Next-Gen Sequencing at Scale: Transforming Per-Sample Variant Outcomes into Institutional Knowledge with VSWarehouse

As Next-Generation Sequencing (NGS) becomes a cornerstone of clinical diagnostics and research, laboratories are seeking solutions that not only streamline per-sample variant interpretation but also leverage the collective genomic intelligence gained across all analyses. In this webcast, we explore how VSWarehouse connects single-sample precision with cross-sample insight—transforming routine variant analysis into a scalable, knowledge-driven process.

Attendees will see how VSWarehouse enables detailed per-sample variant interpretation following AMP and ACMG guidelines, while simultaneously capturing and centralizing these findings to build a cohort-wide variant knowledge base. From reusing variant classifications to annotating internal allele frequencies, VSWarehouse provides powerful capabilities to optimize variant analysis, accelerate turnaround times, and elevate genomic understanding across your organization.