• Genomic analysis with patients in mind

    The easy-to-use, end-to-end genomic analysis platform for clinical environments

    Discover our platform

Introducing the most advanced platform for clinical genomic analysis…

Don’t miss
a mutation

State-of-the-art bioinformatic tools that identify complex genomic events overlooked by standard bioinformatic pipelines

Increase your team’s productivity

End-to-end germline and somatic analysis solution that manages the entire process from raw data to the clinical report

Meet quality and compliance goals

Tools to help you meet your quality control and regulatory compliance goals with support for your team in their efforts

Keep your data safe and accessible

Scalable and secure architecture that simplifies data management and meets your security and confidentiality requirements

An integrated platform for all your genomic analysis needs

Perform all your genomic analyses on a unified, easy-to-use, secure platform that meets all major regulatory requirements

We support you from laboratory certification to daily operations

Our team of expert biologists and bioinformaticians provides world-class support to get your laboratory up and running and to ensure that your team gets the help it needs on a day-to- day basis. We have a dedicated program to help your team secure and maintain your laboratory certification. Once you are up and running, our support staff will work with your team to answer questions that crop up during routine analysis.

Satisfied customers

  • It’s very nice to work with SeqOne, I’d never go back to the way I was working before. I have more confidence in the accuracy of my diagnoses and can deliver them much faster.

    Anne-Sophie Lebre

    CHU Reims, France

  • SeqOne is always available to listen and help solve my issues, collaborating with us to deliver practical solutions. This makes SeqOne, in my experience, the best bioinformatic solution on the market.

    Jean-Marc Rey

    CHU Montpellier, France

A passion for detail: challenging variants

We are passionate about creating bioinformatic solutions that target hard-to-detect variants such as MNVs, Alu elements and mid-sized deletions. These challenging variants are important because research continues to discover ways in which they impact patient health. Our custom bioinformatic modules complement the industry-standard bioinformatic tools, making it possible to detect important variants that would otherwise be undetected.

SeqOne regularly publishes and shares many of its research results via the open source community.

About SeqOne

The vision uniting the SeqOne team is a desire to improve patient outcomes with improved genomic analysis. We use significant resources on research and development to ensure that our platform offers the most effective, easy-to-use solution.

This ambitious program is driven by a team of experts covering all aspects of medical genomics; from clinicians, bioinformaticians, biologists and information technology specialists to experts in algorithmics, artificial intelligence, security and big data.

Need help improving your genomic analysis process ?

We’d love to help !