SecureDNA was designed to screen all oligo and gene synthesis orders against an up-to-date list of known and emerging hazards, including pre-generated functional variants.

Diagram showing orders being split into subsequences, one-way-encrypted, and compared to an encrypted hazards database

Universal - fast, free, and available to all



Rapid and delay-free screening at thousands of base pairs / sec, plus optional customer pre-screening



Non-profit and free to use, thanks to several generous donations and our efficient exact-match algorithm

Accessible (image of globe)


Available to all providers with free integration support, to safeguard DNA synthesis worldwide

Comprehensive - sensitive, specific, and up-to-date

SecureDNA is sensitive, detecting known hazards


Detects all known hazards and predicted functional variants down to 30 b.p., preventing oligos too small to be screened by other methods from being used to assemble hazards 

Specific, outputting negligible false alarms


Outputs ~0 false alarms by using patented reverse screening to remove known non-hazards, enabling use in synthesizers and assemblers without human support

Up-to-date - picture of a clock


Uses a centralized database, updated swiftly by our biosecurity team as new threats are identified; no need to update local installations

Trustworthy - privacy-preserving and neutral

Privacy-preserving - picture of padlock on computer keyboard


Protected by multiple layers of cryptography & distributed around the world, your customers’ sequences will be uninterpretable - by us or anyone else

Swiss flag

Politically neutral

Run within a Swiss non-profit foundation without involvement by any government - a worldwide research collaboration

Detailed description of the platform

Hands of a scientist, under a sterile hood, preparing the carcinoembryonic antigen (CEA) vaccinia used to try to prevent cancer.

The SecureDNA system uses a novel exact-match search algorithm that finds matches to hazards and functional equivalents. It does this by generating the set of all hazard subsequences of a predefined length, choosing some to defend quasi-randomly, then using algorithms to generate millions of functionally equivalent subsequences of each. These are subjected to reverse screening by comparing them to existing sequence databases in order to remove any that match known non-hazardous entries.

The reverse screening step virtually eliminates false positives, the inclusion of quasi-random functional variants prevents adversaries from redesigning or mutating the hazard to evade screening, and searching for 30 base pair subsequences makes it very difficult to assemble hazards from oligonucleotides that are too small to be screened using other methods.

Because exact-match screening is computationally efficient, we can apply oblivious multi-party cryptography to protect the confidentiality of both orders and the hazard database. Using this scheme, each possible subsequence of an order to be screened is turned into a unique cryptographic hash, and each such hash is then looked up in the database of hazards.

This hash requires multiple separate machines to compute, meaning that even an attacker who could eavesdrop on network traffic or compromise a subset of computers in the screening system could not learn the plaintext of a customer order, and not even SecureDNA itself ever receives the customer’s DNA sequences—they remain safely on-premises at a provider or within the hardware of a benchtop synthesizer.

Screening for hazardous DNA sequences is provided as a free service by the SecureDNA Foundation, an independent nonprofit foundation in the sense of Article 80 et seqq. Swiss Civil Code with legal seat in Zug, Switzerland. The purpose of the Foundation is to develop, maintain, administrate, distribute, and encourage the universal adoption of software for screening nucleic acid sequences. The Foundation may support any action intended to prevent nucleic acids from being used to cause harm.

Partners and Support

We are grateful for support from the Open Philanthropy Project to team members at MIT, Aarhus University, and Northeastern University, and to an anonymous Chinese philanthropist for a donation to team members at Tsinghua University and Shanghai Jiao Tong University.

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  • 资源 2
  • Shanghai Jiao Tong University