• Your patient's genomics are as unique as a fingerprint

    Tap into a deeper source of genomic insights with SeqOne’s revolutionary genomics analysis platform

    Discover our platform:

  • Hot news

    January 30th, 2023

    We are pleased to announce the appointment of Martin Dubuc as new Chief Executive Officer of SeqOne Genomics.

    Click here to learn more >
  • Hot news

    October 18th, 2023
    Seamless transition from Agilent Alissa Interpret to SeqOne Platform

    As Agilent's Alissa interpret will be discontinued, we've designed a smooth migration plan to move easily to SeqOne Platform.

    Learn more & start your transition >

Introducing the most advanced platform for clinical genomic analysis…

Don’t miss
a mutation

State-of-the-art bioinformatics 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

Solutions for each type of medical use

Solutions for Labs

Empower your labs to deliver a range of state-of-the-art tests with ultra-high accuracy and optimum efficiency.

Solutions for Biopharmas

Optimize your trial and market access project with fast, accurate genomic analysis and access to patient cohorts.

Using data and machine learning to build a
more accurate picture of each patient

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.

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

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 !