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      <PRIMARY_ID>SRX647212</PRIMARY_ID>
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    <TITLE>GSM1428527: Change 7-2; Zea mays; ncRNA-Seq</TITLE>
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        <PRIMARY_ID>SRP044085</PRIMARY_ID>
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          <SINGLE/>
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        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA from the all samples was extracted with TRIzol reagent (Invitrogen, 15596-026) following the manufacturer’s protocol. Small RNA libraies were constructed by TruSeq Small RNA Sample Prep Kit (Illumina) following the manufacturer’s instructions. Briefly, 1 µg total RNA or purified small RNA was ligated with 3’ and 5’ adaptors and used as a template for RT-PCR. After PCR amplification, 6 µL of each sample were pooled and separated on a 6% polyacrylamide Gel. Gel slices corresponding to ~18-26 nt small RNAs were recovered.</LIBRARY_CONSTRUCTION_PROTOCOL>
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        <INSTRUMENT_MODEL>Illumina Genome Analyzer II</INSTRUMENT_MODEL>
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      <EXPERIMENT_LINK>
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          <LABEL>GEO Sample GSM1428527</LABEL>
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      <PRIMARY_ID>SRX647213</PRIMARY_ID>
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    <TITLE>GSM1428528: Zheng 58; Zea mays; ncRNA-Seq</TITLE>
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        <PRIMARY_ID>SRP044085</PRIMARY_ID>
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        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA from the all samples was extracted with TRIzol reagent (Invitrogen, 15596-026) following the manufacturer’s protocol. Small RNA libraies were constructed by TruSeq Small RNA Sample Prep Kit (Illumina) following the manufacturer’s instructions. Briefly, 1 µg total RNA or purified small RNA was ligated with 3’ and 5’ adaptors and used as a template for RT-PCR. After PCR amplification, 6 µL of each sample were pooled and separated on a 6% polyacrylamide Gel. Gel slices corresponding to ~18-26 nt small RNAs were recovered.</LIBRARY_CONSTRUCTION_PROTOCOL>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina Genome Analyzer II</INSTRUMENT_MODEL>
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      <EXPERIMENT_LINK>
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      <PRIMARY_ID>SRX647214</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1428529</SUBMITTER_ID>
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    <TITLE>GSM1428529: Zhengdan 958; Zea mays; ncRNA-Seq</TITLE>
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        <PRIMARY_ID>SRP044085</PRIMARY_ID>
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          <PRIMARY_ID>SRS654517</PRIMARY_ID>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
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        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
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          <SINGLE/>
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        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA from the all samples was extracted with TRIzol reagent (Invitrogen, 15596-026) following the manufacturer’s protocol. Small RNA libraies were constructed by TruSeq Small RNA Sample Prep Kit (Illumina) following the manufacturer’s instructions. Briefly, 1 µg total RNA or purified small RNA was ligated with 3’ and 5’ adaptors and used as a template for RT-PCR. After PCR amplification, 6 µL of each sample were pooled and separated on a 6% polyacrylamide Gel. Gel slices corresponding to ~18-26 nt small RNAs were recovered.</LIBRARY_CONSTRUCTION_PROTOCOL>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina Genome Analyzer II</INSTRUMENT_MODEL>
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      <EXPERIMENT_LINK>
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      <PRIMARY_ID>SRX647215</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1428530</SUBMITTER_ID>
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    <TITLE>GSM1428530: 9058; Zea mays; ncRNA-Seq</TITLE>
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        <PRIMARY_ID>SRP044085</PRIMARY_ID>
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          <PRIMARY_ID>SRS654518</PRIMARY_ID>
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        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
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          <SINGLE/>
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        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA from the all samples was extracted with TRIzol reagent (Invitrogen, 15596-026) following the manufacturer’s protocol. Small RNA libraies were constructed by TruSeq Small RNA Sample Prep Kit (Illumina) following the manufacturer’s instructions. Briefly, 1 µg total RNA or purified small RNA was ligated with 3’ and 5’ adaptors and used as a template for RT-PCR. After PCR amplification, 6 µL of each sample were pooled and separated on a 6% polyacrylamide Gel. Gel slices corresponding to ~18-26 nt small RNAs were recovered.</LIBRARY_CONSTRUCTION_PROTOCOL>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina Genome Analyzer II</INSTRUMENT_MODEL>
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      <EXPERIMENT_LINK>
        <URL_LINK>
          <LABEL>GEO Sample GSM1428530</LABEL>
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      <PRIMARY_ID>SRX647216</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1428531</SUBMITTER_ID>
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    <TITLE>GSM1428531: Lingdan 20; Zea mays; ncRNA-Seq</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP044085</PRIMARY_ID>
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      <SAMPLE_DESCRIPTOR accession="SRS654519">
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          <PRIMARY_ID>SRS654519</PRIMARY_ID>
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          <SINGLE/>
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        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA from the all samples was extracted with TRIzol reagent (Invitrogen, 15596-026) following the manufacturer’s protocol. Small RNA libraies were constructed by TruSeq Small RNA Sample Prep Kit (Illumina) following the manufacturer’s instructions. Briefly, 1 µg total RNA or purified small RNA was ligated with 3’ and 5’ adaptors and used as a template for RT-PCR. After PCR amplification, 6 µL of each sample were pooled and separated on a 6% polyacrylamide Gel. Gel slices corresponding to ~18-26 nt small RNAs were recovered.</LIBRARY_CONSTRUCTION_PROTOCOL>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina Genome Analyzer II</INSTRUMENT_MODEL>
      </ILLUMINA>
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    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <URL_LINK>
          <LABEL>GEO Sample GSM1428531</LABEL>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX647217</PRIMARY_ID>
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    <TITLE>GSM1428532: 87-1; Zea mays; ncRNA-Seq</TITLE>
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        <PRIMARY_ID>SRP044085</PRIMARY_ID>
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          <SINGLE/>
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        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA from the all samples was extracted with TRIzol reagent (Invitrogen, 15596-026) following the manufacturer’s protocol. Small RNA libraies were constructed by TruSeq Small RNA Sample Prep Kit (Illumina) following the manufacturer’s instructions. Briefly, 1 µg total RNA or purified small RNA was ligated with 3’ and 5’ adaptors and used as a template for RT-PCR. After PCR amplification, 6 µL of each sample were pooled and separated on a 6% polyacrylamide Gel. Gel slices corresponding to ~18-26 nt small RNAs were recovered.</LIBRARY_CONSTRUCTION_PROTOCOL>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina Genome Analyzer</INSTRUMENT_MODEL>
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      <EXPERIMENT_LINK>
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          <SINGLE/>
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        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA from the all samples was extracted with TRIzol reagent (Invitrogen, 15596-026) following the manufacturer’s protocol. Small RNA libraies were constructed by TruSeq Small RNA Sample Prep Kit (Illumina) following the manufacturer’s instructions. Briefly, 1 µg total RNA or purified small RNA was ligated with 3’ and 5’ adaptors and used as a template for RT-PCR. After PCR amplification, 6 µL of each sample were pooled and separated on a 6% polyacrylamide Gel. Gel slices corresponding to ~18-26 nt small RNAs were recovered.</LIBRARY_CONSTRUCTION_PROTOCOL>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina Genome Analyzer</INSTRUMENT_MODEL>
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      <EXPERIMENT_LINK>
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          <LABEL>GEO Sample GSM1428533</LABEL>
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      <PRIMARY_ID>SRX647219</PRIMARY_ID>
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    <TITLE>GSM1428534: Yuyu 22; Zea mays; ncRNA-Seq</TITLE>
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        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA from the all samples was extracted with TRIzol reagent (Invitrogen, 15596-026) following the manufacturer’s protocol. Small RNA libraies were constructed by TruSeq Small RNA Sample Prep Kit (Illumina) following the manufacturer’s instructions. Briefly, 1 µg total RNA or purified small RNA was ligated with 3’ and 5’ adaptors and used as a template for RT-PCR. After PCR amplification, 6 µL of each sample were pooled and separated on a 6% polyacrylamide Gel. Gel slices corresponding to ~18-26 nt small RNAs were recovered.</LIBRARY_CONSTRUCTION_PROTOCOL>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina Genome Analyzer</INSTRUMENT_MODEL>
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      <EXPERIMENT_LINK>
        <URL_LINK>
          <LABEL>GEO Sample GSM1428534</LABEL>
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        </URL_LINK>
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