Join the Beta - BioVault is a free and open-source tool and permissionless network for collaborative genomics

For Researchers

$ bv biobank list

✓ Listing BioBanks

$ bv run ./myproject syft://research@mybiobank#participants --test

✓ Testing NextFlow Pipeline

$ bv submit ./myproject syft://research@mybiobank#participants

⚡ Analysis Submitted

---------------------------------

$ bv inbox

Project	Status	Path
myproject	✅ Success	./myproject/results

How it works:

Find participants with variant and phenotype data for research
Submit nextflow pipelines to BioVault users or biobanks
Write nextflow pipelines with the help of AI
Perform joins between participants in different biovaults using Secure Enclaves
No need to safe guard sensitive data that is never shared

FASTQBAMCRAMVCFNextFlowPhenotype DataWearable Data

Open Network

How it works:

Variants published to relay server with public keys for anonymity
Built on SyftBox, an open-source network for secure data science
Encrypted messages via relay servers, no open ports needed
Data stays on participants' devices, only insights are shared
Collaborate without requiring data uploads to the cloud

Open SourceOpen NetworkEnd-to-end EncryptedSecure Enclaves

For Participants

How it works:

Supports common variant and raw data formats from major providers
Get free ClinVar updates for your variants without sharing data
Invite clinicians and experts to analyze your data on your computer securely

VCFs23andmeAncestryDNAMyHeritageCariGenetics.comSequencing.comDante LabsNebula

Built for the Future of Research

🔓

Open Source

Transparent, community-driven development with full access to source code

💚

Free

Apache 2.0 Licensed. No fees or hidden costs. Research should be accessible to everyone

🚀

Permissionless

Start collaborating immediately without any approval processes

🔒

Privacy First

End-to-end encryption and user-controlled data sharing

🌐

Decentralized

No single point of failure or control - true peer-to-peer research

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Secure Enclaves

Leverage state of the art secure enclaves to perform joint analysis between data without centralizing it

Beta Testers

Rare disease patients who already have access to their raw sequencing data.
Participants who have Variant data from services like 23andme, Ancestry, MyHeritage, CariGenetics.com, Sequencing.com, Dante Labs, Nebula, etc.
Researchers who want to help perform data visitation and remote data science with the platform.
Organisations or Labs with access to .
Tech enthusiasts who want to learn about Genomics and have some fun!

Frequently Asked Questions

What is BioVault?

BioVault is a platform designed to empower individuals and revolutionize research by providing a secure, decentralized, and open-source environment for genomics collaboration.

How can I join the Beta?

You can join the Beta by signing up with your email address in the signup section above. We will send you updates and early access information.

Is BioVault free to use?

Yes, BioVault is free to use under the Apache 2.0 License. We believe the fruits of genetic research should be accessible to everyone.

How does BioVault ensure privacy?

BioVault ensures privacy through end-to-end encryption and user-controlled data sharing, ensuring your data is always secure.

What is SyftBox?

SyftBox.net is an open-source network for privacy-first, offline-capable data science and AI.

How does SyftBox work?

SyftBox is designed to work everywhere including on mobile devices and home computers which can go offline at any time.

SyftBox works by sending end-to-end encrypted network messages which can be cached temporarily via relay servers, thus eliminating the need for open ports and online connections.