A New AI-Powered Tool for Human Gene Research – Your Feedback Matters!

Dear colleagues,

I'm excited to share a research-focused AI tool I developed to support the genomics and biomedical research community: HG-database – a specialized assistant for exploring human genes, variants, and genomic datasets.

This tool was custom-built by me, not just as a general chatbot, but as a smart companion for gene-level research. It’s based on GPT architecture but fine-tuned for human genetics and bioinformatics.

🔍 What HG-database offers:

• Accurate interpretation of HGVS variant nomenclature
• Integration with databases like GeneCards, Ensembl, GTEx, UniProt, ClinVar, OMIM, HGMD
• Functional annotation via Mutalyzer and Ensembl VEP
• Cross-referencing genes with diseases, phenotypes, expression patterns, and regulatory elements
• Direct support for SNPs, CNVs, and transcript-level data

🧬 What makes it different from ChatGPT?

• HG-database is research-focused: built for gene scientists, not for general conversation
• Links directly to genomic databases with embedded references
• Understands gene symbols, aliases, chromosomal locations, and variant impacts at the transcript level
• No hallucinations: all outputs are based on validated bioinformatics resources

📢 Why I need your feedback:As a genetics researcher, I built this tool to fill a gap I personally experienced. Now, I’d love your insight:

• What works well?
• What should be improved?
• What new features would help your research?

This assistant is not a diagnostic tool—it's designed purely for education, annotation, and exploration in human genetics.

🧪 Ready to try it out? I’d be happy to guide you or send a walkthrough.

Thank you in advance for your input—it means a lot to help improve this tool for our scientific community.

📬 Feel free to message me directly or comment with your impressions.

URL: https://chatgpt.com/g/g-67ebfcf8b158819199fb846135b3c651-hg-database