Dec '25 • General discussion
Variants Annotation Across 5 Databases
The template you've been asking for is finally here.
Head to the Classroom right now and grab the Variants Annotation Workflow.
What it does: Drop your genetic variants into a Google Sheet. The n8n workflow automatically queries:
- ClinVar (pathogenicity)
- PubMed (research papers)
- dbSNP (variant IDs)
- UniProt (protein function)
- gnomAD (population frequency)
Everything comes back annotated. Ready to analyze.
This is for you if:
- You've downloaded your 23andMe/MyHeritage raw data and have no idea what it means
- You're a researcher tired of manual database queries
- You want to see bioautomation in action
Demo video included so you can see exactly how it works before you set it up.
No bioinformatics background needed. Just import the template and follow the setup guide.
👉 Go to Course Room → Variants Annotation Workflows → Download Template
Questions? Drop them below.
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Variants Annotation Across 5 Databases
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