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.

Dale Watkins

Analyzing Complex Genomic Variants in Somatic Cancer


Previous registration necessary?


Simultaneous translation ?


Will it be recorded?


Amber Leigh


Link to the Event

Banner to the Event

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

Download the Agenda

Search for our next event. See you soon!

Subscribe to get news on all upcoming events


Social Media

  • Twitter DocMeetings
  • Instagram DocMeetings
  • Facebook ícone social
  • LinkedIn ícone social

contact us


Sao Paulo, SP - Brazil

© 2020 by Docmeetings - A Company
Site Managed by:
QUALITY Soluções Web
1996-2021 "25 years inspiring technology"