<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY center_name="GEO" alias="GSE186067" accession="SRP341941">
    <IDENTIFIERS>
      <PRIMARY_ID>SRP341941</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject" label="primary">PRJNA772277</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSE186067</EXTERNAL_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>Characterization of nucleocapsid-RNA interactions in Rift Valley fever virus infected cells</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Transcriptome Analysis"/>
      <STUDY_ABSTRACT>Crosslinking immunoprecipitation and sequencing was used to characterize nucleocapsid-RNA interactions in Rift Valley fever virus infection. This data set includes illumina HiSeq paired-end reads of Rift Valley fever virus infected HEK293 cells. The sequencing libraries were generated from nucleocapsid-bound RNAs. Overall design: Samples are prepared at 12-, 24-, and 36-hour post-infection. Each timepoint included two biological replicates of experimental treatment and one size-matched control.</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>GSE186067</CENTER_PROJECT_NAME>
    </DESCRIPTOR>
    <STUDY_LINKS>
      <STUDY_LINK>
        <XREF_LINK>
          <DB>pubmed</DB>
          <ID>34960686</ID>
        </XREF_LINK>
      </STUDY_LINK>
    </STUDY_LINKS>
  </STUDY>
</STUDY_SET>
