Genomic researchers waste time wrestling with clunky tools to explore DNA variant databases.
Develop a web-based visualizer with intuitive filtering—by population frequency, pathogenicity scores, or genomic region. Plug into existing APIs like AlphaGenome.
Universities and pharma companies would pay for team licenses. Offer a free tier for academic use.
Launch with one focused visualization (like variant clustering) before expanding.
The risk is slow adoption if tools don’t integrate with lab workflows.