Welcome to PGx ToolKit
A cloud-based pharmacogenomics platform for translating genotype data into actionable clinical insights.
Variant Calling
Automated mapping of pharmacogenomic variants from VCF, genotyping arrays, and other formats.
Genotype-to-Phenotype
Map diplotype calls into metabolizer phenotypes aligned with CPIC guidelines.
Report Generation
Produce clinical-grade PDF reports with customizable templates and stylesheets.
Pipeline Automation
End-to-end batch processing with folder monitoring, HL7 integration, and API access.
Use Sign in at the top right to get started, or click here to learn more about the PGx Toolkit.