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The omnomicsNGS variant interpretation and reporting platform provides both independent clinicians and molecular genetics laboratories with the tools to find and analyse genomic and variant information based on patient data, local knowledge and a large bank of external trusted data sources. Generate clear reports quickly and easily, and find all of your variant interpretation needs in one place.

  • Quickly generate genetic or oncology reports according to ACMG/AMP/ASCO/CAP guidelines.
  • Simplify variant classification through automation or dig deep for SNV, InDel, CNV, SV in rare genetic disorders using NGS panels, whole exomes or genomes
  • Make coverage analysis and QC an integral part of the reporting process
  • Easily integrate into your existing pipelines and IT infrastructures for clinical oncology or other genetic testing
  • Keep your data private – install locally or use on the cloud
  • Collaborate and exchange data for clinical research projects, or together with a biobank as a repository for genomic variants.

omnomicsNGS is CE-marked medical device class I for medical use in Europe.

Key benefits:

Customisable Reports
Centralised Data
Pipeline Integration
Customisable Reports

Genetics Analysis Report

Does your strategy call for an outsourcing of NGS data interpretation? Not an NGS variant interpretation specialist? No problem. Help is available. You have the sample or the sequence of the sample. We can take care of the rest and deliver laboratory reports for specified genes or based on the requirements of the case.

Partner with us to complement your in-house expertise or get started with a few samples. We use omnomicsNGS to help you provide fast and comprehensive services. When you are ready to expand your services and perform interpretation and reporting independently, the omnomicsNGS data can be transferred.

Centralised Data

For independent variant interpretation

If independence is key and you want to generate your own reports, omnomicsNGS will speed up your interpretation and improve your efficiency by providing automation for gene panels and great flexibility for more complex analyses. A systematic approach ensures accurate diagnoses, appropriate care, and patient safety.

With data from your own NGS sequencer or from a partner, regardless of DNA capture kit, omnomicsNGS will help make bioinformatics user-friendly. Start interpretation from your variant calling (.vcf) file, where support is available for optimising your variant calling process. Create virtual gene panels, biomarkers, filters, and integrate your domain expertise. Gather clinical evidence and classify variants according to ACMG guidelines. For somatic tests, ASCO 4-tier reporting is also available. omnomicsNGS offers seamless integration into larger IT infrastructures.

Pipeline Integration

Genomic analysis as an integral part of a large health provider organisation

Genomic data is never interpreted in isolation. How are you integrating patient records or clinical research with clinical diagnostics development? Hospital, university, drug development – all can benefit from different pieces of the same knowledge base. omnomicsNGS has been designed to be easily integrated into large, complex IT infrastructures.

Deep integration is about so much more than valid reports. It is about data standards, exchange, consistency, and staying up to date, as new facts and observations emerge in the field of biomedical research.

From laboratory bench to bed side, think big enough, so you can do it right each time, every time.

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