Technical architecture
Sample-to-report, end-to-end.
Clinical-grade short-read sequencing in a European laboratory in Denmark. 200M+ variants imputed at 99.9% accuracy. Reports delivered into the clinical dashboard with full ACMG-aligned annotations.
Sample-to-report pipeline.
Collection
Clinical-grade DNA kit, blood or saliva, chain-of-custody tracking.
Sequencing
Clinical-grade short-read sequencing at 30× WGS depth in a European laboratory in Denmark.
Imputation
200M+ variants imputed at 99.9% accuracy from genotyping or low-coverage input.
Annotation & PRS
650+ polygenic models, ACMG-aligned variant classification, evidence-database linkage.
Clinical dashboard
Encrypted delivery into the physician’s portal with prioritized recommendations.
Platform specifications at a glance.
Security and compliance posture.
GDPR-compliant by design
Personal data processed and stored in the European Union. Patient consent, access logging, and data-subject rights handled per the General Data Protection Regulation.
EU data residency
Raw sequencing data, intermediate files, and clinical reports remain within EU jurisdiction. No cross-border transfer of patient-identifying genomic data.
Encrypted transport and storage
All data in transit encrypted via TLS; data at rest encrypted with industry-standard ciphers. Role-based access for every authorized user.
Audit-trail logging
Every report access, modification, and disclosure is logged for the hospital’s compliance and clinical-governance review.