Let’s democratise access to Genomic Sequencing

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DEPT®/Health

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Datapult, an APHL Company

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Wisconsin State Laboratory of Hygiene

Wisconsin’s Public, Environmental and Occupational Health Laboratory Since 1903

Explore a guided prototype

Learn how Easy Genomics works and experience a guided tour of the platform.

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Open source for all.

Easy Genomics is a no-code, open-source solution for genomic data analysis. If the past few years have taught us anything, it's that genomic sequencing will play a major part in the future of (public) health. But it's an intensive, complex and expensive process to set up and run. 


We’ve changed that. 

Simple to use.

Requires little to no technical expertise.

Secure data storage

Endless scalability as your needs grow.

Start small, scale fast

Encrypted security to keep your patient data locked and secure.

Seamless experience

Powered by NextFlow, we provide a faster, hassle-free workflow.

How it works

Run your genomic workload on a no-code front-end interface, that any non-technical user can operate in three easy steps:

Select a Workflow

Customise to your analytic requirements.

Upload your Data

Manage access to single & multiple samples.

Hit Submit

Monitor & receive your results via browser or email.

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Let's get started

Not a tech wizard? Not a problem. Drop us a message and we’ll help onboard your lab with the future of genomic research.

Install it myself

Speak to an expert