Increasing case throughput: How to gain immediate insight into clinically relevant evidence
In this webinar we look at a key part of the clinical interpretation workflow and reveal how a combination of new tools is helping to break through the interpretation bottleneck, enabling you to instantly identify and analyze genetic evidence found across the complete corpus of scientific articles, faster and with greater confidence than ever before.
Watch the webinar to discover:
- How to gain immediate insight into evidence relevant to your cases from over 7.5 million published articles
- How to prioritize your search results by clinical relevance and find what you are looking for 10-times faster
- How to maximize your workflow efficiency to reduce costs, increase case throughput and provide better patient outcomes
Helen Savage, DipRCPath
Deputy Head of Clinical Services, Congenica
Helen is a Clinical Scientist with 12 years' experience working in the NHS and biotech industry. She is skilled in variant interpretation across rare disease and cancer, feeding her clinical experience into Product Management in Congenica, to develop a best-in-class software solution for the analysis and interpretation of genetic data for patients with rare disease.
Mark Kiel, MD, PhD
Co-Founder and CSO, Genomenon
Mark oversees Genomenon’s scientific direction and product development. After spending 15 years preparing for a life of academic research, Mark became convinced that revolutionary change in genomics was more likely to emerge out of industry. In 2014, he founded Genomenon – a life science IT company addressing the challenge of connecting doctors with evidence in the literature to help diagnose patients with genetic diseases and cancer.