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Explore wet laboratory workflows and design considerations essential for implementing next-generation sequencing (NGS) diagnostics in oncology through this 57-minute webinar presented by Dr. Jeremy Segal, MD, PhD, Assistant Professor of Pathology and Director of Molecular and Cytogenetic Pathology. Learn to recognize how sample quality and quantity directly impact NGS data quality while understanding the fundamental creation and purpose of DNA libraries. Compare amplicon versus hybrid capture sequencing chemistries and identify key considerations for designing effective hybrid capture oncology panels. Examine specimen types, specimen management protocols, extraction methods, quantification techniques, and various library preparation approaches for DNA analysis. Discover basic methods for fusion detection using RNA and identify major workflow pitfalls that can affect data quality and reliability in clinical oncology diagnostics. Gain practical insights into specimen management best practices and technical considerations that ensure accurate and reliable NGS results in pathology laboratories. Earn PACE credits by completing the webinar and accessing the certification through Labroots' platform, with credits valid until January 29, 2027.
