A deep learning system for analyzing depression's proteomic architecture using UK Biobank data (53,000+ participants, 2,900 proteins). Implements Improved Deep Embedded Clustering with a symmetric autoencoder (d-500-500-2000-16 architecture) to investigate biological subtypes. Key findings demonstrate continuous rather than categorical protein expression patterns, with robust demographic signal detection and validation across multiple clustering approaches (PCA+k-means, UMAP+HDBSCAN). Research done with Weill Cornell Medicine under Dr. Logan Grosenick, Dr. Connor Liston, and Elias Scheer.