Clinical application workflows for clinical labs
Fast, reliable pathogen detection for modern diagnostics
Genome Detective streamlines NGS-based diagnostics - from raw reads to actionable, interpretable reports - in minutes. Designed for clinical laboratories that demand accuracy and speed, our platform empowers your team to detect, subtype, and characterize pathogens confidently.
By combining automation with intuitive reporting, Genome Detective helps hospital laboratories, clinical diagnostic labs and reference labs make faster research decisions, reduce workload, and maintain high-quality standards.
Genome Detective is for Research Use Only (RUO). Not for use in diagnostic procedures.
Key benefits
Automatic identification and typing of viruses, bacteria, fungi, and parasites within a single workflow.
Process raw sequencing data (FASTQ files) into ready-to-use reports in minutes, not hours.
Clear, visual reports and tables highlight clinically relevant mutations, resistance markers, and pathogen subtypes.
Pin your lab-validated version of Genome Detective to ensure analyses are consistent and reproducible across runs.
Compatible with all sequencing platforms, including Illumina, Oxford Nanopore Technologies and Sanger sequencing, supporting both high-throughput and smaller-scale diagnostics.
Full audit trails and secure data management to support lab governance and compliance requirements.
Use cases
Rapid pathogen identification
Monitoring antimicrobial resistance markers
Streamlining routine NGS diagnostics workflows
Without increasing staff burden.
Why it matters
By delivering faster, accurate results, Genome Detective helps labs optimize throughput, and reduce operational costs. Its ready-to-use platform eliminates bottlenecks in bioinformatics analysis, enabling labs to focus on interpretation and clinical decisions rather than data processing.
Case studies & testimonials