Try our interactive API demo for analyzing whole-genome (WGS) VCF files. Genetase is powered by an established local analysis pipeline that combines multiple annotation databases with automated prioritization to identify high-impact rare variants. Validated using real human WGS/VCF datasets. Explore the demo, share feedback, and gain early access to upcoming cloud features and exclusive discounts for early adopters.
*Based on Ryzen 7, 32GB RAM. Cloud version estimated (64 threads, ~85% efficiency)*
Developed with Scientific Rigor in Mind
Our platform combines cutting-edge algorithms with an intuitive interface to accelerate your genomic research.
Streamlined pipelines for processing full WGS VCF files with visualization and comprehensive annotation.
Learn moreSummarizes likely high-impact variants and why they were prioritized. Explore the interactive browser for full annotations.
Learn moreProcess and analyze variants in real-time with optimized cloud infrastructure.
Learn moreOur platform prioritizes security with encryption, access controls, and safe handling of genomic data.
Learn moreIntegrate our analysis pipeline directly into your existing workflows with upcoming RESTful APIs.
Learn moreGain early access to Genetase’s powerful API and be among the first to integrate advanced rare variant analysis into your workflow.