Evidence Input
Integration of OpenTargets, GWAS, CTD, PharmGKB, and CPIC data to establish a high-confidence, pharmacogenomically-annotated evidence base.
PanAum's pipeline ensures every step flows logically from initial evidence collection to a final executive-ready report, with no manual handoffs and full scientific provenance at each stage. The PGx layer runs as an integrated track with bidirectional data exchange throughout.
Integration of OpenTargets, GWAS, CTD, PharmGKB, and CPIC data to establish a high-confidence, pharmacogenomically-annotated evidence base.
Building the biological framework via STRING network construction and pathway enrichment analysis, with drug-response SNPs overlaid on the target network.
Determining the most promising therapeutic nodes via hub-gene scoring, multi-criteria ranking, and population-level allele frequency stratification across global ancestries.
Enhancing drug candidate quality through target annotation, variant-aware druggability screening across polymorphic protein conformations, and known-drug comparisons.
De novo scaffold generation using the Generative Fusion Engine with in-loop ADMET filtering and CYP/UGT/transporter polymorphism constraints embedded directly into the generation process.
Consolidating intelligence into structured final reports, executive summaries, PGx biomarker profiles, and Companion Diagnostic briefs for clinical decision-making.
Integrated PGx Track. The Pharmacogenomics layer runs alongside every stage with bidirectional data exchange — population-level variant intelligence informs target scoring, scaffold generation, ADMET constraints, and the final Companion Diagnostic brief simultaneously.
Read about the Generative Fusion Engine, In-Loop ADMET, Causal Target Validation, AlphaFold3 integration, and the Pharmacogenomics (PGx) Engine.
Core Technologies →