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.
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