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vishakh82

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I think I understand what you’re saying.

We’re focusing on an incremental improvement.

There are people actively working on private home sequencing, at home analysis devices, etc and they’re best placed to do it.

We’re trying to get ahead of a near future where people, implicitly or explicitly, are paid for their genetic data in insecure or exploitative ways.

Let people get their DNA sequenced without giving up anonymity or privacy.

Let people benefit from DNA data analysis without the data leaving their device or sphere of control.

Let people monetize their genetic data without compromising their security.

We have shown that we can batch user samples and then send them anonymously to the lab. Users can then use an MPC protocol to securely fetch their data without losing anonymity.

We plan to roll out a product called Batcher which does this soon.

You're right, most analyses are done using biobanks, etc right now. The sentence is an oversimplification but people still implicitly contribute their data to insecure and centralized sources.

If we can enable people to get sequenced not just when they are sick but for altruistic or financial reasons without leaking their DNA data, we could unlock much bigger datasets than currently available, especially from populations that are underrepresented or ignored.

There are many motivations for consumer genomics and they might pick up further.

https://vishakh.blog/2025/07/08/using-mpc-for-anonymous-and-...

If you look at a previous experiment we did, the costs for getting genotyped are pretty moderate (<$80) and going down further. Blended genome-exome (<$150) and full genome sequencing (<$500) are getting cheaper as well.

Through our Explorer product (https://explorer.monadicdna.com/) we let people glean information about their genome using GWAS Catalog data.

This PoC addresses the next step, i.e. how to keep genetic data private at the user level while still allowing aggregate studies to happen, with or without financial incentives.

Hi, I’m a member of the Monadic DNA team.

This post describes a local-first approach to personal genomics. Large-scale analysis (processing raw genotype data against the GWAS Catalog, >1M traits) runs entirely on the user’s device.

LLMs are used only for exploration and summarization of selected results and they never see raw genetic data. Users can choose different LLM backends depending on their preferences, including a TEE-based option ( nilAI), local models via Ollama, or hosted models via HuggingFace.

Happy to answer technical questions about the pipeline, privacy tradeoffs, or limitations.

You may wish to build a protocol where third parties can asynchronously operate on user data. You may also want to have separation between the end app and the compute layer for legal or practical purposes. Finally, you may not want to store large payloads on client devices.

We address this point in the article. On the default path with existing rules and regulations some degree of trust in labs will always be required.

At-home sequencing could be a game changer.

The other reply also mentions molecular cryptography which could provide really strong anonymity and privacy guarantees. We hope to do a PoC accordingly some time in the neat future.

Not at all. "S3" is only in the loop because that's what labs generally use. In production, when we have ongoing scale, we will not use S3 or anything like it to transfer data between labs and our infra, even if it means using sneakernet!

The whole point of our project is to keep people's data always under encryption so that nobody can sell the data even if they wanted to. Using MPC (and FHE) we ensure that nobody can decrypt your data without your permission.

You can also delete your data any time without needing any third party's permission using the latest versions of the libraries we use.

We are building all this go get away from the closed, exploitative model that 23andMe built. The way we are building our infra, our company could go out of business tomorrow and you'll still be able to use the protocol and have access to your data and insights.

Also, fun fact, genetic data from newborns is retained by the state in many industrialized countries. We need to get that data away from "trust me, bro" infrastructure to securing it using MPC and FHE.

You're right about "anonymized" and "anonymous". We do point out avenues to reach anonymity.

The legalese is for informed consent since biological materials are involved, handling liability and pointing out that the exercise itself was experimental and an early step towards productionzation.

The physical token could be a UX nightmare and it could get expensive at scale. Using a more developed app which accept revocable public keys from the user might be more workable.

Think monad as in philosophy, less monad as in a programming burrito.

Our intention is to let each user be a self-contained, enclosed (through encryption) unit where they get insights tailored to their unique genome. At the same time, we want to aggregate data (securely and with consent) from all users to power medical and research findings.

It sort of also works in the programming monad sense as the data is always enclosed and encrypted and never "directly" operated on.

https://monadicdna.com

Open, secure personal genomics using fully homomorphic encryption.

With 23andMe bankrupt, I want to put out somewhere secure people can put their genomic data and receive insights. In a few months, I'll have a protocol in place to open up the data to third party apps (with user consent). The data does not have to be decrypted ever to be operated upon!

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