w Cancer Workflows in VarSeq

Cancer Workflows in VarSeq

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 

Watch on demand

Please enjoy this webcast recording. Should you have any questions about the content covered, please reach out to our team here.

Download the slides

To download a copy of the slides, click on the LinkedIn icon. This will redirect you to the SlideShare site. From there, you can clip your favorite slides or download the entire deck to your computer.

Love this webcast? Check out more!

Find out how Golden Helix software enables users to harness the full potential of genomics to identify the cause of disease, improve the efficacy and safety of drugs, develop genomic diagnostics, and advance the quest for personalized medicine.

Webcast Library