Get research-grade insights for your cases using state of the art agentic AI grounded in DNA and other biological data*.
*All information uploaded to Bystro must be de-identified. Bystro is intended for research, educational, and informational purposes only.
See how you can use grounded AI for case-level analysis.
Family Trio Investigation
Analyze parent-child trios to identify de novo mutations. The platform filters inherited variants, highlights candidate pathogenic mutations, and provides clinical annotations in natural language.
Phenotype-Driven Analysis
Start with a phenotype and explore relevant genetic variants. Ask questions in plain language about metabolic pathways, drug metabolism, or disease associations.
Upload standard genomic file formats from any sequencing platform or genotyping array.
WGS
VCF files from complete genome sequencing
WES
VCF files from exome capture sequencing
SNP Arrays
VCF exports from genotyping platforms
Flexible Input
Contact us for custom data formats
For professionals, educators, and curious learners.
Explore variant significance and inheritance patterns when preparing case reviews.
Investigate individual cases and generate hypotheses for further study.
Learn genomics methodology hands-on with real data in classroom or self-directed settings.
Explore your genomic data for educational purposes only. Any insights should be discussed with a medical professional, as the platform does not provide medical advice.
Looking for large-scale cohort analysis or enterprise features? Contact us..
Join researchers and clinicians using grounded AI for individual genomic analysis.
This platform is designed exclusively for research, educational, and exploratory purposes. It is not intended for clinical diagnosis, treatment decisions, or direct patient care. All findings should be validated through appropriate clinical workflows and reviewed by qualified professionals.