Let’s democratise access to Genomic Sequencing
Let’s democratise access to Genomic Sequencing
Let’s democratise access to Genomic Sequencing
Brought to you by the following partners
DEPT®/Health
DEPT®/Health
Digital health product development with care.
Digital health product development with care.
Amazon Web Services
Amazon Web Services
On-demand cloud computing web services.
On-demand cloud computing web services.
Datapult, an APHL Company
Datapult, an APHL Company
A secure, cloud-based, Public Health sanctioned service.
On-demand cloud computing web services.
Wisconsin State Laboratory of Hygiene
Wisconsin State Laboratory of Hygiene
Wisconsin’s Public, Environmental and Occupational Health Laboratory Since 1903
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.
Open source for all.
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.
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.
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.
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.
In the news
In the news
Let's get started
Let's get started
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.
Not a tech wizard? Not a problem. Drop us a message and we’ll help onboard your lab with the future of genomic research.