<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT alias="A1_2" accession="SRX1043799">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1043799</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Georgia">A1_2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Ab10I-MMR mRNA, sample 1</TITLE>
    <STUDY_REF accession="SRP058857">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP058857</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Frozen anthers were hand ground with a plastic pestle in Buffer RF, the stabilizing extraction buffer from Qiagen RNeasy Plant Mini kit (Cat# 74903). The protocol from the kit was then followed as specified to isolate RNA. mRNA sequencing libraries were prepared using a stranded Kapa Biosystems mRNA kit, Cat# KK8420 with dual indexing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS949259">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS949259</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Ab10I-MMR mRNA, sample 1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_SDEV="0.0E0"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>152</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>77</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="A1_3" accession="SRX1043800">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1043800</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Georgia">A1_3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Ab10I-MMR mRNA, sample 2</TITLE>
    <STUDY_REF accession="SRP058857">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP058857</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Frozen anthers were hand ground with a plastic pestle in Buffer RF, the stabilizing extraction buffer from Qiagen RNeasy Plant Mini kit (Cat# 74903). The protocol from the kit was then followed as specified to isolate RNA. mRNA sequencing libraries were prepared using a stranded Kapa Biosystems mRNA kit, Cat# KK8420 with dual indexing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS949260">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS949260</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Ab10I-MMR mRNA, sample 2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_SDEV="0.0E0"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>152</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>77</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="A1_6" accession="SRX1043801">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1043801</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Georgia">A1_6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Ab10I-MMR mRNA, sample 3</TITLE>
    <STUDY_REF accession="SRP058857">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP058857</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Frozen anthers were hand ground with a plastic pestle in Buffer RF, the stabilizing extraction buffer from Qiagen RNeasy Plant Mini kit (Cat# 74903). The protocol from the kit was then followed as specified to isolate RNA. mRNA sequencing libraries were prepared using a stranded Kapa Biosystems mRNA kit, Cat# KK8420 with dual indexing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS949261">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS949261</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Ab10I-MMR mRNA, sample 3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_SDEV="0.0E0"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>152</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>77</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="A2_1" accession="SRX1043802">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1043802</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Georgia">A2_1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Ab10II-MMR mRNA, sample 1</TITLE>
    <STUDY_REF accession="SRP058857">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP058857</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Frozen anthers were hand ground with a plastic pestle in Buffer RF, the stabilizing extraction buffer from Qiagen RNeasy Plant Mini kit (Cat# 74903). The protocol from the kit was then followed as specified to isolate RNA. mRNA sequencing libraries were prepared using a stranded Kapa Biosystems mRNA kit, Cat# KK8420 with dual indexing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS949262">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS949262</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Ab10II-MMR mRNA, sample 1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_SDEV="0.0E0"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>152</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>77</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="A2_3" accession="SRX1043804">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1043804</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Georgia">A2_3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Ab10II-MMR mRNA, sample 2</TITLE>
    <STUDY_REF accession="SRP058857">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP058857</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>mRNA-seq of maize abnormal chromosome 10 variants  PRJNA285341  SAMN03744095  Frozen anthers were hand ground with a plastic pestle in Buffer RF, the stabilizing extraction buffer from Qiagen RNeasy Plant Mini kit (Cat# 74903). The protocol from the kit was then followed as specified to isolate RNA. mRNA sequencing libraries were prepared using a stranded Kapa Biosystems mRNA kit, Cat# KK8420 with dual indexing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS949264">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS949264</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Ab10II-MMR mRNA, sample 2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_SDEV="0.0E0"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>152</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>77</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="A2_4" accession="SRX1043806">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1043806</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Georgia">A2_4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Ab10II-MMR mRNA, sample 3</TITLE>
    <STUDY_REF accession="SRP058857">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP058857</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Frozen anthers were hand ground with a plastic pestle in Buffer RF, the stabilizing extraction buffer from Qiagen RNeasy Plant Mini kit (Cat# 74903). The protocol from the kit was then followed as specified to isolate RNA. mRNA sequencing libraries were prepared using a stranded Kapa Biosystems mRNA kit, Cat# KK8420 with dual indexing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS949266">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS949266</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Ab10II-MMR mRNA, sample 3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_SDEV="0.0E0"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>152</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>77</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="AL2_1" accession="SRX1043810">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1043810</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Georgia">AL2_1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>K10L2 mRNA, sample 1</TITLE>
    <STUDY_REF accession="SRP058857">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP058857</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Frozen anthers were hand ground with a plastic pestle in Buffer RF, the stabilizing extraction buffer from Qiagen RNeasy Plant Mini kit (Cat# 74903). The protocol from the kit was then followed as specified to isolate RNA. mRNA sequencing libraries were prepared using a stranded Kapa Biosystems mRNA kit, Cat# KK8420 with dual indexing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS949269">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS949269</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>K10L2 mRNA, sample 1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_SDEV="0.0E0"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>152</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>77</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="AL2_3" accession="SRX1043812">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1043812</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Georgia">AL2_3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>K10L2 mRNA, sample 2</TITLE>
    <STUDY_REF accession="SRP058857">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP058857</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Frozen anthers were hand ground with a plastic pestle in Buffer RF, the stabilizing extraction buffer from Qiagen RNeasy Plant Mini kit (Cat# 74903). The protocol from the kit was then followed as specified to isolate RNA. mRNA sequencing libraries were prepared using a stranded Kapa Biosystems mRNA kit, Cat# KK8420 with dual indexing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS949273">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS949273</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>K10L2 mRNA, sample 2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_SDEV="0.0E0"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>152</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>77</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="AL2_4" accession="SRX1043815">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1043815</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Georgia">AL2_4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>K10L2 mRNA, sample 3</TITLE>
    <STUDY_REF accession="SRP058857">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP058857</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Frozen anthers were hand ground with a plastic pestle in Buffer RF, the stabilizing extraction buffer from Qiagen RNeasy Plant Mini kit (Cat# 74903). The protocol from the kit was then followed as specified to isolate RNA. mRNA sequencing libraries were prepared using a stranded Kapa Biosystems mRNA kit, Cat# KK8420 with dual indexing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS949274">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS949274</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>K10L2 mRNA, sample 3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_SDEV="0.0E0"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>152</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>77</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="AL2_5" accession="SRX1043818">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1043818</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Georgia">AL2_5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>K10L2 mRNA, sample 4</TITLE>
    <STUDY_REF accession="SRP058857">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP058857</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Frozen anthers were hand ground with a plastic pestle in Buffer RF, the stabilizing extraction buffer from Qiagen RNeasy Plant Mini kit (Cat# 74903). The protocol from the kit was then followed as specified to isolate RNA. mRNA sequencing libraries were prepared using a stranded Kapa Biosystems mRNA kit, Cat# KK8420 with dual indexing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS949277">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS949277</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>K10L2 mRNA, sample 4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_SDEV="0.0E0"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>152</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>77</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="AL2_6" accession="SRX1043820">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1043820</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Georgia">AL2_6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>K10L2 mRNA, sample 5</TITLE>
    <STUDY_REF accession="SRP058857">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP058857</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Frozen anthers were hand ground with a plastic pestle in Buffer RF, the stabilizing extraction buffer from Qiagen RNeasy Plant Mini kit (Cat# 74903). The protocol from the kit was then followed as specified to isolate RNA. mRNA sequencing libraries were prepared using a stranded Kapa Biosystems mRNA kit, Cat# KK8420 with dual indexing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS949281">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS949281</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>K10L2 mRNA, sample 5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_SDEV="0.0E0"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>152</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>77</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="K2_2" accession="SRX1043822">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1043822</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Georgia">K2_2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Ab10-II-Tel mRNA, sample 1</TITLE>
    <STUDY_REF accession="SRP058857">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP058857</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Frozen anthers were hand ground with a plastic pestle in Buffer RF, the stabilizing extraction buffer from Qiagen RNeasy Plant Mini kit (Cat# 74903). The protocol from the kit was then followed as specified to isolate RNA. mRNA sequencing libraries were prepared using a stranded Kapa Biosystems mRNA kit, Cat# KK8420 with dual indexing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS949282">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS949282</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Ab10-II-Tel mRNA, sample 1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_SDEV="0.0E0"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>152</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>77</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="K2_3" accession="SRX1043823">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1043823</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Georgia">K2_3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Ab10-II-Tel mRNA, sample 2</TITLE>
    <STUDY_REF accession="SRP058857">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP058857</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Frozen anthers were hand ground with a plastic pestle in Buffer RF, the stabilizing extraction buffer from Qiagen RNeasy Plant Mini kit (Cat# 74903). The protocol from the kit was then followed as specified to isolate RNA. mRNA sequencing libraries were prepared using a stranded Kapa Biosystems mRNA kit, Cat# KK8420 with dual indexing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS949283">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS949283</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Ab10-II-Tel mRNA, sample 2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_SDEV="0.0E0"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>152</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>77</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="K2_6" accession="SRX1043824">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1043824</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Georgia">K2_6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Ab10-II-Tel mRNA, sample 3</TITLE>
    <STUDY_REF accession="SRP058857">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP058857</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Frozen anthers were hand ground with a plastic pestle in Buffer RF, the stabilizing extraction buffer from Qiagen RNeasy Plant Mini kit (Cat# 74903). The protocol from the kit was then followed as specified to isolate RNA. mRNA sequencing libraries were prepared using a stranded Kapa Biosystems mRNA kit, Cat# KK8420 with dual indexing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS949284">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS949284</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Ab10-II-Tel mRNA, sample 3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_SDEV="0.0E0"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>152</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>77</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="N1_1" accession="SRX1043881">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1043881</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Georgia">N1_1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>N10 control (for Ab10I-MMR) mRNA, sample 1</TITLE>
    <STUDY_REF accession="SRP058857">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP058857</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Frozen anthers were hand ground with a plastic pestle in Buffer RF, the stabilizing extraction buffer from Qiagen RNeasy Plant Mini kit (Cat# 74903). The protocol from the kit was then followed as specified to isolate RNA. mRNA sequencing libraries were prepared using a stranded Kapa Biosystems mRNA kit, Cat# KK8420 with dual indexing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS949326">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS949326</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>N10 control (for Ab10I-MMR) mRNA, sample 1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_SDEV="0.0E0"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>152</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>77</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="N1_3" accession="SRX1043882">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1043882</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Georgia">N1_3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>N10 control (for Ab10I-MMR) mRNA, sample 2</TITLE>
    <STUDY_REF accession="SRP058857">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP058857</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Frozen anthers were hand ground with a plastic pestle in Buffer RF, the stabilizing extraction buffer from Qiagen RNeasy Plant Mini kit (Cat# 74903). The protocol from the kit was then followed as specified to isolate RNA. mRNA sequencing libraries were prepared using a stranded Kapa Biosystems mRNA kit, Cat# KK8420 with dual indexing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS949329">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS949329</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>N10 control (for Ab10I-MMR) mRNA, sample 2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_SDEV="0.0E0"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>152</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>77</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="N1_6" accession="SRX1043883">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1043883</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Georgia">N1_6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>N10 control (for Ab10I-MMR) mRNA, sample 3</TITLE>
    <STUDY_REF accession="SRP058857">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP058857</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Frozen anthers were hand ground with a plastic pestle in Buffer RF, the stabilizing extraction buffer from Qiagen RNeasy Plant Mini kit (Cat# 74903). The protocol from the kit was then followed as specified to isolate RNA. mRNA sequencing libraries were prepared using a stranded Kapa Biosystems mRNA kit, Cat# KK8420 with dual indexing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS949328">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS949328</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>N10 control (for Ab10I-MMR) mRNA, sample 3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_SDEV="0.0E0"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>152</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>77</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="N2_1" accession="SRX1043884">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1043884</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Georgia">N2_1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>N10 control (for Ab10II-MMR) mRNA, sample 1</TITLE>
    <STUDY_REF accession="SRP058857">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP058857</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Frozen anthers were hand ground with a plastic pestle in Buffer RF, the stabilizing extraction buffer from Qiagen RNeasy Plant Mini kit (Cat# 74903). The protocol from the kit was then followed as specified to isolate RNA. mRNA sequencing libraries were prepared using a stranded Kapa Biosystems mRNA kit, Cat# KK8420 with dual indexing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS949327">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS949327</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>N10 control (for Ab10II-MMR) mRNA, sample 1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_SDEV="0.0E0"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>152</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>77</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="N2_5" accession="SRX1043886">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1043886</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Georgia">N2_5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>N10 control (for Ab10II-MMR) mRNA, sample 2</TITLE>
    <STUDY_REF accession="SRP058857">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP058857</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Frozen anthers were hand ground with a plastic pestle in Buffer RF, the stabilizing extraction buffer from Qiagen RNeasy Plant Mini kit (Cat# 74903). The protocol from the kit was then followed as specified to isolate RNA. mRNA sequencing libraries were prepared using a stranded Kapa Biosystems mRNA kit, Cat# KK8420 with dual indexing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS949331">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS949331</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>N10 control (for Ab10II-MMR) mRNA, sample 2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_SDEV="0.0E0"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>152</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>77</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="N2_6" accession="SRX1043887">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1043887</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Georgia">N2_6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>N10 control (for Ab10II-MMR) mRNA, sample 3</TITLE>
    <STUDY_REF accession="SRP058857">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP058857</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Frozen anthers were hand ground with a plastic pestle in Buffer RF, the stabilizing extraction buffer from Qiagen RNeasy Plant Mini kit (Cat# 74903). The protocol from the kit was then followed as specified to isolate RNA. mRNA sequencing libraries were prepared using a stranded Kapa Biosystems mRNA kit, Cat# KK8420 with dual indexing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS949332">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS949332</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>N10 control (for Ab10II-MMR) mRNA, sample 3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_SDEV="0.0E0"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>152</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>77</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="NK2_4" accession="SRX1043888">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1043888</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Georgia">NK2_4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>N10 control (for Ab10II-Tel) mRNA, sample 1</TITLE>
    <STUDY_REF accession="SRP058857">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP058857</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Frozen anthers were hand ground with a plastic pestle in Buffer RF, the stabilizing extraction buffer from Qiagen RNeasy Plant Mini kit (Cat# 74903). The protocol from the kit was then followed as specified to isolate RNA. mRNA sequencing libraries were prepared using a stranded Kapa Biosystems mRNA kit, Cat# KK8420 with dual indexing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS949333">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS949333</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>N10 control (for Ab10II-Tel) mRNA, sample 1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_SDEV="0.0E0"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>152</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>77</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="NK2_8" accession="SRX1043890">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1043890</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Georgia">NK2_8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>N10 control (for Ab10II-Tel) mRNA, sample 2</TITLE>
    <STUDY_REF accession="SRP058857">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP058857</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Frozen anthers were hand ground with a plastic pestle in Buffer RF, the stabilizing extraction buffer from Qiagen RNeasy Plant Mini kit (Cat# 74903). The protocol from the kit was then followed as specified to isolate RNA. mRNA sequencing libraries were prepared using a stranded Kapa Biosystems mRNA kit, Cat# KK8420 with dual indexing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS949334">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS949334</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>N10 control (for Ab10II-Tel) mRNA, sample 2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_SDEV="0.0E0"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>152</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>77</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="NK2_9" accession="SRX1043892">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1043892</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Georgia">NK2_9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>N10 control (for Ab10II-Tel) mRNA, sample 3</TITLE>
    <STUDY_REF accession="SRP058857">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP058857</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Frozen anthers were hand ground with a plastic pestle in Buffer RF, the stabilizing extraction buffer from Qiagen RNeasy Plant Mini kit (Cat# 74903). The protocol from the kit was then followed as specified to isolate RNA. mRNA sequencing libraries were prepared using a stranded Kapa Biosystems mRNA kit, Cat# KK8420 with dual indexing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS949335">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS949335</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>N10 control (for Ab10II-Tel) mRNA, sample 3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_SDEV="0.0E0"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>152</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>77</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="NL2_2" accession="SRX1043894">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1043894</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Georgia">NL2_2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>N10 control (for K10L2) mRNA, sample 1</TITLE>
    <STUDY_REF accession="SRP058857">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP058857</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Frozen anthers were hand ground with a plastic pestle in Buffer RF, the stabilizing extraction buffer from Qiagen RNeasy Plant Mini kit (Cat# 74903). The protocol from the kit was then followed as specified to isolate RNA. mRNA sequencing libraries were prepared using a stranded Kapa Biosystems mRNA kit, Cat# KK8420 with dual indexing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS949336">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS949336</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>N10 control (for K10L2) mRNA, sample 1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_SDEV="0.0E0"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>152</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>77</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="NL2_5" accession="SRX1043895">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1043895</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Georgia">NL2_5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>N10 control (for K10L2) mRNA, sample 3</TITLE>
    <STUDY_REF accession="SRP058857">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP058857</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Frozen anthers were hand ground with a plastic pestle in Buffer RF, the stabilizing extraction buffer from Qiagen RNeasy Plant Mini kit (Cat# 74903). The protocol from the kit was then followed as specified to isolate RNA. mRNA sequencing libraries were prepared using a stranded Kapa Biosystems mRNA kit, Cat# KK8420 with dual indexing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS949338">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS949338</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>N10 control (for K10L2) mRNA, sample 3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_SDEV="0.0E0"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>152</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>77</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="NL2_3" accession="SRX1043897">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1043897</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Georgia">NL2_3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>N10 control (for K10L2) mRNA, sample 2</TITLE>
    <STUDY_REF accession="SRP058857">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP058857</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Frozen anthers were hand ground with a plastic pestle in Buffer RF, the stabilizing extraction buffer from Qiagen RNeasy Plant Mini kit (Cat# 74903). The protocol from the kit was then followed as specified to isolate RNA. mRNA sequencing libraries were prepared using a stranded Kapa Biosystems mRNA kit, Cat# KK8420 with dual indexing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS949339">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS949339</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>N10 control (for K10L2) mRNA, sample 2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_SDEV="0.0E0"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>152</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>77</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="X_A1" accession="SRX1043966">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1043966</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Georgia">X_A1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Ab10I-Pue mRNA, sample 1</TITLE>
    <STUDY_REF accession="SRP058857">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP058857</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Frozen anthers were hand ground with a plastic pestle in Buffer RF, the stabilizing extraction buffer from Qiagen RNeasy Plant Mini kit (Cat# 74903). The protocol from the kit was then followed as specified to isolate RNA. mRNA sequencing libraries were prepared using a stranded Kapa Biosystems mRNA kit, Cat# KK8420 with dual indexing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS949404">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS949404</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Ab10I-Pue mRNA, sample 1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_SDEV="0.0E0"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>152</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>77</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="X_A2" accession="SRX1043967">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1043967</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Georgia">X_A2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Ab10I-Pue mRNA, sample 2</TITLE>
    <STUDY_REF accession="SRP058857">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP058857</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Frozen anthers were hand ground with a plastic pestle in Buffer RF, the stabilizing extraction buffer from Qiagen RNeasy Plant Mini kit (Cat# 74903). The protocol from the kit was then followed as specified to isolate RNA. mRNA sequencing libraries were prepared using a stranded Kapa Biosystems mRNA kit, Cat# KK8420 with dual indexing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS949405">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS949405</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Ab10I-Pue mRNA, sample 2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_SDEV="0.0E0"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>152</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>77</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="X_A4" accession="SRX1043968">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1043968</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Georgia">X_A4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Ab10I-Pue mRNA, sample 3</TITLE>
    <STUDY_REF accession="SRP058857">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP058857</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Frozen anthers were hand ground with a plastic pestle in Buffer RF, the stabilizing extraction buffer from Qiagen RNeasy Plant Mini kit (Cat# 74903). The protocol from the kit was then followed as specified to isolate RNA. mRNA sequencing libraries were prepared using a stranded Kapa Biosystems mRNA kit, Cat# KK8420 with dual indexing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS949406">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS949406</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Ab10I-Pue mRNA, sample 3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_SDEV="0.0E0"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>152</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>77</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="X_N1" accession="SRX1043979">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1043979</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Georgia">X_N1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>N10 control (for Ab101-Pue) mRNA, sample 1</TITLE>
    <STUDY_REF accession="SRP058857">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP058857</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Frozen anthers were hand ground with a plastic pestle in Buffer RF, the stabilizing extraction buffer from Qiagen RNeasy Plant Mini kit (Cat# 74903). The protocol from the kit was then followed as specified to isolate RNA. mRNA sequencing libraries were prepared using a stranded Kapa Biosystems mRNA kit, Cat# KK8420 with dual indexing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS949419">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS949419</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>N10 control (for Ab101-Pue) mRNA, sample 1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_SDEV="0.0E0"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>152</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>77</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="X_N2" accession="SRX1043991">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1043991</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Georgia">X_N2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>N10 control (for Ab101-Pue) mRNA, sample 2</TITLE>
    <STUDY_REF accession="SRP058857">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP058857</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Frozen anthers were hand ground with a plastic pestle in Buffer RF, the stabilizing extraction buffer from Qiagen RNeasy Plant Mini kit (Cat# 74903). The protocol from the kit was then followed as specified to isolate RNA. mRNA sequencing libraries were prepared using a stranded Kapa Biosystems mRNA kit, Cat# KK8420 with dual indexing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS949429">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS949429</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>N10 control (for Ab101-Pue) mRNA, sample 2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_SDEV="0.0E0"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>152</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>77</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="PRJNA285341" accession="SRX1044004">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1044004</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Georgia">PRJNA285341</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>N10 control (for Ab101-Pue) mRNA, sample 3</TITLE>
    <STUDY_REF accession="SRP058857">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP058857</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Frozen anthers were hand ground with a plastic pestle in Buffer RF, the stabilizing extraction buffer from Qiagen RNeasy Plant Mini kit (Cat# 74903). The protocol from the kit was then followed as specified to isolate RNA. mRNA sequencing libraries were prepared using a stranded Kapa Biosystems mRNA kit, Cat# KK8420 with dual indexing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS949430">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS949430</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>X_N3N10 control (for Ab101-Pue) mRNA, sample 3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_SDEV="0.0E0"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>152</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>77</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
