Decode 100% of the Genome with AI
We transform noisy data from whole genome sequencing into actionable insights covering coding and non-coding DNA.
Cutting-edge technology and precision at scale for research, drug discovery, and clinical diagnostics.
A spin-off from:
All-in-one AI powered platform for variant detection, prioritization, interpretation and data sharing
100% Genome Coverage
Fast Large-Scale Cohort Analysis
87% Fewer False Positives
Complete Variant Detection
Full Multi-Omics Integration
What we offer
Comprehensive genome analysis
Our software analyses the whole genome on cohort, family or individual level tailored to your needs.
Variation detection and ranking
Through the detection, ranking, and prioritization of mutations, you are provided with a manageable list of suggested pathogenic mutations.
Cutting edge AI Technology
Detection
High-quality detection methods that decrease false-positive structural variants by 87%, including DEL, DUP, INS and INV.
Prioritization
Disease-agnostic AI tool ranks over 80% of known pathogenic variants in the top 10. On top of that, we created a disease-specific scoring system with over 90% accuracy, it ensures precise prioritization for more reliable research outcomes.
Discover our Platform
Get a personalized walkthrough of our platform and see how it can benefit your needs.
Resources
Our latest whitepaper is out!
2025 May 28
Here we explain DICAST, a novel machine learning model that detects SVs from short-read data.
Read the paper through the link!
Episode 34 of the BioRevolution podcast
2025 May 5
Hossein was a guest at the BioRevolution podcast to talk about the new insights into the genetic basis of diseases. Listen to it through the link!
Lucid Genomics at the European Society of Human Genetics
2025 May 25
The ESHG was a great time to finally see some familiar people in person and show our latest developments to new experts
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