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
Introducing the most advanced platform for clinical genomic analysis…
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.
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.
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.
CHU Montpellier, France
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.
2 February 2024
Evaluating Pathogenicity Scoring system for Missense Variants on real-world data: A comparison between AlphaMissense and SeqOne DiagAI pathogenicity score
Context Predicting the impact of missense mutations remains a significant and complex challenge in human genetics. Approximately 98% of these amino acid substitutions are classified [...]
30 January 2024
SeqOne Genomics appoints Martin Dubuc as Chief Executive Officer
SeqOne Genomics, an award-winning French HealthTech startup specializing in AI-powered clinical genomics, is pleased to announce the appointment of Martin Dubuc as its new Chief [...]
26 October 2023
SeqOne Genomics appoints Martin Dubuc, Senior Pharmaceutical and Digital Health Executive to its Board of Directors
M. Dubuc will strengthen the Board’s capabilities in the fields of personalized medicine and companion diagnostics Montpellier, France - Thursday, 26th of October, 2024 – [...]
12 October 2023
Seamlessly transition from Agilent Alissa Interpret genomic data analysis software to SeqOne Platform
Discover SeqOne, the ultimate interpretation solution and Alissa Interpret alternative, compatible with Agilent wetlab! Talk to our experts Agilent’s genomic data interpretation software, Alissa Interpret, [...]