Features
Polygenic risk score (PRS) modeling
Disease risk prediction and detection
Population genetics analysis
Reduce sequencing costs by 50-90%
Eliminate bespoke software pipelines
Accelerate research timelines
Secure genetics data processing
Machine learning integration
Collaborative research platform
SaaS-based workflow (no local install)
Proprietary Recursion OS platform for drug discovery
Automated wet lab generating millions of cell experiments per week
Over 50 petabytes of biological and chemical data
NVIDIA BioHive-2 supercomputer for AI model training
Hit identification to IND-enabling studies with improved speed and cost
Potential first-in-class treatments in oncology and rare diseases
Advanced pipeline with phase 1/2/3 clinical trials (REC-4881, REC-3565)
Target identification and validation using machine learning
Generative AI for molecule design and optimization
De-identified patient data integration for precision medicine
Strategic partnerships with pharma and tech leaders
End-to-end drug development capability from preclinical to pivotal studies
Fit-for-purpose dataset generation including ADME and safety profiling
Real-world evidence generation through clinical trials
Continuous feedback loop from experiments into AI models
