Initial release: rarelens platform skeleton (AGPL-3.0)
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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.
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apiVersion: networking.k8s.io/v1
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kind: Ingress
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metadata: { name: rarelens }
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spec:
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rules:
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- http:
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paths:
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- { path: /api, pathType: Prefix, backend: { service: { name: api, port: { number: 80 } } } }
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- { path: /, pathType: Prefix, backend: { service: { name: web, port: { number: 80 } } } }
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