Initial release: rarelens platform skeleton (AGPL-3.0)

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.

web/svelte.config.js

@@ -0,0 +1,7 @@
+import adapter from '@sveltejs/adapter-node';
+import { vitePreprocess } from '@sveltejs/vite-plugin-svelte';
+
+export default {
+  preprocess: vitePreprocess(),
+  kit: { adapter: adapter() }
+};