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. |
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