Automate, Import, & Interpret: Using Custom Scripts in VSClinical

As genomic data grows in complexity, flexible and automated NGS analysis workflows are more essential than ever. While VarSeq offers a robust, user-friendly platform for variant analysis and clinical reporting, many users work in environments that require tailored solutions. This webcast explores VarSeq’s deployment and customization capabilities, empowering users to extend their pipelines with automation and custom evaluation scripts. From desktop installations to cloud-hosted Warehouse Workspaces, we’ll demonstrate how users can automate processes like variant import, custom data import, variant evaluation, and reporting. Real-world examples will showcase how custom scripting streamlines complex tasks, saves time, and adapts to diverse clinical needs.
Viewers will learn: