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.
8 lines
192 B
JavaScript
8 lines
192 B
JavaScript
import adapter from '@sveltejs/adapter-node';
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import { vitePreprocess } from '@sveltejs/vite-plugin-svelte';
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export default {
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preprocess: vitePreprocess(),
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kit: { adapter: adapter() }
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};
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