Congenica Oncology

The time has come to change the way we treat cancer

Over a quarter of all individuals diagnosed with advanced cancer are now eligible for a treatment based on the genomic analysis of their tumour, driven by the ever-increasing availability of biomarkers and associated treatments.

However, integrating molecular tumour profiling into routine clinical care remains challenging, and the diagnostic journey for laboratories, patients and their treating clinicians is still complicated, expensive and slow.

Analysis and interpretation of the often large and complex data sets has been identified as the biggest bottleneck, together with the inability to provide accurate and relevant therapy recommendations in user-friendly reports that enable rapid patient treatment.

Transforming Cancer Care

Watch our Satellite Symposium from ESHG 2023 to hear:

Andrew Biankin talking about his experience in transforming cancer care by use of genomic testing
Philip Beer discussing new approaches to automate somatic driver annotation for evidence-based variant interpretation and increased patient sample throughput
Gavin Xu introducing Congenica’s novel Precision Oncology solution.

Automation is key to accelerate the diagnostic journey and drive Precision Oncology

At Congenica we have developed a fully automated CE-IVD approved Precision Oncology platform for rapid and unbiased interpretation of next generation sequencing data without the need for manual intervention. This not only reduces reporting times from hours to minutes, but eliminates the need for difficult-to-hire expert staff and paves the way for cost-effective routine cancer care.

Transforming Cancer Care

To find out more about our Precision Oncology Platform, please view our brochure.

From data to report without manual intervention

Our future-proof end-to-end solution consists of fully automated and integrated secondary and teritary analysis pipelines coupled with automated, user-friendly reporting that is focused on actionable insights to support rapid treatment decisions. Automated treatment matching is powered by NCCN, ESMO, NICE and SMC best practice guidelines with authorised therapeutic assertations from the FDA, EMA and MHRA.