Flexible for you, from filtering strategies and virtual gene panels, to compatibility with any sequencer and kit. Whatever the clinical domain, omnomicsNGS puts the power in your hands.
Generate genetic or oncology reports according to ACMG/AMP/ASCO/CAP guidelines. CE-IVD marked under IVDD (98/79/CE).
Coverage analysis and other clinical QC metrics included automatically to reports. Define your own threshold values most important quality metrics.
All clinical domains
From clinical oncology to rare diseases diagnostics, OmnomicsNGS streamlines and automates any clinical domain the lab expands into.
Safe and secure
Can be used from the cloud or installed on your premises behind the firewalls to keep confidential patient data safe and secured.
The tools are in your hands
With access to over 150 filterable metrics and integration of large amounts of data, you have everything you need in one place to get the most out of your data.
Flexible for you
Edit your filtering rules, report templates, virtual gene panels and much more from within the software. omnomicsNGS works for you and your needs.
Used by clinicians around the world
From oncology to germline testing, and carrier screening to inherited diseases.
omnomicsNGS is used by both public and private laboratories to run their clinical diagnostics.
Dr Kanya Suphapeetiporn
Professor of Paediatrics and Head of Division of Medical Genetics and Metabolism
The key for us in deciding which software to choose as we develop our testing capacity was the user-friendliness. omnomicsNGS is very easy to use, giving us all the information we need and with really strong filtering techniques. We are confident that as we scale our operations, omnomicsNGS will continue to be the tool for us.
Molecular Pathology Laboratory Supervisor
Euformatics has been instrumental in implementing NGS testing with us – the support and guidance that they are providing is really valuable. I am sure that omnomicsNGS and omnomicsQ will be a part of our NGS pipeline for a long while to come.
Our laboratory has high sequence data production capacity and many pipelines and kits in use, but omnomicsNGS helps us to get through samples in a systematic and reproducible way. As we are the largest biopsy and cytology lab in the Czech Republic, omnomicsNGS let us save valuable time.
Our focus is on preventative medicine and identifying predispositions to chronic diseases by analyzing both common and rare variants. At Archetope we have used OmnomicsNGS as core tool to interpret, annotate, classify and report genetic variants in a clinical environment. It has allowed us to optimize our workflows and improve our skills in understanding human genetics from a clinical perspective.
omnomicsNGS is built with flexibility as its core, to help you get the most from your NGS data
omnomicsNGS is designed to easily integrate into whatever pipeline you already have, including electronic patient record systems, LIMS and more. Let omnomicsNGS become a seamless part of your operations.