Talk to us

Clinical Reporting Services

Turning Genomic Data into
Ready-to-Use Clinical Reports

Not every lab has the time, resources, or trained manpower to interpret genomic data. That’s why we offer Clinical Reporting as a Service, powered by our TWINE ecosystem. You share your sequencing outputs (VCFs or raw data), and our team delivers clinically validated, reproducible reports tailored to your needs.

➤
➤
➤
➤
Data Submission Data Submission
Final Report Final Report Delivery
Expert Review Expert Review
Automation Automated Processing

Secure upload of VCFs or raw sequencing data.

Standardized pipelines transform data into clinically interpretable variants.

Our geneticists and bioinformaticians validate flagged variants.

Clear, reproducible reports, ready for clinicians and diagnostic use.

What it means for you

Application Compatibility

Rapid Turnaround

Reports in hours, not days.

Faster Generation Time

Standardization

Reports aligned with ACMG/AMP and other global guidelines.

AI enhanced Interpretation

Expertise-on-Demand

Clinical geneticists and analysts review every case.

Accurate Interpretation

Scalability

Handle single cases or thousands of samples seamlessly.

Service Models We Offer

Basic Clinical Reporting

Automated variant annotation + clinical-grade reports.

Gene add-on Customization

Expert review of variants, including rare/complex cases.

Custom Reporting Solutions

Tailored disease panels, multi-omics integration, or institution-specific formats.