<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY center_name="GEO" alias="GSE216716" accession="SRP404912">
    <IDENTIFIERS>
      <PRIMARY_ID>SRP404912</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject" label="primary">PRJNA895043</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSE216716</EXTERNAL_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>Cancer cell genetics shaping of the tumor microenvironment reveals myeloid cell-centric exploitable vulnerabilities in hepatocellular carcinoma [WES]</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Other"/>
      <STUDY_ABSTRACT>Hepatocellular carcinoma (HCC) is a highly heterogenous disease associated with an equally dynamic tumor microenvironment (TME).  We generated somatic HCC mouse models bearing clinically-relevant oncogenic driver combinations that faithfully recapitulated different human HCC subclasses. Using WES data, we explored the tumor mutation frequencies between models and compared them with human datasets. Overall design: WES profiles of bulk tumors from genetically-distinct HCC mouse models. 3 biological replicates were pooled.</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>GSE216716</CENTER_PROJECT_NAME>
    </DESCRIPTOR>
  </STUDY>
</STUDY_SET>
