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.

I’ve uploaded a template that checks several publication sources, filters them by genes and diseases (that you can specify), summarizes them with AI, and sends a digest by email. This is useful if you want to keep track of new papers without checking platforms manually. You can adjust the schedule, search parameters, time window, and email delivery. The template and setup steps are posted here. If anyone adapts or improves it for other research use cases, feel free to share.

🔔🔔 NOTE: the session on 23/12/2025 is fully booked, please sign in to the next one in January.🔔🔔 FREE ONLINE WORKSHOP ANNOUNCEMENT One workflow replaced 5 daily searches I used to do manually. I got tired of checking PubMed, then bioRxiv, then ClinicalTrials.gov, then Google Patents... you know the drill. Always behind, always missing things. So I built a single n8n workflow that: - Queries all 5 databases on a schedule - Filters by my specific genes, diseases, and competitor names - Uses AI to summarize what's actually worth reading - Sends me one clean daily or weekly digest Now I catch preprints before they're published, see clinical trials the day they open, and know when competitors file patents — without opening a single website. And I want to show you exactly how to build it. Join me online for a free hands-on workshop! We'll build the full workflow together, step by step. By the end you'll have a working system that monitors: - PubMed — new publications - bioRxiv — preprints - ClinicalTrials.gov — recruiting trials - Google Patents — IP filings - Europe PMC — open access papers All free APIs. No coding required. Just bring your laptop and your favorite gene. 📅 Date: [23/12/2025 & 20/01/2026] ⏰ Time: [20:00 CET] register here --> LINK

This is where it gets wild ! You're about to watch me build an AI agent that talks to ClinVar like it's your research partner. No joke. Type a question in plain English → AI converts it to SQL → executes against 2.5M variants → returns answers in seconds. We're wiring n8n to Azure PostgreSQL, teaching the AI agent to understand genomics questions, and building the entire conversational interface from scratch. By the end of this video, you'll have ClinVar responding to you like a colleague who never sleeps. This is agentic AI doing actual science. Watch Step 3 now:here Who's building this with me? 🚀

Hey Bioautomators! I just added a brand new tutorial to the TalkToClinVar Course Series! 🚀 “How to Set Up DBeaver to Import ClinVar Data to Azure PostgreSQL” This step-by-step lesson covers: ✅ Connecting DBeaver to Azure PostgreSQL ✅ Importing ClinVar genomic variant data ✅ Handling data mapping and transformations ✅ Troubleshooting common issues This is a crucial step in building your ClinVar automation workflow! 💡 🔗 Check out the new lesson in the course now! Work through it at your own pace, and if you have any questions or run into any issues, drop them in the comments below. I’m here to help! 👇 Let’s keep building together! 🔬💻