Your strategy calls for an outsourcing of NGS data interpretation? Not a 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 for optimal complementarity of 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.

If independence is key and you chose to generate your own reports, omnomicsNGS will speed up your interpretation remarkably 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, independently of DNA capture kit, omnomicsNGS will help make bioinformatics user-friendly. Start interpretation from your variant calling (.vcf) file, 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 a larger IT infrastructure.

Genomic analysis as 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 IT infrastructures.

Deep integration is about so much more than valid reports. It is about data standards, exchange, consistency, and quite importantly about updating reports automatically, 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.