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Detecting the Molecular System Signatures of Idiopathic Pulmonary Fibrosis through Integrated Genomic Analysis

2 May 2017

Abstract excerpt

Idiopathic Pulmonary Fibrosis (IPF) is an incurable progressive fibrotic disease of the lungs. We currently lack a systematic understanding of IPF biology and a systems approach may offer new therapeutic insights. Here, for the first time, a large volume of high throughput genomics data has been unified to derive the most common molecular signatures of IPF. A set of 39 differentially expressed genes (DEGs) was...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 28484236
DOI: 10.1038/s41598-017-01765-6

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