What SmartADN does
- Imports sequencing files (FASTQ, VCF, BAM, Sanger AB1, CSV) up to 2 GB, with automatic quality control
- Prioritises each genetic variant with an AI pathogenicity score (a triage aid, not an ACMG classification)
- Maps relevant variants to diseases using the MONDO ontology and the OncoTree cancer classification
- Surfaces therapeutic options from CIViC, with their level of clinical evidence
- Generates a structured PDF report ready to share with the oncologist
Who it is for
Molecular biology and genetics laboratories, oncology departments, cancer centres, private clinics and cancer genomics research teams, primarily in Algeria and French-speaking countries.
Security
All traffic is encrypted over HTTPS. Each organisation has an isolated workspace with role-based access (administrator, physician), and every access is recorded in an audit log.
Pricing
Pay-per-report at 15,000 DZD, or monthly plans: Standard at 350,000 DZD (30 reports) and Premium at 600,000 DZD (60 reports). Onboarding and training are included with subscriptions.
Decision support only
SmartADN is a clinical decision-support tool. All results must be reviewed and validated by a qualified healthcare professional.