Deriving disease modules from the compressed transcriptional space embedded in a deep autoencoder.

ABSTRACT: Disease modules in molecular interaction maps have been useful for characterizing diseases. Yet biological networks, that commonly define such modules are incomplete and biased toward some well-studied disease genes. Here we ask whether disease-relevant modules of genes can be discovered without prior knowledge of a biological network, instead training a deep autoencoder from large transcriptional data. We hypothesize that modules could be discovered within the autoencoder representations. We find a statistically significant enrichment of genome-wide association studies (GWAS) relevant genes in the last layer, and to a successively lesser degree in the middle and first layers respectively. In contrast, we find an opposite gradient where a modular protein-protein interaction signal is stron

SUBMITTER: Dwivedi SK 

PROVIDER: S-EPMC7016183 | biostudies-literature | 2020 Feb

REPOSITORIES: biostudies-literature