Genetic test processing
Ingest supported testing data, apply configured variant and allele logic, and organize phenotype interpretation.
A configurable pharmacogenomics platform for processing genetic test results, interpreting drug-gene relationships, and producing actionable reports for clinical use.
Ingest supported testing data, apply configured variant and allele logic, and organize phenotype interpretation.
Generate provider-facing reports that connect a patient’s genetic findings with configured medication guidance and supporting context.
Manage gene panels, allele definitions, clinical guidance, terminology, and report presentation according to laboratory requirements.
Support access controls, auditability, and protected deployment patterns for sensitive genomic and clinical information.
Configure targeted or broad panels around the laboratory’s testing scope and clinical service lines.
Map interpretations to CPIC, DPWG, or laboratory-approved internal guidance as the project requires.
Plan supported HL7, FHIR, portal, PDF, or structured-data delivery for downstream clinical workflows.
SparkPGx serves laboratories, prescribers, pharmacists, and health systems that need structured pharmacogenomic interpretation and reporting.
SparkPGx is Lab Dynamo’s platform for pharmacogenomics result processing, interpretation, and reporting.
Yes. Panel scope and related allele or interpretation logic can be configured around the laboratory’s validated testing service.
SparkPGx can present configured pharmacogenomic guidance. Clinical content, governance, and final use remain subject to the laboratory’s validated process and professional review.
Supported HL7 or FHIR interfaces can be evaluated according to the receiving system, data requirements, and project scope.
A useful demonstration starts with your testing menu, current systems, daily volume, reporting needs, and implementation goals.