I built an open-source dashboard for analyzing whole genome sequencing data using Google DeepMind's AlphaGenome API.

After getting my WGS data from Dante Labs a few years ago, I wanted a better way to explore my variants beyond the basic reports they provide. When DeepMind released the AlphaGenome API, I saw an opportunity to build something more powerful.

The main limitation right now is that raw VCF files from consumer WGS services often lack gene annotations (VEP/SnpEff). The dashboard works best with annotated VCFs, but I've added rsID-based lookups as a fallback.

Would love feedback, especially from others who've been exploring their own genomic data.