Decoding Breast Cancer Genomics: Navigating NGS Data

This webinar focuses on breast cancer genomics and explains how NGS data is generated, analyzed, and interpreted in research and clinical settings. Participants will gain a clear understanding of how genomic variations drive breast cancer development and progression. The session introduces key NGS approaches used in oncology, including targeted sequencing and panel-based testing. Learners will explore the difference between germline and somatic variants and their clinical relevance. Real-world case studies help translate complex genomic data into meaningful biological insights. The webinar bridges genomics research with precision oncology applications. It is ideal for learners interested in cancer bioinformatics and translational genomics.