Move from a raw VCF to prioritized candidates through annotation, evidence-based filtering, and practical variant-interpretation workflows.

Once variants have been called, the challenge is finding the candidates that deserve closer investigation. This course shows you how to enrich a VCF with annotations, filter variants systematically, and use evidence and prioritization tools to focus your analysis.
Part 2 of the WES pathway uses practical examples from five patient datasets. Excel and Linux command-line methods are taught alongside automated tools so you can understand how data, filters, and interpretation connect.
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Experienced instructor in bioinformatics and computational biology.