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Highlight variants, drugs, or genes in literature to instantly query the Darlyne Omni-Matrix. Darlyne AI is a deterministic pharmacogenomics (PGx) research companion designed to seamlessly integrate with your clinical literature workflow. Built for researchers across the PGx landscape (e.g., epidemiologists, academics, pharma scientists, etc), the Darlyne AI extension allows you to highlight any gene, drug, variant (rsID), or clinical toxicity on pages like PubMed or PubChem and instantly cross-reference it against our proprietary database. By bridging the gap between static academic journals and dynamic matrix data, Darlyne ensures your research is backed by clinically verified structural edges, eliminating the hallucinations common in standard LLMs. Key Features: Instant Matrix Queries: Highlight a clinical target, right-click, and open the Darlyne Side Panel to instantly view validated structural edges, including gene-drug interactions, clinical toxicities, biological pathways, and GTEx tissue expression. AI-Powered Synthesis: Ask natural language questions directly within the extension to receive highly objective, epidemiological summaries streaming in real-time. Contextual UI: The side panel seamlessly parses raw data into intuitive, color-coded topology components (Genes, Drugs, SNPs) without disrupting your reading flow. Tab Isolation: Built with strict clinical UX in mind, the panel is tab-specific, ensuring your research environment stays precisely where you left it. Seamless Web Integration: Effortlessly port your side-panel research directly into the full Darlyne.ai web platform with a single click. Powered by Destin Genomics.