Introducing the most advanced platform for clinical genomic analysis…
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
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.
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
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.
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.
6 May 2022
SeqOne posters at the ESHG; using ML and big data to improve variant interpretation
SeqOne will be at the ESHG show in Vienna in hall X4 booth 664. We will be presenting four posters hi lighting various projects by [...]
4 February 2022
SeqOne Genomics – partenaire industriel du consortium FrOG (French OncoGenetics)￼
Pour le développement de FrOG, une base de données nationale centralisée et partagée, destinée à améliorer la prise en charge des patients en oncogénétique Paris, [...]
4 February 2022
SeqOne Genomics selected as genomic analysis solution for CELIA (Comprehensive Genomic profiling impact) project, in collaboration with Illumina
The project aims to compare the clinical utility of broad-spectrum genomic profiling in the treatment of late-stage cancer patients with more traditional approaches that analyze [...]
4 February 2022
SeqOne Genomics annonce son implication dans le projet « Célia » (Comprehensive Genomic profiling impact) aux côtés d’Illumina
• Ce projet vise à évaluer l’utilité clinique du profilage génomique complet (CGP) dans la prise en charge thérapeutique de patients atteints d’un cancer à [...]