Asia Pacific Region Webinar: Analyzing Complex Genomic Variants in Somatic Cancer
Asia/New Dheli +5:30
Next generation sequencing (NGS) technologies facilitate the accurate detection of genetic variants. Yet, the process of analyzing and classifying more complex alterations using a standard variant lookup table remains challenging.
In this informative webinar, done specifically for the Asia Pacific region, we focus on gene fusions, co-occurring variants, copy number variants, and tumor mutational burden (TMB), and we provide practical strategies for analyzing and classifying these complex variants using a highly-curated, rules-based knowledgebase in the context of somatic cancer.
By attending this webinar, you will:
Gain strategies for filtering, classifying, and interpreting variants within a clinical context.
Learn about bioinformatic methods for calling variants and assessing quality.
See example reports using de-identified samples for several popular NGS assays, including Archer VariantPlex® and FusionPlex®, TruSight™ Oncology 500, and AmpliSeq.
Analyzing Complex Genomic Variants in Somatic Cancer
Previous registration necessary?
Simultaneous translation ?
Will it be recorded?