Tackling Complexity in Oncology Biomarker Interpretation with CGW Plus
Watch ow for a discussion of challenges and innovative solutions in clinical genomics workflows. Discover how laboratories leverage variant databases and medical genomics knowledge to automate and accelerate the analysis and reporting of genomic alterations in oncology. We also introduce Velsera’s completely reimagined solution to these challenges, CGW Plus, showcasing its variant quality assessment, clinical evidence review, and adaptive learning and memory capabilities.
What you will learn in this webinar:
- How laboratories are leveraging variant databases and medical genomics knowledge to streamline workflows.
- The advanced capabilities of CGW Plus, including variant quality assessment, clinical evidence review, and adaptive learning and memory features.
- Practical solutions to overcome the bottlenecks in oncology variant analysis and enhance the efficiency and accuracy of your laboratory operations.
Meet the speaker:
Jason is a Director of Product Management at Velsera, where he leads the product team responsible for the Clinical Genomics Workspace (CGW) platform. He has held multiple key software product development roles at Velsera since joining in 2019. With over 10 years of experience in molecular diagnostics, Jason has focused on creating clinical Next-generation sequencing (NGS) software and solutions for oncology and genetic disease testing.