">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023162</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024584" center_name="NIBB" accession="DRX024584">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023164</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033806" refcenter="NIBB" accession="DRS033806">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023164</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024585" center_name="NIBB" accession="DRX024585">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023164</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033806" refcenter="NIBB" accession="DRS033806">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023164</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024586" center_name="NIBB" accession="DRX024586">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023165</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033807" refcenter="NIBB" accession="DRS033807">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023165</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024587" center_name="NIBB" accession="DRX024587">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023165</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033807" refcenter="NIBB" accession="DRS033807">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023165</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024588" center_name="NIBB" accession="DRX024588">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023166</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033808" refcenter="NIBB" accession="DRS033808">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023166</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024589" center_name="NIBB" accession="DRX024589">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023166</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033808" refcenter="NIBB" accession="DRS033808">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023166</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024590" center_name="NIBB" accession="DRX024590">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023167</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033809" refcenter="NIBB" accession="DRS033809">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023167</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024591" center_name="NIBB" accession="DRX024591">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023167</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033809" refcenter="NIBB" accession="DRS033809">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023167</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024592" center_name="NIBB" accession="DRX024592">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023168</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033810" refcenter="NIBB" accession="DRS033810">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023168</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024593" center_name="NIBB" accession="DRX024593">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023168</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033810" refcenter="NIBB" accession="DRS033810">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023168</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024594" center_name="NIBB" accession="DRX024594">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023169</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033811" refcenter="NIBB" accession="DRS033811">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023169</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024595" center_name="NIBB" accession="DRX024595">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023169</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033811" refcenter="NIBB" accession="DRS033811">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023169</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024596" center_name="NIBB" accession="DRX024596">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023170</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033812" refcenter="NIBB" accession="DRS033812">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023170</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024597" center_name="NIBB" accession="DRX024597">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023170</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033812" refcenter="NIBB" accession="DRS033812">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023170</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024598" center_name="NIBB" accession="DRX024598">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023171</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033813" refcenter="NIBB" accession="DRS033813">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023171</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024599" center_name="NIBB" accession="DRX024599">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023171</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033813" refcenter="NIBB" accession="DRS033813">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023171</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024600" center_name="NIBB" accession="DRX024600">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023172</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033814" refcenter="NIBB" accession="DRS033814">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023172</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024601" center_name="NIBB" accession="DRX024601">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023172</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033814" refcenter="NIBB" accession="DRS033814">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023172</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024602" center_name="NIBB" accession="DRX024602">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023173</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033815" refcenter="NIBB" accession="DRS033815">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023173</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024603" center_name="NIBB" accession="DRX024603">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023173</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033815" refcenter="NIBB" accession="DRS033815">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023173</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024604" center_name="NIBB" accession="DRX024604">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023175</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033817" refcenter="NIBB" accession="DRS033817">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023175</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024605" center_name="NIBB" accession="DRX024605">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023175</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033817" refcenter="NIBB" accession="DRS033817">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023175</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024606" center_name="NIBB" accession="DRX024606">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023176</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033818" refcenter="NIBB" accession="DRS033818">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023176</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024607" center_name="NIBB" accession="DRX024607">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023176</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033818" refcenter="NIBB" accession="DRS033818">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023176</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024608" center_name="NIBB" accession="DRX024608">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023177</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033819" refcenter="NIBB" accession="DRS033819">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023177</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024609" center_name="NIBB" accession="DRX024609">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023177</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033819" refcenter="NIBB" accession="DRS033819">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023177</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024610" center_name="NIBB" accession="DRX024610">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023178</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033820" refcenter="NIBB" accession="DRS033820">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023178</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024611" center_name="NIBB" accession="DRX024611">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023178</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033820" refcenter="NIBB" accession="DRS033820">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023178</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024612" center_name="NIBB" accession="DRX024612">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023179</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033821" refcenter="NIBB" accession="DRS033821">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023179</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024613" center_name="NIBB" accession="DRX024613">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023179</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033821" refcenter="NIBB" accession="DRS033821">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023179</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024614" center_name="NIBB" accession="DRX024614">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023180</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033822" refcenter="NIBB" accession="DRS033822">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023180</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024615" center_name="NIBB" accession="DRX024615">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023180</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033822" refcenter="NIBB" accession="DRS033822">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023180</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024616" center_name="NIBB" accession="DRX024616">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023181</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033823" refcenter="NIBB" accession="DRS033823">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023181</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024617" center_name="NIBB" accession="DRX024617">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023181</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033823" refcenter="NIBB" accession="DRS033823">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023181</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024618" center_name="NIBB" accession="DRX024618">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023182</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033824" refcenter="NIBB" accession="DRS033824">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023182</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024619" center_name="NIBB" accession="DRX024619">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023182</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033824" refcenter="NIBB" accession="DRS033824">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023182</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024620" center_name="NIBB" accession="DRX024620">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023183</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033825" refcenter="NIBB" accession="DRS033825">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023183</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024621" center_name="NIBB" accession="DRX024621">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023183</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033825" refcenter="NIBB" accession="DRS033825">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023183</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024622" center_name="NIBB" accession="DRX024622">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023184</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033826" refcenter="NIBB" accession="DRS033826">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023184</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024623" center_name="NIBB" accession="DRX024623">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023184</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033826" refcenter="NIBB" accession="DRS033826">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023184</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024624" center_name="NIBB" accession="DRX024624">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022980</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033622" refcenter="NIBB" accession="DRS033622">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022980</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024625" center_name="NIBB" accession="DRX024625">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022980</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033622" refcenter="NIBB" accession="DRS033622">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022980</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024626" center_name="NIBB" accession="DRX024626">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022981</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033623" refcenter="NIBB" accession="DRS033623">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022981</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024627" center_name="NIBB" accession="DRX024627">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022981</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033623" refcenter="NIBB" accession="DRS033623">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022981</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024628" center_name="NIBB" accession="DRX024628">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022982</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033624" refcenter="NIBB" accession="DRS033624">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022982</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024629" center_name="NIBB" accession="DRX024629">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022982</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033624" refcenter="NIBB" accession="DRS033624">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022982</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024630" center_name="NIBB" accession="DRX024630">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022983</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033625" refcenter="NIBB" accession="DRS033625">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022983</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024631" center_name="NIBB" accession="DRX024631">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022983</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033625" refcenter="NIBB" accession="DRS033625">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022983</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024632" center_name="NIBB" accession="DRX024632">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022984</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033626" refcenter="NIBB" accession="DRS033626">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022984</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024633" center_name="NIBB" accession="DRX024633">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022984</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033626" refcenter="NIBB" accession="DRS033626">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022984</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024634" center_name="NIBB" accession="DRX024634">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022985</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033627" refcenter="NIBB" accession="DRS033627">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022985</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024635" center_name="NIBB" accession="DRX024635">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022985</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033627" refcenter="NIBB" accession="DRS033627">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022985</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024636" center_name="NIBB" accession="DRX024636">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022986</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033628" refcenter="NIBB" accession="DRS033628">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022986</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024637" center_name="NIBB" accession="DRX024637">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022986</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033628" refcenter="NIBB" accession="DRS033628">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022986</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024638" center_name="NIBB" accession="DRX024638">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022987</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033629" refcenter="NIBB" accession="DRS033629">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022987</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024639" center_name="NIBB" accession="DRX024639">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022987</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033629" refcenter="NIBB" accession="DRS033629">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022987</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024640" center_name="NIBB" accession="DRX024640">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022988</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033630" refcenter="NIBB" accession="DRS033630">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022988</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024641" center_name="NIBB" accession="DRX024641">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022988</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033630" refcenter="NIBB" accession="DRS033630">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022988</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024642" center_name="NIBB" accession="DRX024642">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022989</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033631" refcenter="NIBB" accession="DRS033631">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022989</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024643" center_name="NIBB" accession="DRX024643">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022989</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033631" refcenter="NIBB" accession="DRS033631">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022989</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024644" center_name="NIBB" accession="DRX024644">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022991</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033633" refcenter="NIBB" accession="DRS033633">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022991</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024645" center_name="NIBB" accession="DRX024645">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022991</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033633" refcenter="NIBB" accession="DRS033633">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022991</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024646" center_name="NIBB" accession="DRX024646">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022992</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033634" refcenter="NIBB" accession="DRS033634">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022992</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024647" center_name="NIBB" accession="DRX024647">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022992</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033634" refcenter="NIBB" accession="DRS033634">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022992</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024648" center_name="NIBB" accession="DRX024648">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022993</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033635" refcenter="NIBB" accession="DRS033635">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022993</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024649" center_name="NIBB" accession="DRX024649">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022993</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033635" refcenter="NIBB" accession="DRS033635">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022993</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024650" center_name="NIBB" accession="DRX024650">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022994</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033636" refcenter="NIBB" accession="DRS033636">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022994</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024651" center_name="NIBB" accession="DRX024651">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022994</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033636" refcenter="NIBB" accession="DRS033636">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022994</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024652" center_name="NIBB" accession="DRX024652">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022995</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033637" refcenter="NIBB" accession="DRS033637">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022995</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024653" center_name="NIBB" accession="DRX024653">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022995</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033637" refcenter="NIBB" accession="DRS033637">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022995</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024654" center_name="NIBB" accession="DRX024654">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022996</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033638" refcenter="NIBB" accession="DRS033638">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022996</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024655" center_name="NIBB" accession="DRX024655">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022996</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033638" refcenter="NIBB" accession="DRS033638">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022996</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024656" center_name="NIBB" accession="DRX024656">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022997</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033639" refcenter="NIBB" accession="DRS033639">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022997</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024657" center_name="NIBB" accession="DRX024657">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022997</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033639" refcenter="NIBB" accession="DRS033639">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022997</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024658" center_name="NIBB" accession="DRX024658">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022998</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033640" refcenter="NIBB" accession="DRS033640">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022998</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024659" center_name="NIBB" accession="DRX024659">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022998</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033640" refcenter="NIBB" accession="DRS033640">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022998</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024660" center_name="NIBB" accession="DRX024660">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022999</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033641" refcenter="NIBB" accession="DRS033641">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022999</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024661" center_name="NIBB" accession="DRX024661">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022999</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033641" refcenter="NIBB" accession="DRS033641">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022999</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024662" center_name="NIBB" accession="DRX024662">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023000</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033642" refcenter="NIBB" accession="DRS033642">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023000</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024663" center_name="NIBB" accession="DRX024663">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023000</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033642" refcenter="NIBB" accession="DRS033642">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023000</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024664" center_name="NIBB" accession="DRX024664">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023002</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033644" refcenter="NIBB" accession="DRS033644">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023002</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024665" center_name="NIBB" accession="DRX024665">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023002</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033644" refcenter="NIBB" accession="DRS033644">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023002</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024666" center_name="NIBB" accession="DRX024666">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023003</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033645" refcenter="NIBB" accession="DRS033645">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023003</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024667" center_name="NIBB" accession="DRX024667">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023003</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033645" refcenter="NIBB" accession="DRS033645">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023003</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024668" center_name="NIBB" accession="DRX024668">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023004</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033646" refcenter="NIBB" accession="DRS033646">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023004</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024669" center_name="NIBB" accession="DRX024669">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023004</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033646" refcenter="NIBB" accession="DRS033646">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023004</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024670" center_name="NIBB" accession="DRX024670">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023005</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033647" refcenter="NIBB" accession="DRS033647">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023005</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024671" center_name="NIBB" accession="DRX024671">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023005</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033647" refcenter="NIBB" accession="DRS033647">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023005</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024672" center_name="NIBB" accession="DRX024672">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023006</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033648" refcenter="NIBB" accession="DRS033648">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023006</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024673" center_name="NIBB" accession="DRX024673">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023006</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033648" refcenter="NIBB" accession="DRS033648">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023006</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024674" center_name="NIBB" accession="DRX024674">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023007</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033649" refcenter="NIBB" accession="DRS033649">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023007</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024675" center_name="NIBB" accession="DRX024675">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023007</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033649" refcenter="NIBB" accession="DRS033649">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023007</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024676" center_name="NIBB" accession="DRX024676">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023008</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033650" refcenter="NIBB" accession="DRS033650">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023008</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024677" center_name="NIBB" accession="DRX024677">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023008</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033650" refcenter="NIBB" accession="DRS033650">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023008</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024678" center_name="NIBB" accession="DRX024678">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023009</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033651" refcenter="NIBB" accession="DRS033651">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023009</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024679" center_name="NIBB" accession="DRX024679">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023009</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033651" refcenter="NIBB" accession="DRS033651">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023009</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024680" center_name="NIBB" accession="DRX024680">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023010</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033652" refcenter="NIBB" accession="DRS033652">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023010</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024681" center_name="NIBB" accession="DRX024681">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023010</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033652" refcenter="NIBB" accession="DRS033652">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023010</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024682" center_name="NIBB" accession="DRX024682">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023011</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033653" refcenter="NIBB" accession="DRS033653">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023011</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024683" center_name="NIBB" accession="DRX024683">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023011</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033653" refcenter="NIBB" accession="DRS033653">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023011</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024684" center_name="NIBB" accession="DRX024684">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023013</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033655" refcenter="NIBB" accession="DRS033655">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023013</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024685" center_name="NIBB" accession="DRX024685">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023013</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033655" refcenter="NIBB" accession="DRS033655">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023013</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024686" center_name="NIBB" accession="DRX024686">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023014</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033656" refcenter="NIBB" accession="DRS033656">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023014</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024687" center_name="NIBB" accession="DRX024687">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023014</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033656" refcenter="NIBB" accession="DRS033656">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023014</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024688" center_name="NIBB" accession="DRX024688">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023015</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033657" refcenter="NIBB" accession="DRS033657">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023015</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024689" center_name="NIBB" accession="DRX024689">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023015</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033657" refcenter="NIBB" accession="DRS033657">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023015</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024690" center_name="NIBB" accession="DRX024690">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023016</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033658" refcenter="NIBB" accession="DRS033658">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023016</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024691" center_name="NIBB" accession="DRX024691">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023016</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033658" refcenter="NIBB" accession="DRS033658">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023016</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024692" center_name="NIBB" accession="DRX024692">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023017</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033659" refcenter="NIBB" accession="DRS033659">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023017</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024693" center_name="NIBB" accession="DRX024693">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023017</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033659" refcenter="NIBB" accession="DRS033659">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023017</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024694" center_name="NIBB" accession="DRX024694">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023018</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033660" refcenter="NIBB" accession="DRS033660">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023018</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024695" center_name="NIBB" accession="DRX024695">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023018</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033660" refcenter="NIBB" accession="DRS033660">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023018</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024696" center_name="NIBB" accession="DRX024696">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023019</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033661" refcenter="NIBB" accession="DRS033661">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023019</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024697" center_name="NIBB" accession="DRX024697">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023019</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033661" refcenter="NIBB" accession="DRS033661">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023019</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024698" center_name="NIBB" accession="DRX024698">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023020</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033662" refcenter="NIBB" accession="DRS033662">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023020</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024699" center_name="NIBB" accession="DRX024699">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023020</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033662" refcenter="NIBB" accession="DRS033662">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023020</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024700" center_name="NIBB" accession="DRX024700">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023021</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033663" refcenter="NIBB" accession="DRS033663">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023021</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024701" center_name="NIBB" accession="DRX024701">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023021</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033663" refcenter="NIBB" accession="DRS033663">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023021</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024702" center_name="NIBB" accession="DRX024702">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023022</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033664" refcenter="NIBB" accession="DRS033664">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023022</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024703" center_name="NIBB" accession="DRX024703">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023022</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033664" refcenter="NIBB" accession="DRS033664">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023022</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024704" center_name="NIBB" accession="DRX024704">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023024</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033666" refcenter="NIBB" accession="DRS033666">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023024</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024705" center_name="NIBB" accession="DRX024705">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023024</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033666" refcenter="NIBB" accession="DRS033666">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023024</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024706" center_name="NIBB" accession="DRX024706">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023025</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033667" refcenter="NIBB" accession="DRS033667">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023025</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024707" center_name="NIBB" accession="DRX024707">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023025</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033667" refcenter="NIBB" accession="DRS033667">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023025</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024708" center_name="NIBB" accession="DRX024708">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023026</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033668" refcenter="NIBB" accession="DRS033668">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023026</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024709" center_name="NIBB" accession="DRX024709">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023026</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033668" refcenter="NIBB" accession="DRS033668">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023026</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024710" center_name="NIBB" accession="DRX024710">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023027</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033669" refcenter="NIBB" accession="DRS033669">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023027</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024711" center_name="NIBB" accession="DRX024711">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023027</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033669" refcenter="NIBB" accession="DRS033669">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023027</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024712" center_name="NIBB" accession="DRX024712">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023028</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033670" refcenter="NIBB" accession="DRS033670">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023028</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024713" center_name="NIBB" accession="DRX024713">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023028</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033670" refcenter="NIBB" accession="DRS033670">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023028</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024714" center_name="NIBB" accession="DRX024714">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023029</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033671" refcenter="NIBB" accession="DRS033671">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023029</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024715" center_name="NIBB" accession="DRX024715">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023029</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033671" refcenter="NIBB" accession="DRS033671">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023029</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024716" center_name="NIBB" accession="DRX024716">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023030</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033672" refcenter="NIBB" accession="DRS033672">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023030</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024717" center_name="NIBB" accession="DRX024717">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023030</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033672" refcenter="NIBB" accession="DRS033672">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023030</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024718" center_name="NIBB" accession="DRX024718">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023031</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033673" refcenter="NIBB" accession="DRS033673">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023031</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024719" center_name="NIBB" accession="DRX024719">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023031</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033673" refcenter="NIBB" accession="DRS033673">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023031</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024720" center_name="NIBB" accession="DRX024720">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023032</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033674" refcenter="NIBB" accession="DRS033674">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023032</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024721" center_name="NIBB" accession="DRX024721">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023032</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033674" refcenter="NIBB" accession="DRS033674">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023032</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024722" center_name="NIBB" accession="DRX024722">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023033</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033675" refcenter="NIBB" accession="DRS033675">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023033</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024723" center_name="NIBB" accession="DRX024723">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023033</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033675" refcenter="NIBB" accession="DRS033675">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023033</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024724" center_name="NIBB" accession="DRX024724">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023035</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033677" refcenter="NIBB" accession="DRS033677">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023035</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024725" center_name="NIBB" accession="DRX024725">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023035</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033677" refcenter="NIBB" accession="DRS033677">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023035</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024726" center_name="NIBB" accession="DRX024726">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023036</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033678" refcenter="NIBB" accession="DRS033678">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023036</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024727" center_name="NIBB" accession="DRX024727">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023036</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033678" refcenter="NIBB" accession="DRS033678">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023036</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024728" center_name="NIBB" accession="DRX024728">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023037</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033679" refcenter="NIBB" accession="DRS033679">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023037</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024729" center_name="NIBB" accession="DRX024729">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023037</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033679" refcenter="NIBB" accession="DRS033679">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023037</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024730" center_name="NIBB" accession="DRX024730">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023038</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033680" refcenter="NIBB" accession="DRS033680">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023038</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024731" center_name="NIBB" accession="DRX024731">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023038</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033680" refcenter="NIBB" accession="DRS033680">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023038</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024732" center_name="NIBB" accession="DRX024732">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023039</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033681" refcenter="NIBB" accession="DRS033681">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023039</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024733" center_name="NIBB" accession="DRX024733">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023039</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033681" refcenter="NIBB" accession="DRS033681">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023039</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024734" center_name="NIBB" accession="DRX024734">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023040</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033682" refcenter="NIBB" accession="DRS033682">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023040</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024735" center_name="NIBB" accession="DRX024735">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023040</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033682" refcenter="NIBB" accession="DRS033682">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023040</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024736" center_name="NIBB" accession="DRX024736">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023041</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033683" refcenter="NIBB" accession="DRS033683">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023041</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024737" center_name="NIBB" accession="DRX024737">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023041</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033683" refcenter="NIBB" accession="DRS033683">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023041</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024738" center_name="NIBB" accession="DRX024738">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023042</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033684" refcenter="NIBB" accession="DRS033684">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023042</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024739" center_name="NIBB" accession="DRX024739">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023042</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033684" refcenter="NIBB" accession="DRS033684">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023042</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024740" center_name="NIBB" accession="DRX024740">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023044</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033686" refcenter="NIBB" accession="DRS033686">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023044</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024741" center_name="NIBB" accession="DRX024741">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023044</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033686" refcenter="NIBB" accession="DRS033686">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023044</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024742" center_name="NIBB" accession="DRX024742">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023045</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033687" refcenter="NIBB" accession="DRS033687">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023045</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024743" center_name="NIBB" accession="DRX024743">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023045</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033687" refcenter="NIBB" accession="DRS033687">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023045</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024744" center_name="NIBB" accession="DRX024744">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023046</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033688" refcenter="NIBB" accession="DRS033688">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023046</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024745" center_name="NIBB" accession="DRX024745">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023046</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033688" refcenter="NIBB" accession="DRS033688">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023046</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024746" center_name="NIBB" accession="DRX024746">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023047</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033689" refcenter="NIBB" accession="DRS033689">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023047</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024747" center_name="NIBB" accession="DRX024747">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023047</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033689" refcenter="NIBB" accession="DRS033689">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023047</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024748" center_name="NIBB" accession="DRX024748">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023048</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033690" refcenter="NIBB" accession="DRS033690">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023048</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024749" center_name="NIBB" accession="DRX024749">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023048</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033690" refcenter="NIBB" accession="DRS033690">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023048</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024750" center_name="NIBB" accession="DRX024750">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023049</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033691" refcenter="NIBB" accession="DRS033691">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023049</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024751" center_name="NIBB" accession="DRX024751">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023049</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033691" refcenter="NIBB" accession="DRS033691">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023049</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024752" center_name="NIBB" accession="DRX024752">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023050</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033692" refcenter="NIBB" accession="DRS033692">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023050</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024753" center_name="NIBB" accession="DRX024753">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023050</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033692" refcenter="NIBB" accession="DRS033692">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023050</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024754" center_name="NIBB" accession="DRX024754">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023051</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033693" refcenter="NIBB" accession="DRS033693">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023051</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024755" center_name="NIBB" accession="DRX024755">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023051</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033693" refcenter="NIBB" accession="DRS033693">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023051</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024756" center_name="NIBB" accession="DRX024756">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023052</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033694" refcenter="NIBB" accession="DRS033694">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023052</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024757" center_name="NIBB" accession="DRX024757">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023052</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033694" refcenter="NIBB" accession="DRS033694">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023052</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024758" center_name="NIBB" accession="DRX024758">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023053</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033695" refcenter="NIBB" accession="DRS033695">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023053</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024759" center_name="NIBB" accession="DRX024759">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023053</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033695" refcenter="NIBB" accession="DRS033695">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023053</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024760" center_name="NIBB" accession="DRX024760">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023055</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033697" refcenter="NIBB" accession="DRS033697">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023055</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024761" center_name="NIBB" accession="DRX024761">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023055</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033697" refcenter="NIBB" accession="DRS033697">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023055</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024762" center_name="NIBB" accession="DRX024762">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023056</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033698" refcenter="NIBB" accession="DRS033698">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023056</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024763" center_name="NIBB" accession="DRX024763">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023056</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033698" refcenter="NIBB" accession="DRS033698">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023056</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024764" center_name="NIBB" accession="DRX024764">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023057</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033699" refcenter="NIBB" accession="DRS033699">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023057</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024765" center_name="NIBB" accession="DRX024765">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023057</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033699" refcenter="NIBB" accession="DRS033699">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023057</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024766" center_name="NIBB" accession="DRX024766">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023058</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033700" refcenter="NIBB" accession="DRS033700">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023058</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024767" center_name="NIBB" accession="DRX024767">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023058</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033700" refcenter="NIBB" accession="DRS033700">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023058</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024768" center_name="NIBB" accession="DRX024768">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023059</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033701" refcenter="NIBB" accession="DRS033701">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023059</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024769" center_name="NIBB" accession="DRX024769">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023059</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033701" refcenter="NIBB" accession="DRS033701">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023059</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024770" center_name="NIBB" accession="DRX024770">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023060</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033702" refcenter="NIBB" accession="DRS033702">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023060</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024771" center_name="NIBB" accession="DRX024771">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023060</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033702" refcenter="NIBB" accession="DRS033702">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023060</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024772" center_name="NIBB" accession="DRX024772">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023061</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033703" refcenter="NIBB" accession="DRS033703">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023061</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024773" center_name="NIBB" accession="DRX024773">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023061</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033703" refcenter="NIBB" accession="DRS033703">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023061</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024774" center_name="NIBB" accession="DRX024774">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023062</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033704" refcenter="NIBB" accession="DRS033704">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023062</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024775" center_name="NIBB" accession="DRX024775">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023062</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033704" refcenter="NIBB" accession="DRS033704">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023062</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024776" center_name="NIBB" accession="DRX024776">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023063</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033705" refcenter="NIBB" accession="DRS033705">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023063</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024777" center_name="NIBB" accession="DRX024777">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023063</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033705" refcenter="NIBB" accession="DRS033705">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023063</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024778" center_name="NIBB" accession="DRX024778">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023064</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033706" refcenter="NIBB" accession="DRS033706">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023064</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024779" center_name="NIBB" accession="DRX024779">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023064</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033706" refcenter="NIBB" accession="DRS033706">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023064</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024780" center_name="NIBB" accession="DRX024780">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023066</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033708" refcenter="NIBB" accession="DRS033708">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023066</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024781" center_name="NIBB" accession="DRX024781">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023066</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033708" refcenter="NIBB" accession="DRS033708">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023066</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024782" center_name="NIBB" accession="DRX024782">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023067</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033709" refcenter="NIBB" accession="DRS033709">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023067</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024783" center_name="NIBB" accession="DRX024783">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023067</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033709" refcenter="NIBB" accession="DRS033709">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023067</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024784" center_name="NIBB" accession="DRX024784">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023068</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033710" refcenter="NIBB" accession="DRS033710">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023068</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024785" center_name="NIBB" accession="DRX024785">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023068</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033710" refcenter="NIBB" accession="DRS033710">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023068</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024786" center_name="NIBB" accession="DRX024786">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023069</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033711" refcenter="NIBB" accession="DRS033711">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023069</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024787" center_name="NIBB" accession="DRX024787">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023069</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033711" refcenter="NIBB" accession="DRS033711">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023069</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024788" center_name="NIBB" accession="DRX024788">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023070</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033712" refcenter="NIBB" accession="DRS033712">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023070</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024789" center_name="NIBB" accession="DRX024789">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023070</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033712" refcenter="NIBB" accession="DRS033712">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023070</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024790" center_name="NIBB" accession="DRX024790">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023071</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033713" refcenter="NIBB" accession="DRS033713">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023071</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024791" center_name="NIBB" accession="DRX024791">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023071</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033713" refcenter="NIBB" accession="DRS033713">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023071</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024792" center_name="NIBB" accession="DRX024792">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023072</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033714" refcenter="NIBB" accession="DRS033714">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023072</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024793" center_name="NIBB" accession="DRX024793">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023072</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033714" refcenter="NIBB" accession="DRS033714">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023072</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024794" center_name="NIBB" accession="DRX024794">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023073</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033715" refcenter="NIBB" accession="DRS033715">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023073</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024795" center_name="NIBB" accession="DRX024795">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023073</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033715" refcenter="NIBB" accession="DRS033715">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023073</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024796" center_name="NIBB" accession="DRX024796">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023074</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033716" refcenter="NIBB" accession="DRS033716">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023074</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024797" center_name="NIBB" accession="DRX024797">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023074</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033716" refcenter="NIBB" accession="DRS033716">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023074</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024798" center_name="NIBB" accession="DRX024798">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023075</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033717" refcenter="NIBB" accession="DRS033717">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023075</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024799" center_name="NIBB" accession="DRX024799">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023075</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033717" refcenter="NIBB" accession="DRS033717">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023075</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024800" center_name="NIBB" accession="DRX024800">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023077</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033719" refcenter="NIBB" accession="DRS033719">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023077</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024801" center_name="NIBB" accession="DRX024801">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023077</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033719" refcenter="NIBB" accession="DRS033719">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023077</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024802" center_name="NIBB" accession="DRX024802">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023078</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033720" refcenter="NIBB" accession="DRS033720">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023078</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024803" center_name="NIBB" accession="DRX024803">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023078</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033720" refcenter="NIBB" accession="DRS033720">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023078</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024804" center_name="NIBB" accession="DRX024804">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023079</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033721" refcenter="NIBB" accession="DRS033721">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023079</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024805" center_name="NIBB" accession="DRX024805">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023079</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033721" refcenter="NIBB" accession="DRS033721">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023079</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024806" center_name="NIBB" accession="DRX024806">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023080</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033722" refcenter="NIBB" accession="DRS033722">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023080</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024807" center_name="NIBB" accession="DRX024807">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023080</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033722" refcenter="NIBB" accession="DRS033722">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023080</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024808" center_name="NIBB" accession="DRX024808">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023081</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033723" refcenter="NIBB" accession="DRS033723">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023081</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024809" center_name="NIBB" accession="DRX024809">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023081</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033723" refcenter="NIBB" accession="DRS033723">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023081</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024810" center_name="NIBB" accession="DRX024810">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023082</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033724" refcenter="NIBB" accession="DRS033724">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023082</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024811" center_name="NIBB" accession="DRX024811">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023082</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033724" refcenter="NIBB" accession="DRS033724">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023082</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024812" center_name="NIBB" accession="DRX024812">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023083</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033725" refcenter="NIBB" accession="DRS033725">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023083</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024813" center_name="NIBB" accession="DRX024813">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023083</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033725" refcenter="NIBB" accession="DRS033725">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023083</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_4</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024814" center_name="NIBB" accession="DRX024814">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023084</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033726" refcenter="NIBB" accession="DRS033726">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023084</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024815" center_name="NIBB" accession="DRX024815">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023084</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033726" refcenter="NIBB" accession="DRS033726">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023084</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024816" center_name="NIBB" accession="DRX024816">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023085</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033727" refcenter="NIBB" accession="DRS033727">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023085</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024817" center_name="NIBB" accession="DRX024817">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023085</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033727" refcenter="NIBB" accession="DRS033727">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023085</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024818" center_name="NIBB" accession="DRX024818">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023086</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033728" refcenter="NIBB" accession="DRS033728">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023086</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024819" center_name="NIBB" accession="DRX024819">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023086</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033728" refcenter="NIBB" accession="DRS033728">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023086</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024820" center_name="NIBB" accession="DRX024820">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023089</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033731" refcenter="NIBB" accession="DRS033731">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023089</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024821" center_name="NIBB" accession="DRX024821">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023089</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033731" refcenter="NIBB" accession="DRS033731">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023089</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024822" center_name="NIBB" accession="DRX024822">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023090</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033732" refcenter="NIBB" accession="DRS033732">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023090</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024823" center_name="NIBB" accession="DRX024823">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023090</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033732" refcenter="NIBB" accession="DRS033732">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023090</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024824" center_name="NIBB" accession="DRX024824">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023091</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033733" refcenter="NIBB" accession="DRS033733">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023091</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024825" center_name="NIBB" accession="DRX024825">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023091</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033733" refcenter="NIBB" accession="DRS033733">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023091</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024826" center_name="NIBB" accession="DRX024826">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023092</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033734" refcenter="NIBB" accession="DRS033734">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023092</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024827" center_name="NIBB" accession="DRX024827">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023092</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033734" refcenter="NIBB" accession="DRS033734">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023092</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024828" center_name="NIBB" accession="DRX024828">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023093</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033735" refcenter="NIBB" accession="DRS033735">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023093</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024829" center_name="NIBB" accession="DRX024829">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023093</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033735" refcenter="NIBB" accession="DRS033735">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023093</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024830" center_name="NIBB" accession="DRX024830">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023094</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033736" refcenter="NIBB" accession="DRS033736">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023094</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024831" center_name="NIBB" accession="DRX024831">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023094</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033736" refcenter="NIBB" accession="DRS033736">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023094</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024832" center_name="NIBB" accession="DRX024832">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023095</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033737" refcenter="NIBB" accession="DRS033737">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023095</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024833" center_name="NIBB" accession="DRX024833">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023095</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033737" refcenter="NIBB" accession="DRS033737">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023095</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024834" center_name="NIBB" accession="DRX024834">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023096</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033738" refcenter="NIBB" accession="DRS033738">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023096</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024835" center_name="NIBB" accession="DRX024835">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023096</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033738" refcenter="NIBB" accession="DRS033738">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023096</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024836" center_name="NIBB" accession="DRX024836">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023097</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033739" refcenter="NIBB" accession="DRS033739">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023097</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024837" center_name="NIBB" accession="DRX024837">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023097</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033739" refcenter="NIBB" accession="DRS033739">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023097</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024838" center_name="NIBB" accession="DRX024838">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023099</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033741" refcenter="NIBB" accession="DRS033741">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023099</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024839" center_name="NIBB" accession="DRX024839">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023099</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033741" refcenter="NIBB" accession="DRS033741">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023099</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024840" center_name="NIBB" accession="DRX024840">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022977</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033619" refcenter="NIBB" accession="DRS033619">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022977</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024841" center_name="NIBB" accession="DRX024841">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022977</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033619" refcenter="NIBB" accession="DRS033619">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022977</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024842" center_name="NIBB" accession="DRX024842">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022977</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033619" refcenter="NIBB" accession="DRS033619">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022977</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024843" center_name="NIBB" accession="DRX024843">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00022977</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033619" refcenter="NIBB" accession="DRS033619">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00022977</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024844" center_name="NIBB" accession="DRX024844">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023185</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033827" refcenter="NIBB" accession="DRS033827">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023185</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024845" center_name="NIBB" accession="DRX024845">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023185</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033827" refcenter="NIBB" accession="DRS033827">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023185</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD1_3</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024846" center_name="NIBB" accession="DRX024846">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023185</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033827" refcenter="NIBB" accession="DRS033827">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023185</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_1</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with MseI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
    <EXPERIMENT alias="DRX024847" center_name="NIBB" accession="DRX024847">
        <TITLE>Illumina HiSeq 2500 sequencing of SAMD00023185</TITLE>
        <STUDY_REF refname="DRP003256" refcenter="NIBB" accession="DRP003256">
            <IDENTIFIERS>
                <PRIMARY_ID label="BioProject ID">PRJDB4356</PRIMARY_ID>
            </IDENTIFIERS>
        </STUDY_REF>
        <DESIGN>
            <DESIGN_DESCRIPTION></DESIGN_DESCRIPTION>
            <SAMPLE_DESCRIPTOR refname="DRS033827" refcenter="NIBB" accession="DRS033827">
                <IDENTIFIERS>
                    <PRIMARY_ID label="BioSample ID">SAMD00023185</PRIMARY_ID>
                </IDENTIFIERS>
            </SAMPLE_DESCRIPTOR>
            <LIBRARY_DESCRIPTOR>
                <LIBRARY_NAME>IpeRAD2_2</LIBRARY_NAME>
                <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
                <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
                <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
                <LIBRARY_LAYOUT>
                    <SINGLE/>
                </LIBRARY_LAYOUT>
                <LIBRARY_CONSTRUCTION_PROTOCOL>Genomic DNA was digested with NdeI and BglII and ligated with adaptors. The ligation products were purified using AMPure XP kit (Beckman Coulter) and were amplified by PCR. The PCR products from multiple samples were pooled, and the pooled DNA fragments were concentrated using AMPure XP kit. For size selection, E-gel SizeSelect (LifeTechnologies) was used, and approximately 350 bp fragments were retrieved and purified.</LIBRARY_CONSTRUCTION_PROTOCOL>
            </LIBRARY_DESCRIPTOR>
            <SPOT_DESCRIPTOR>
                <SPOT_DECODE_SPEC>
                    <SPOT_LENGTH>150</SPOT_LENGTH>
                    <READ_SPEC>
                        <READ_INDEX>0</READ_INDEX>
                        <READ_CLASS>Application Read</READ_CLASS>
                        <READ_TYPE>Forward</READ_TYPE>
                        <BASE_COORD>1</BASE_COORD>
                    </READ_SPEC>
                </SPOT_DECODE_SPEC>
            </SPOT_DESCRIPTOR>
        </DESIGN>
        <PLATFORM>
            <ILLUMINA>
                <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
            </ILLUMINA>
        </PLATFORM>
    </EXPERIMENT>
</EXPERIMENT_SET>
