Two Clinical Workflows

From Unfiltered Variants to a Clinical Report

About this webinar

Recorded On: Wednesday, November 4, 2015

Clinical labs need to be able to process samples down to a shortlist of variants and publish a professional report. Two common clinical applications for genetic tests include Cancer Gene Panels and Whole Exome Trios. Using VarSeq and VSReports, we will demonstrate how easy it is to go from a variant file created by a secondary analysis pipeline containing unfiltered variants to a report containing information for variants of interest. Along the way, we will discuss tips and tricks and answer frequently asked questions to help you get the most out of your data!

This webcast will present a thorough overview of VarSeq's support for clinics:

Cancer Gene Panel

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

Whole Exome Trio

  • Variant Quality Assurance
  • Filtering to variants matching several inheritance patterns
  • Summarizing variants in a clinical report

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