About this webinar

Recorded On: Wednesday, March 3, 2016

Clinical labs must have the ability to go from a collection of samples and associated variants to a professional report documenting a shortlist of clinically relevant variants. Cancer Gene Panels are a common clinical application for genetic tests. In this webcast, we will show VarSeq and VSReports can be used to go from an unfiltered variant file created by a secondary analysis pipeline to a report containing information about interesting variants. 

This webcast highlights VarSeq's support for Cancer Gene Panels and Tumor-Normal workflows by demonstrating: 
 

• Variant, Region and Sample Quality Assurance 
• Filtering to variants in targeted cancer genes relevant to the tumor type 
• Summarizing variants in a clinical report