
With SeqOne Flow, seamlessly integrate your lab systems and automate routine tasks from sample import to clinical reporting. Flexible deployment options and customizeable workflows mean you stay in control while accelerating genomic analysis.
With 92% specificity, SmartPick instantly suggests the most likely disease-causing variants
*Study on singleton with HPOs
Achieve diagnosis in record time with 90% of causal variants ranked in the top 3.
Validate key metrics like kinship, contamination, and sample ID before analysis, ensuring data integrity and accuracy from the start.
Comprehensive quality metrics include customizable thresholds, automated validation, clear reporting and export capabilities
Maintain quality and transparency with versioned worksets, enabling controlled development, testing, and traceable annotations.
Identify acquired mutations in cancers.
Pinpoint germline variants.
Full audit trail of all genomic analysis actions, ensuring complete documentation of your diagnostic workflow
Granular access control that aligns with your lab's roles and responsibilities
Efficiently distribute cases to team members while maintaining clear oversight of workload
Enable in-silico panel restrictions to prevent incidental findings.
Your data stays yours—never shared, never sold. Our patented double-encryption system secures each patient file with a unique key for maximum data protection. You stay safe, compliant, and in control.
The SeqOne Platform is an in vitro diagnostic medical device, CE-IVD Class C certified under IVDR. The company is certified under ISO 13485 for medical grade quality, ISO 27001-compliant, and HDS-certified for maximum data security.
Validate SeqOne with your own data, expert support, and zero commitment.
Pay-per-analysis with no hidden fees or volume constraints.
Access field specialists, multi-lingual assistance and hands-on guidance.