YOUR GENOMIC ANALYSIS PROCESS SeqOne provides you with an integrated system that manages your genomics analysis process from raw data to final results.
SeqOne is designed from the ground up to improve your efficiency and accuracy in analysing genomic information at scale. Our platform automates many tasks that today cost you time and introduce the risk of errors. You will find that you can perform more analyses and obtain more detailed insights from every analysis.
SeqOne is open. We believe that the open-source community is the best way to provide cutting-edge bioinformatic pipelines with proven performance and robust, reliable behavior. Our platform incorporates pipelines that have been benchmarked to ensure optimal performance.
Fast responsive filtering to find causal variants
An easy-to-use, visual environment
Choose your analysis at the click of the mouse
View in-depth quality reports
SeqOne's platform includes bioinformatic applications optimised to provide medically actionable results in the following areas
SeqOne’s mission: to make genomic medicine accessible to everyone
Next Generation Sequencing (NGS) has made obtaining detailed genomic information more affordable than ever. Yet today, the challenge is to find ways to cost-effectively analyse all this raw genomic data while ensuring quality of the results. SeqOne’s mission is to provide advanced genomic analysis tools that make it possible to analyse NGS data cost-effectively at scale and hence to ensure that the benefits of genomic medicine are available to everyone.
Are you a guru in bioinformatics, molecular biology, machine learning or high-performance big data infrastructure? Do you want to change the way in which the healthcare industry meets its challenges?
SeqOne is an open platform that lets users easily access and use the best genomics analysis software without needing advanced computer skills. If you have developed an open-source bioinformatic pipeline and are looking for a way to reach a larger user base, SeqOne can help.
The SeqOne bioinformatic developer programme provides the support and resources to help you make your pipeline easier to use and accessible to many more potential users.
Challenges and importance of mid-sized deletion identification for genomic medicine
The clinical importance of mid-sized deletions is becoming increasingly apparent with a growing number of variants of this type being identified as pathogenic in the literature. These deletion variants are challenging to identify using traditional pipelines which struggle to align them. This document describes a new approach developed by SeqOne that facilitates the identification of […]Read more See all