Pathogen identified.
45 minutes.
Nanolix runs adaptive basecalling directly on nanopore flow cell output — no cloud dependency, no latency tax — designed for clinical laboratory validation at the point of care.
Cloud callers weren't built for the bedside
Standard basecalling pipelines assume you have time. Research labs tolerate 2-4 hour cloud roundtrips because the clinical answer can wait. Hospital ICUs cannot.
The 12–15% raw error rate in nanopore sequencing is manageable in research — you run longer, average more reads. In a clinical setting, every minute of additional sequencing time is a minute before the infectious disease physician can act on your result.
Consensus-only callers aren't optimized for the error profile of clinical isolates. They were trained on reference genomes, not the diverse pathogen populations you'll see in a hospital microbiology laboratory.
Nanolix re-implements the basecalling stack from first principles: on-device, real-time, adaptive — with a pathogen-specific model library trained on clinical isolates.
From raw signal to clinical answer
Three stages. All local. Under 45 minutes.
Raw ionic current signal from Oxford Nanopore flow cell output is read in real-time as reads stream from the sequencer. No batch collection, no waiting for run completion.
On-device adaptive basecalling corrects the 12–15% raw error rate without cloud roundtrip. Context-aware model conditions on preceding bases and signal context to reduce systematic errors at homopolymer runs and modified-base-rich sequences.
Pathogen ID, AMR gene detection, and a confidence score delivered sub-45-minutes. Results formatted for direct output to your LIS via HL7 v2 or FHIR. No cloud. No data leaves your facility.
Designed for the pathogens your lab faces most
Current identification panel — continuously updated. All organisms identified from Oxford Nanopore flow cell output data.
Internal validation data
LDT-compatible architecture, designed for hospital laboratory validation workflows.
Validation data available to qualified laboratory partners. Nanolix is software — clinical validation is the responsibility of the implementing laboratory under LDT regulatory frameworks.
Runs where your sequencer runs
Complete local execution architecture. No cloud in the critical path.
Cloud node shown as optional reporting sync only — not in the critical analysis path.
Connects to your clinical workflow
Standard outputs for LIS, EHR, and LIMS environments. Zero proprietary lock-in.
Ready to bring sequencing to point-of-care?
Request access for your laboratory's evaluation. No per-run fees — one site license, unlimited runs.