Unsupervised gene expression analyses identify IPF-severity correlated signatures, associated genes and biomarkers
Abstract Background Idiopathic Pulmonary Fibrosis (IPF) is a fatal fibrotic lung disease occurring predominantly in middle-aged and older adults.The traditional diagnostic classification of IPF is based on clinical, radiological, and histopathological features.However, the considerable heterogeneity in IPF presentation suggests that differences in