Identifying potential biomarkers of idiopathic pulmonary fibrosis through machine learning analysis.
Ontology highlight
ABSTRACT: Idiopathic pulmonary fibrosis (IPF) is the most common and serious type of idiopathic interstitial pneumonia, characterized by chronic, progressive, and low survival rates, while unknown disease etiology. Until recently, patients with idiopathic pulmonary fibrosis have a poor prognosis, high mortality, and limited treatment options, due to the lack of effective early diagnostic and prognostic tools. Therefore, we aimed to identify biomarkers for idiopathic pulmonary fibrosis based on multiple machine-learning approaches and to evaluate the role of immune infiltration in the disease. The gene expression profile and its corresponding clinical data of idiopathic pulmonary fibrosis patients were downloaded from Gene Expression Omnibus (GEO) database. Next, the differentially expressed genes (D
SUBMITTER: Wu Z
PROVIDER: S-EPMC10545744 | biostudies-literature | 2023 Oct
REPOSITORIES: biostudies-literature
ACCESS DATA