Research and precision medicine, now within reach for any researcher, clinician, or curious individual. Plans start at $20/mo.
Pick your plan. Start asking big questions.
Starter, Essential, or Pro for individual use. For proprietary data, petabyte-scale cohorts, or on-prem deployment, see below.
Starter
For getting started.
$20/mo
Billed monthly
Upload your genetic data and get a thorough investigation with your first question.
20 credits/mo= 1 Plus investigation/mo$1 per credit · top up anytime
Unlimited Genetics (Bystro Dash)
Upload your genetic file and access rigorous research-grade tools
Quality control metrics, automatic ancestry, PRS at the click of a button
Instantly search through your variants annotated with RefSeq, ClinVar, gnomAD, dbSNP, CADD, and more
Agentic AI (Bystro Think)
1 Plus investigation/mo
Deep research across PubMed, arXiv, ClinVar, genetic analysis, and statistical reasoning
Every finding fact-checked against primary sources
Data Storage
Included
Essential
Recommended
For the most value.
$50/mo
Billed monthly
The most comprehensive answers to your questions at your fingertips.
60 credits/mo= 3 Plus or 2 PhD investigations/mo$1 per credit · top up anytime
Unlimited Genetics (Bystro Dash)
Everything in Starter
Agentic AI (Bystro Think)
3 Plus or 2 PhD investigations/mo
Do a complete research project in a single conversation, including data processing, QC, literature review, and analysis
All compute included
Data Storage
Included
Pro
For power users.
$100/mo
Billed monthly
Keep asking all of your big questions and getting big answers.
120 credits/mo= 6 Plus or 4 PhD investigations/mo$1 per credit · top up anytime
Unlimited Genetics (Bystro Dash)
Everything in Essential
Agentic AI (Bystro Think)
6 Plus or 4 PhD investigations/mo
Extended reasoning for the hardest questions
Priority processing
Data Storage
Included
*Cross-ancestry polygenic risk scores derived from existing GWAS summary statistics — no retraining required.
Enterprise and institutions
Custom
Need multi-seat licenses, on-prem deployment, or bioinformatics support?
For labs, clinics, pharma, and research institutions. Multi-seat licenses, centralized billing, proprietary data inside your own infrastructure, and co-development on specialized workflows.
Enterprise includes
Multi-seat licenses with centralized billing and usage allocation
On-premises deployment inside your infrastructure
Data privacy controls, SAML/SSO, and audit logs
Co-development for new feature development and bioinformatics consultation
Petabyte-scale cohort analysis and custom bioinformatics pipelines
Ask anything, with or without data. Every answer is grounded, cited, and verifiable.
1
Ask a question
Start with anything, such as a variant, a diagnosis, a drug, a research question. No data required.
2
bystro searches the literature
Hundreds of agentic steps across PubMed, arXiv, ClinVar, and primary sources in minutes.
3
Your data is analyzed
If you uploaded a VCF, 23andMe file, or cohort, bystro factors it in directly.
4
Every claim is verified
Findings are cross-checked against primary sources and analyses are checked for correctness.
5
You get a cited report
A detailed, citation-backed answer you can act on with fully auditable references and analyses.
Full comparison
What's included
Starter
Essential
Pro
Enterprise
Agentic research
Investigations / mo
1 Plus
3 Plus or 2 PhD
6 Plus or 4 PhD
Custom
Credits included / mo
20 cr
60 cr
120 cr
Custom
No data required
Credit top-ups
Genetic analysis & bioinformatics
Consumer genetics (Sequencing.com, etc.)
WGS / WES annotation & QC
Polygenic risk scores
Proteomics & multi-omics
Custom analyses
Petabyte-scale cohorts
Data storage
On-premises
Platform
API access
On-premises deployment
Support
Email
Email
Priority email
Priority email + SLA
Questions & answers
All prices in USD. Billing via Stripe. Questions? team@bystro.io
Research Use Only. This platform is for research, educational, and informational purposes. Not intended for medical diagnosis, treatment, or clinical use. Always consult qualified healthcare professionals.
