Genomics ships inside Biology and Drug Discovery. This page is a deep dive.
Read the genome.
Reveal the signal.
Variant effect, expression prediction, and panel support—made intuitive.
Sequencing to delivery.
One living system.
Clinical Annotation
From code to classification
Automated ACMG scoring (Pathogenic, Benign, VUS). Rule-based evidence explanation for every call. Phenotype integration.
Expert Adjudication
Human-in-the-loop confidence
Route low-confidence variants to specialists. Capture clinician notes. Maintain full audit trails for regulatory review.
Private Model
Your interpretation logic, learned
Fine-tune Nucleotide Transformer on your case history. Block regressions with concordance gates. Own the weights.
Production performance.
Measured live.
The AuraOne
difference.
Clarity
Status quo
Disconnected pipelines, manual reconciliation
With AuraOne
99.2% concordance across BWA, GATK, DeepVariant
Speed
Status quo
Days to review pathogenic variants
With AuraOne
3x faster with guided explainability
Scale
Status quo
Weeks to reprocess cohorts
With AuraOne
8.5 hours for nation-scale refresh
"I annotate a family's variant panel in AuraOne so that physicians receive an evidence-backed report within 24 hours. It's faster and safer."
Trusted by leading genomics programs