Genetic Test Processing
Ingest and process raw genetic test data from leading genotyping platforms. Automated variant calling, allele assignment, and phenotype interpretation built in.
Pharmacogenomics Reporting
SparkPGx
Precision medicine starts with the right data. Process genetic test results, analyze drug-gene interactions, and generate actionable pharmacogenomic reports for prescribers.
Key Benefits
Pharmacogenomics, Made Actionable
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.
Built for Pharmacogeneticists
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.
Custom Allele Definitions
Define and manage star allele nomenclature on your terms. Import established allele definitions or create custom entries.
Configurable Clinical Guidance
Tailor drug-gene interaction recommendations to align with your institution's formulary and clinical protocols.
Report Styling & Branding
Control every aspect of your report output. Apply your laboratory's branding, customize layout templates, and export in multiple formats.
Features Overview
Built for Precision Medicine
Multi-Panel Support
Run comprehensive PGx panels covering cardiology, psychiatry, oncology, pain management, and more.
EHR Integration
Deliver PGx results directly into electronic health records via HL7 and FHIR interfaces.
Prescriber Portal
Give ordering providers secure access to patient PGx profiles, interaction alerts, and downloadable reports.
Who It's For
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.
SparkPGx FAQ
Answers for Laboratory Teams
What is SparkPGx?
SparkPGx is Lab Dynamo’s platform for pharmacogenomics result processing, interpretation, and reporting.
What can be configured in SparkPGx?
Supported projects may configure gene panels, allele definitions, clinical guidance, report styling, user roles, and downstream integration according to the laboratory’s validated workflow.
Who uses SparkPGx?
SparkPGx is designed for clinical laboratories, pharmacogeneticists, prescribers, pharmacists, and health systems implementing pharmacogenomics services.
See SparkPGx in Action
Schedule a personalized demo to see how our pharmacogenomics platform can support your precision medicine workflows.