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      <SUBMITTER_ID namespace="LANGEBIO-CINVESTAV">L. williamsii transcriptome (GS-FLX reads)</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Mixed ranscriptomes from roots and button (tops of stems) of Lophophora williamsii</TITLE>
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        <PRIMARY_ID>SRP057967</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>Total RNA was isolated from roots and buttons using the Trizol reagent (Invitrogen) and re-purified with the RNeasy kit (Qiagen) following the manufacturer’s recommendations. RNA purity was checked using the Agilent 2100 Bioanalyzer RNA 6000 Nano Assay chip (Agilent Technologies, Stockport, U.K). cDNA synthesis was performed from 3.5 µg of total RNA using the Message Amp-II kit (Ambion, Foster City, CA) following the manufacturer’s protocol. cDNA derived from button and peyote roots was pooled (using the same amount of each) and sequencing on GS-FLX and GS-Junior platform (one run per equipment).</DESIGN_DESCRIPTION>
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  <EXPERIMENT alias="L. williamsii transcriptome (GS-Junior reads)" accession="SRX701021" center_name="LANGEBIO-CINVESTAV">
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      <PRIMARY_ID>SRX701021</PRIMARY_ID>
      <SUBMITTER_ID namespace="LANGEBIO-CINVESTAV">L. williamsii transcriptome (GS-Junior reads)</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Mixed ranscriptomes from roots and button (tops of stems) of Lophophora williamsii</TITLE>
    <STUDY_REF accession="SRP057967">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP057967</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA261064</EXTERNAL_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>otal RNA was isolated from roots and buttons using the Trizol reagent (Invitrogen) and re-purified with the RNeasy kit (Qiagen) following the manufacturer’s recommendations. RNA purity was checked using the Agilent 2100 Bioanalyzer RNA 6000 Nano Assay chip (Agilent Technologies, Stockport, U.K). cDNA synthesis was performed from 3.5 µg of total RNA using the Message Amp-II kit (Ambion, Foster City, CA) following the manufacturer’s protocol. cDNA derived from button and peyote roots was pooled (using the same amount of each) and sequencing on GS-FLX and GS-Junior platform (one run per equipment).</DESIGN_DESCRIPTION>
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  <EXPERIMENT alias="L. williamsii transcriptome (IonPGM reads)" accession="SRX701022" center_name="LANGEBIO-CINVESTAV">
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      <PRIMARY_ID>SRX701022</PRIMARY_ID>
      <SUBMITTER_ID namespace="LANGEBIO-CINVESTAV">L. williamsii transcriptome (IonPGM reads)</SUBMITTER_ID>
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    <TITLE>Transcriptomes from roots and button (tops of stems) of Lophophora williamsii specie</TITLE>
    <STUDY_REF accession="SRP057967">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP057967</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA261064</EXTERNAL_ID>
      </IDENTIFIERS>
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    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was isolated from roots and buttons using the Trizol reagent (Invitrogen) and re-purified with the RNeasy kit (Qiagen) following the manufacturer’s recommendations. RNA purity was checked using the Agilent 2100 Bioanalyzer RNA 6000 Nano Assay chip (Agilent Technologies, Stockport, U.K). cDNA synthesis was performed from 3.5 µg of total RNA using the Message Amp-II kit (Ambion, Foster City, CA) following the manufacturer’s protocol. cDNA samples were prepared with the Ion Xpress™ Template Kit (Life Technologies) according to the Ion Xpress™ Template Kit User Guide and sequenced on a Personal Genome Machine™ (PGM™) sequencer using two 3.18 semiconductor chips. The adapters used were MID01 (TCGATAATCTTCTGCTGTACGGCCAAGGCGT) and MID02 (TGATGATTGCCCTGCTGTACGGCCAAGGCGT) from roots and button, respectively)</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS701107</PRIMARY_ID>
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            <READ_INDEX>1</READ_INDEX>
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