From Panels to Genomes with VarSeq: The Complete Tertiary Platform for Short and Long-Read NGS Data

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About this webinar

January 17th, 2024 // 12:00 PM EST

Presented By: Jennifer Dankoff, Ph.D., Field Application Scientist

From gene panels to whole genome, from short to long-read sequencing, the VarSeq suite is the solution for NGS analysis and reporting in a modern clinical lab. VarSeq handles the spectrum of variant types (SNV, Indel, CNV, Fusions) and provides automated classification and reporting capabilities following the ACMG and AMP guidelines. With our new PacBio partnership, we are more adaptable than ever with creating a spectrum of custom workflows to suit our unique user needs.

This webcast will review:

  • Data analysis scaling from Gene Panel to Genome analysis with VarSeq and VSWarehouse.
  • Analysis and annotation of SNVs, Indels, CNVs, and fusions.
  • A close look at a PacBio long-read trio analysis.

  • Watch us for this showcase in modern VarSeq analysis capabilities.

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