Next-Gen Sequencing Workshop: How to Effectively Derive Meaning from DNA Variant Data

Learn more about Golden Helix’s SNP & Variation Suite (SVS) – a powerful and integrated collection of high-performance analytic tools for managing, analyzing, and visualizing large-scale sequence and array-based data. Applications of SVS include candidate gene analysis, genome-wide association, copy number analysis, and next-generation sequencing. This webinar will focus primarily on rare variant analysis for DNA-sequencing.

The presentation will cover the following:

• Introduction to SVS
• Managing variant data and genomic annotations
• Filtering and classification workflows to identify variants likely to be damaging
• Visualizing SNVs and indels in a genome browser to compare variant pattern differences between sample groups
• Assessing rare variant burden using collapsing and association methods