<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY center_name="BioProject" alias="PRJNA769595" accession="SRP341671">
    <IDENTIFIERS>
      <PRIMARY_ID>SRP341671</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject" label="primary">PRJNA769595</EXTERNAL_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>Fusarium graminearum MAPKs triple mutant Raw sequence reads</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Other"/>
      <STUDY_ABSTRACT>The three MAPKs (Gpmk1, Mgv1, FgHog1) in Fusarium graminearum strain PH-1 were all deleted, the triple mutant showed severe growth defect on CM plate compared with the wild type. Total RNAs isolated from aerial hyphae cultured on CM medium were sequenced by Illumina HiSeq 2500 at Novogene Bioinformatics Technology (Beijing). The RNA-seq reads were mapped to the PH-1 reference genome using HISAT2 with its two-step algorithm. RNA-seq analyze helps us identify downstream genes of MAPKs.</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>Fusarium graminearum PH-1</CENTER_PROJECT_NAME>
    </DESCRIPTOR>
  </STUDY>
</STUDY_SET>
