True end-to-end genomic analysis

SeqOne provides a true end-to-end genomic analysis. From automated data import all the way through to detailed clinical reports and therapeutic recommendations. SeqOne manages all aspects of the process in a single integrated approach that improves accuracy, facilitates the traceability essential for lab certification while improving lab efficiency.

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

Bioinformatic apps to answer
each medical question

SeqOne’s platform features a catalog of bioinformatic applications, each optimized to answer a specific medical question. Whether you are analyzing WES or WG data to diagnose rare diseases or performing RNA analysis to recommend the right therapy for a cancer patient, you will find an app that has been designed to give you the best results. Each of our apps includes specific visualisation tools and custom bioinformatic pipelines optimized for the purpose.

Four reasons for choosing SeqOne to power your lab

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

Support: 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.

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.

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

Let SeqOne boost your lab’s performance !