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Join a panel webinar featuring five PhD experts discussing the critical challenge of standardizing somatic variant interpretation in next-generation sequencing (NGS) oncology panels. Explore how the increasing use of NGS in precision oncology has created industry-wide variability in variant interpretation across laboratories, leading to confusion for clinicians and patients who rely on genetic information for healthcare decisions. Learn about the issues surrounding standardization of variant interpretation as experts examine how interpretation guidelines and clinical decision support software can help reduce variability between laboratories. Discover the impact of inconsistent variant interpretation on patient treatment decisions and clinical trial enrollment in hospital and academic settings. Participate in live Q&A sessions with leading specialists in NGS testing and clinical informatics who provide insights into current challenges and potential solutions for improving the reliability and consistency of genomic data interpretation in precision medicine.
