<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY center_name="GEO" alias="GSE186652" accession="SRP343395">
    <IDENTIFIERS>
      <PRIMARY_ID>SRP343395</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject" label="primary">PRJNA774977</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSE186652</EXTERNAL_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>Next Generation Sequencing analysis of KSHV lytic replication in TREx-BCBL1-RTA cells</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Transcriptome Analysis"/>
      <STUDY_ABSTRACT>Purpose: miR-Seq was utilised to identify miRNAs which are altered during the course of KSHV lytic replication at  0, 16 and 24 hours post reactivation in TREx-BCBL1-RTA cells. Methods: Virus lytic replication was induced via addition of 2 µg/mL doxycycline hyclate (Sigma-Aldrich). Total RNA was extracted from TREx-BCBL-1s at 0, 16 and 24 hours post lytic induction. Small RNA libraries were prepared using the TruSeq Small RNA Library Prep Kit (Illumina). Quality filtered (Q &lt; 20), and adapter trimmed reads (Trimmomatic v0.39) [59] were aligned to the GRCh38/hg38 assembly of the human genome using Bowtie2 (V 2.4.2). Overall design: miRNA profiles during the course of KSHV lytic replication at  0, 16 and 24 hours post reactivation in TREx-BCBL1-RTA cells in triplicates.</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>GSE186652</CENTER_PROJECT_NAME>
    </DESCRIPTOR>
    <STUDY_LINKS>
      <STUDY_LINK>
        <XREF_LINK>
          <DB>pubmed</DB>
          <ID>35239998</ID>
        </XREF_LINK>
      </STUDY_LINK>
    </STUDY_LINKS>
  </STUDY>
</STUDY_SET>
