SparkPGx
Precision medicine starts with the right data. Process genetic test results, analyze drug-gene interactions, and generate actionable pharmacogenomic reports for prescribers.
Pharmacogenomics, Made Actionable
Genetic Test Processing
Ingest and process raw genetic test data from leading genotyping platforms. Automated variant calling, allele assignment, and phenotype interpretation built in.
Personalized Medication Reports
Generate clear, provider-friendly reports that map each patient's genetic profile to medication recommendations, dosing guidance, and alternative therapies.
Drug-Gene Interaction Engine
Comprehensive drug-gene interaction database covering major pharmacogenes. Flag high-risk interactions, provide clinical annotations, and link to CPIC guideline recommendations.
Secure & Compliant
HIPAA-compliant infrastructure with full audit trails for genetic data handling. Role-based access controls and encrypted data storage for sensitive genomic information.
Your Workflow, Your Way
SparkPGx is designed as a flexible platform that adapts to how pharmacogeneticists actually work. Configure every layer of the reporting pipeline — from gene panels to final deliverables — without writing code or waiting on vendor updates.
Custom Gene Panels
Go beyond the standard pharmacogene set. Add, remove, or reconfigure gene panels to match your laboratory's testing scope — whether you're focused on a targeted cardiology panel or a comprehensive multi-specialty assay.
Custom Allele Definitions
Define and manage star allele nomenclature on your terms. Import established allele definitions or create custom entries to capture novel or population-specific variants that standard databases may not yet include.
Configurable Clinical Guidance
Tailor drug-gene interaction recommendations to align with your institution's formulary and clinical protocols. Map phenotype-to-recommendation logic using CPIC, DPWG, or your own internal guidelines — and update them as the evidence evolves.
Report Styling & Branding
Control every aspect of your report output. Apply your laboratory's branding, customize layout templates, adjust terminology for your audience, and export in multiple formats — PDF, HL7, or structured data for downstream integration.
Built for Precision Medicine
Multi-Panel Support
Run comprehensive PGx panels covering cardiology, psychiatry, oncology, pain management, and more — all from a single platform.
EHR Integration
Deliver PGx results directly into electronic health records via HL7 and FHIR interfaces for seamless clinical decision support.
Prescriber Portal
Give ordering providers secure access to patient PGx profiles, interaction alerts, and downloadable reports through a dedicated portal.
Designed for Your Workflow
Clinical Laboratories
Labs running PGx panels who need streamlined processing, automated interpretation, and compliant reporting at scale.
Prescribers & Clinicians
Physicians and pharmacists who need actionable, evidence-based medication guidance tied to individual patient genetics.
Health Systems & Networks
Organizations implementing precision medicine programs who need enterprise-scale PGx infrastructure with EHR integration.
See SparkPGx in Action
Schedule a personalized demo to see how our pharmacogenomics platform can support your precision medicine workflows.