Asia Pacific Region Webinar: Analyzing Complex Genomic Variants in Somatic Cancer

8/6/20, 11:30 AM
Asia/New Dheli +5:30

Description

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.

Previous registration necessary?

NO

YES
Simultaneous translation ?

NO

YES
Will it be recorded?
NO
YES

Dale Watkins

Analyzing Complex Genomic Variants in Somatic Cancer

Inglês

 

Speakers

Amber Leigh

 

Link to the Event

Banner to the Event

Asia Pacific Region Webinar: Analyzing Complex Genomic Variants in Somatic Cancer