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

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.

Dale Watkins

Analyzing Complex Genomic Variants in Somatic Cancer

Inglês

Previous registration necessary?

NO

YES
Simultaneous translation ?

NO

YES
Will it be recorded?
NO
YES
 

Speakers

Amber Leigh

 

Link to the Event

Banner to the Event

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

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