Date
From:
To:
Lieu / Hôte

Virtual Event

A major challenge in the era of precision medicine is to ensure quick and reliable identification of potentially disease-causing genetic variants with a streamlined workflow.  

This webinar will focus on how SOPHiA overcomes these challenges by enabling experts to deal with the vast amounts of genetic data coming from both targeted and exome applications, and how to accurately detect the variants of interest. You will have the opportunity to discover how our platform offers advanced analytical performance in calling challenging variants like large Indels, CNVs, Alu insertions, and Boland inversions. Additionally, you will learn how SOPHiA manages difficult research contexts such as pseudogenes or homopolymeric regions.   

This session is a must-see for laboratories using Next-Generation Sequencing for hereditary disorders, willing to implement an efficient and reliable secondary analysis solution in their routine workflow. 

Research Use Only (RUO), Not for Use in Diagnostic Procedures 
The information included has been prepared for and is intended for viewing by a global audience. Information about products which may or may not be available in different countries and if applicable, may or may not have received approval or market clearance by a governmental regulatory body for different indications for use. Please consult local sales representatives.

Agenda
5:00pm (CET) / 11am (EST) : Advanced germline variant analysis with the SOPHiA Platform
5:50pm (CET) / 11:50am (EST) : Q&A
6:00pm (CET) / 12:00pm (EST) : Closing

i-news-events