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      <PRIMARY_ID>SRX467487</PRIMARY_ID>
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    <TITLE>GSM1324048: FLM; Laccaria bicolor; RNA-Seq</TITLE>
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        <PRIMARY_ID>SRP036860</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA237653</EXTERNAL_ID>
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      <SAMPLE_DESCRIPTOR accession="SRS555107">
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          <PRIMARY_ID>SRS555107</PRIMARY_ID>
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        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
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          <SINGLE/>
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        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted using the RNAeasy kit (Qiagen) as per the manufacturer's instructions with the addition of 20 mg PEG8000/mL to the extraction RLC buffer solution and an on-column DNA digestion step with DNAse I (Qiagen). RNA qualityb was verified by Experion HighSens capillary gels (Bio-Rad). Four total RNA preparations were pooled and amplified using the SMARTer PCR cDNA Synthesis Kit (Clontech) according to the manufacturer's instructions. cDNA libraries were prepared for sequencing using standard Illumina protocols by IGA Technology services (Udine,Italy)</LIBRARY_CONSTRUCTION_PROTOCOL>
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        <INSTRUMENT_MODEL>Illumina Genome Analyzer IIx</INSTRUMENT_MODEL>
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          <ID>301324048</ID>
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        <TAG>GEO Accession</TAG>
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      <PRIMARY_ID>SRX467488</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1324051</SUBMITTER_ID>
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    <TITLE>GSM1324051: Con 2w; Populus trichocarpa; RNA-Seq</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP036860</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA237653</EXTERNAL_ID>
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          <PRIMARY_ID>SRS555108</PRIMARY_ID>
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        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
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        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted using the RNAeasy kit (Qiagen) as per the manufacturer's instructions with the addition of 20 mg PEG8000/mL to the extraction RLC buffer solution and an on-column DNA digestion step with DNAse I (Qiagen). RNA qualityb was verified by Experion HighSens capillary gels (Bio-Rad). Four total RNA preparations were pooled and amplified using the SMARTer PCR cDNA Synthesis Kit (Clontech) according to the manufacturer's instructions. cDNA libraries were prepared for sequencing using standard Illumina protocols by IGA Technology services (Udine,Italy)</LIBRARY_CONSTRUCTION_PROTOCOL>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina Genome Analyzer IIx</INSTRUMENT_MODEL>
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          <DB>gds</DB>
          <ID>301324051</ID>
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      <PRIMARY_ID>SRX467489</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1324053</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1324053: ECM 2w; Populus trichocarpa; Laccaria bicolor; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP036860">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP036860</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA237653</EXTERNAL_ID>
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      <SAMPLE_DESCRIPTOR accession="SRS555109">
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          <PRIMARY_ID>SRS555109</PRIMARY_ID>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted using the RNAeasy kit (Qiagen) as per the manufacturer's instructions with the addition of 20 mg PEG8000/mL to the extraction RLC buffer solution and an on-column DNA digestion step with DNAse I (Qiagen). RNA qualityb was verified by Experion HighSens capillary gels (Bio-Rad). Four total RNA preparations were pooled and amplified using the SMARTer PCR cDNA Synthesis Kit (Clontech) according to the manufacturer's instructions. cDNA libraries were prepared for sequencing using standard Illumina protocols by IGA Technology services (Udine,Italy)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina Genome Analyzer IIx</INSTRUMENT_MODEL>
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          <DB>gds</DB>
          <ID>301324053</ID>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
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      <PRIMARY_ID>SRX467490</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1324055</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1324055: Con 4w; Populus trichocarpa; RNA-Seq</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP036860</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA237653</EXTERNAL_ID>
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      <SAMPLE_DESCRIPTOR accession="SRS555111">
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          <PRIMARY_ID>SRS555111</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN02630927</EXTERNAL_ID>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted using the RNAeasy kit (Qiagen) as per the manufacturer's instructions with the addition of 20 mg PEG8000/mL to the extraction RLC buffer solution and an on-column DNA digestion step with DNAse I (Qiagen). RNA qualityb was verified by Experion HighSens capillary gels (Bio-Rad). Four total RNA preparations were pooled and amplified using the SMARTer PCR cDNA Synthesis Kit (Clontech) according to the manufacturer's instructions. cDNA libraries were prepared for sequencing using standard Illumina protocols by IGA Technology services (Udine,Italy)</LIBRARY_CONSTRUCTION_PROTOCOL>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina Genome Analyzer IIx</INSTRUMENT_MODEL>
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  <EXPERIMENT alias="GSM1324056" accession="SRX467491">
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      <PRIMARY_ID>SRX467491</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1324056</SUBMITTER_ID>
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    <TITLE>GSM1324056: ECM 4w; Populus trichocarpa; Laccaria bicolor; RNA-Seq</TITLE>
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        <PRIMARY_ID>SRP036860</PRIMARY_ID>
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      <SAMPLE_DESCRIPTOR accession="SRS555110">
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          <PRIMARY_ID>SRS555110</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN02630931</EXTERNAL_ID>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted using the RNAeasy kit (Qiagen) as per the manufacturer's instructions with the addition of 20 mg PEG8000/mL to the extraction RLC buffer solution and an on-column DNA digestion step with DNAse I (Qiagen). RNA qualityb was verified by Experion HighSens capillary gels (Bio-Rad). Four total RNA preparations were pooled and amplified using the SMARTer PCR cDNA Synthesis Kit (Clontech) according to the manufacturer's instructions. cDNA libraries were prepared for sequencing using standard Illumina protocols by IGA Technology services (Udine,Italy)</LIBRARY_CONSTRUCTION_PROTOCOL>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina Genome Analyzer IIx</INSTRUMENT_MODEL>
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          <ID>301324056</ID>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
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  <EXPERIMENT alias="GSM1324058" accession="SRX467492">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX467492</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1324058</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1324058: Con 12w; Populus trichocarpa; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP036860">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP036860</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA237653</EXTERNAL_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS555112">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS555112</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN02630930</EXTERNAL_ID>
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      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted using the RNAeasy kit (Qiagen) as per the manufacturer's instructions with the addition of 20 mg PEG8000/mL to the extraction RLC buffer solution and an on-column DNA digestion step with DNAse I (Qiagen). RNA qualityb was verified by Experion HighSens capillary gels (Bio-Rad). Four total RNA preparations were pooled and amplified using the SMARTer PCR cDNA Synthesis Kit (Clontech) according to the manufacturer's instructions. cDNA libraries were prepared for sequencing using standard Illumina protocols by IGA Technology services (Udine,Italy)</LIBRARY_CONSTRUCTION_PROTOCOL>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina Genome Analyzer IIx</INSTRUMENT_MODEL>
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          <DB>gds</DB>
          <ID>301324058</ID>
          <LABEL>GSM1324058</LABEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1324058</VALUE>
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  <EXPERIMENT alias="GSM1324059" accession="SRX467493">
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      <PRIMARY_ID>SRX467493</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1324059</SUBMITTER_ID>
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    <TITLE>GSM1324059: ECM 12w; Populus trichocarpa; Laccaria bicolor; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP036860">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP036860</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA237653</EXTERNAL_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS555113">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS555113</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN02630932</EXTERNAL_ID>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted using the RNAeasy kit (Qiagen) as per the manufacturer's instructions with the addition of 20 mg PEG8000/mL to the extraction RLC buffer solution and an on-column DNA digestion step with DNAse I (Qiagen). RNA qualityb was verified by Experion HighSens capillary gels (Bio-Rad). Four total RNA preparations were pooled and amplified using the SMARTer PCR cDNA Synthesis Kit (Clontech) according to the manufacturer's instructions. cDNA libraries were prepared for sequencing using standard Illumina protocols by IGA Technology services (Udine,Italy)</LIBRARY_CONSTRUCTION_PROTOCOL>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina Genome Analyzer IIx</INSTRUMENT_MODEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1324059</VALUE>
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