Activity
Mon
Wed
Fri
Sun
Aug
Sep
Oct
Nov
Dec
Jan
Feb
Mar
Apr
May
Jun
What is this?
Less
More

Owned by Lutfiya

AH
AI & Health Science

1 member โ€ข Free

Memberships

AI Marketing Hub, SEO & Search

4.3k members โ€ข Free

AI Marketing Hub Pro

218 members โ€ข $88/m

AI Automation Society

415.6k members โ€ข Free

Early AI-dopters

1.3k members โ€ข $77/month

AI Automation Vault

18.4k members โ€ข Free

Trillet AI

367 members โ€ข Free

AI Bits and Pieces

797 members โ€ข Free

BioAutomators

113 members โ€ข Free

7 contributions to BioAutomators
Apr 30 โ€ขย 
General discussion
๐Ÿšจ ALL 10 CHAPTERS + APPENDIX ARE LIVE IN THE CLASSROOM.
Chapters 6 through 10 just dropped โ€” plus Appendix A for anyone who needed a Git/GitHub walkthrough before deploying. This is the final batch. PGx Guardian is complete. What you now have: ๐Ÿงฌ A genotype agent that reads real VCF files ๐Ÿ”— A DGI agent matching genes to CPIC clinical guidelines โš ๏ธ A DDI agent checking every drug pair for dangerous interactions ๐Ÿ“‹ A report agent writing clinical + patient summaries via Gemini 2.0 Flash ๐ŸŽ™๏ธ A voice interface for hands-free clinical workflows ๐Ÿš€ A deployed app with a real public URL Every step has a test command so you know it works before moving on. Go finish it. The classroom is waiting. ๐Ÿงฌ Drop any questions in the comments - that's what we're here for.
0 likes โ€ข Apr 30
@Dr. L Thanks for sharing! ๐Ÿ‘๐Ÿผ
Dec '25 โ€ขย 
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. ๐Ÿ‘‰ Go to Course Room โ†’ Variants Annotation Workflows โ†’ Download Template Questions? Drop them below.
0 likes โ€ข Feb 14
@Dr. L Thank you so much for sharing! This is really cool, Iโ€™m excited to dig in! Thank you again ๐Ÿ™๐Ÿผ
Feb 13 โ€ขย 
General discussion
New in Classroom: TalkToOpenTargets AI Agent
Just added a new lesson to the Discovery Engine course showing how to build an AI agent that queries the Open Targets Platform using natural language. What you'll learn: - Setting up an n8n AI agent with GraphQL tools - Querying gene-disease associations conversationally - Integrating Open Targets + PubMed in one workflow - Handling complex multi-step research questions 2-minute demo video shows the agent finding top Parkinson's genes, checking drug status, retrieving pathways, and pulling recent research papers - all from natural language questions. Includes: - Complete n8n workflow template (import-ready) - System prompt with Open Targets GraphQL schema - Setup guide + troubleshooting Check it out in Classroom โ†’ Discovery Engine โ†’ TalkToOpenTargets lesson. Questions? Drop them below
0 likes โ€ข Feb 14
Thank you ๐Ÿ˜Š
Dec '25 โ€ขย 
General discussion
Stop Chasing Papers โ€” Let Them Come to You
๐Ÿ””๐Ÿ”” NOTE: the session on 23/12/2025 is fully booked, please sign in to the next one in January.๐Ÿ””๐Ÿ”” 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 โ€” 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 โ€” new publications - bioRxiv โ€” preprints - ClinicalTrials.gov โ€” recruiting trials - Google Patents โ€” IP filings - Europe PMC โ€” open access papers All free APIs. No coding required. Just bring your laptop and your favorite gene. ๐Ÿ“… Date: [23/12/2025 & 20/01/2026] โฐ Time: [20:00 CET] register here --> LINK
1 like โ€ข Dec '25
@Dr. L Thanks for hosting this. Just signed up, looking forward to it! ๐Ÿ˜Š
Nov '25 โ€ขย 
General discussion
๐Ÿš€ Launching the TalkToClinVar Course Series! ๐ŸŽ‰
Hello BioAutomators! ๐ŸŽ‰ The TalkToClinVar course is officially launching, and the excitement is sky-high. This six-video series takes you from the very first setup steps all the way to a fully working agent that loads ClinVar into Azure PostgreSQL, connects it to n8n, and transforms everything into an automated variant-querying powerhouse. Each episode is practical, clear, and built to give you that satisfying โ€œit finally works!โ€ moment. If anything acts up along the way, just drop a comment and Iโ€™ll help you get unstuck. ๐Ÿš€ P.s: Youโ€™ll find the full course inside the Classroom tab.
0 likes โ€ข Nov '25
@Dr. L Wow, this sounds so powerful, and am excited to jump in! Thank you again!
1-7 of 7
Lutfiya Miller
1
1point to level up
@lutfiya-miller-9048
Toxicologist by day, DJ by night. Exploring coding, AI, and large language models. Always learning, always creating. ๐Ÿ”ฅ๐ŸŽง๐Ÿ’ป

Online now
Joined Nov 22, 2025
INFJ