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.
24 lines
563 B
JSON
24 lines
563 B
JSON
{
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"name": "rarelens-web",
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"version": "0.1.0",
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"private": true,
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"type": "module",
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"scripts": {
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"dev": "vite dev",
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"build": "vite build",
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"preview": "vite preview",
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"check": "svelte-kit sync && svelte-check --tsconfig ./tsconfig.json",
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"test": "vitest run"
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},
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"devDependencies": {
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"@sveltejs/adapter-node": "^5.2.0",
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"@sveltejs/kit": "^2.5.0",
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"@sveltejs/vite-plugin-svelte": "^4.0.0",
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"svelte": "^5.0.0",
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"svelte-check": "^4.0.0",
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"typescript": "^5.5.0",
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"vite": "^5.4.0",
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"vitest": "^2.0.0"
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}
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}
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