kemal
5463f489a3
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End-to-end variant interpretation platform for rare genetic disease research: SvelteKit UI, FastAPI + PostgreSQL API, Nextflow/Ensembl VEP pipeline, LightGBM pathogenicity scoring with MLflow, K8s/ArgoCD/GCP infrastructure. Public test data only; no clinical claims.
5 lines
119 B
JSON
5 lines
119 B
JSON
{
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"extends": "./.svelte-kit/tsconfig.json",
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"compilerOptions": { "strict": true, "moduleResolution": "bundler" }
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}
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