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
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