<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX4632439" alias="RNA-seq-ctrl1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4632439</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4482691">RNA-seq-ctrl1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>ISL1-Ctrl-1</TITLE>
    <STUDY_REF accession="SRP159301">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP159301</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA488860</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA was prepared using the RNeasy Micro kit (Qiagen) following the manufacturers instructions. The quality of the resulting RNA was verified by the relative intensity of rRNA bands using a Agilent 2100 Bioanalyzer, and RNA was quantified using a Nanodrop ND-1000 spectrophotometer. RNA libraries were prepared for sequencing using standard BGISEQ protocols.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3733351">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3733351</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|zqt042809">SHSY5Y_ISL1_Ctrl_rep1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RNA-seq-ctrl1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <BGISEQ>
        <INSTRUMENT_MODEL>BGISEQ-500</INSTRUMENT_MODEL>
      </BGISEQ>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
