The Clinical Genomics Platform Built for Every Step From Test Order to EHR Delivery
A complete, cloud-native clinical genomics platform managing the full genomic testing lifecycle with HIPAA-compliant architecture, ACMG variant classification workflow software, HL7 FHIR EHR integration, and automated clinical report generation.
What the Clinical Genomics Platform Does
Six integrated modules. One governed system. Every capability designed for the clinical production environment not adapted from a research tool.
Built for Clinical-Grade Reliability & Compliance
The platform runs on HIPAA-compliant cloud genomics infrastructure with end-to-end encryption, VPC isolation, immutable audit trails, engineered for deployment on AWS, GCP, or Azure. Every integration follows HL7 FHIR genomics integration standards, and every pipeline run is Kubernetes-orchestrated for auto-scaling and fault tolerance.
Platforms That Work Alongside the Clinical Genomics Platform
Frequently Asked Questions
A LIMS tracks samples and test status. NonStop's Clinical Genomics Platform connects that to NGS pipeline development services, ACMG variant classification workflow software, automated clinical report generation, HL7 FHIR EHR delivery, and patient and provider portals - in one governed, HIPAA-compliant system. It is the difference between a system of record and a system of operation. Labs using the platform replace 4–6 standalone tools with a single integrated clinical genomics platform, reducing handoff errors, compressing TAT, and entering every accreditation audit with a complete, unbroken digital audit trail.A production-ready clinical bioinformatics pipeline must be reproducible across runs, scalable for clinical sample volumes, auditable for regulatory compliance, and integrated with clinical systems such as LIMS and reporting platforms.
Yes. The platform supports configurable bioinformatics pipeline execution for germline workflows - WES and WGS with GATK HaplotypeCaller and DeepVariant and somatic workflows, including tumour-normal paired analysis, liquid biopsy panels for low-VAF detection, and oncology-specific tertiary analysis with AMP/ASCO/CAP somatic variant tiering. ACMG variant classification and somatic tiering run as separate configurable modules within the same interpretation workflow layer, so labs running both test types operate through a single unified platform rather than maintaining parallel systems. Pharmacogenomics panel workflows are also supported, including CPIC-compliant star-allele determination and pharmacogenomics CDS EHR integration for point-of-care prescribing alerts.
Ready to Replace Your Disconnected Genomics Stack with One Governed Platform?
Tell us your assay types, your current system stack, and your compliance requirements. We scope every Clinical Genomics Platform build to your exact operational context.