Tool for labs · in development
AI NGS interpreter
From raw reads — to a draft report.
We are building a platform that will take sequencing data from raw reads to a draft report: processing and quality control, variant calling and annotation, ACMG/AMP classification with transparent criteria, and a literature search with a reference for every statement.
How it works
Four steps to a draft report
- Processing and quality control
- Variant calling and annotation
- ACMG/AMP classificationWith transparent criteria.
- Literature evidenceWith a reference for every statement.
This is a decision support system: the final word always belongs to the lab’s geneticist.
Key points
What matters to a lab
Designed for MGI/DNBSEQ and Russian-made sequencers
Patient data will stay in the client’s jurisdiction
A cloud in the client’s country or an on-premises installation in the lab.
Reports in Russian (English planned)
Will take Russian population allele frequencies into account
First use case
Hereditary cancer syndromes
We start with BRCA1/2 and Lynch syndrome. A research-use-only version (RUO) comes first.
In development
Waitlist for labs and pilot partners
Leave your details and I’ll write when there is something to show.
This is not a medical device and does not make a diagnosis.