Automating Clinical Workflows with the VarSeq Suite

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About this webinar

March 16, 2022

Presented By: Dr. Nate Fortier, Director of Research

The automation of clinical NGS workflows provides a number of important benefits. Automation reduces the time required to produce a clinical report, mitigates the possibility of human error, and improves the precision of clinical results. In this webcast, we will discuss how the VarSeq Suite can be leveraged to automate the full analysis workflow from sequencer to clinical report. Join us as we demonstrate how VarSeq’s automation capabilities can enable your laboratory to:  

  • Automatically perform secondary analysis when a new sequence run is complete
  • Go from FASTQ to BAM and high-quality variants in VCFs using Sentieon
  • Automatically start VSPipeline to go from raw VCFs to candidate variants
  • Compute coverage and call CNVs alongside small variants with VS-CNV
  • Efficiently interpret a small set of annotated candidate variants and CNVs
  • Draft reports with VarSeq and VSClinical

    • Join us as we discuss the automation of the clinical analysis process for NGS genetic tests from FASTQ to Clinical Reports using the VarSeq Suite and discover how your laboratory’s NGS workflows may benefit from these automation capabilities.  

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