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: apps/v1
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kind: Deployment
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metadata: { name: web }
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spec:
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replicas: 2
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selector: { matchLabels: { app: web } }
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template:
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metadata: { labels: { app: web } }
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spec:
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containers:
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- name: web
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image: rarelens/web
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ports: [{ containerPort: 3000 }]
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env: [{ name: PUBLIC_API_URL, value: /api }]
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resources: { requests: { cpu: 100m, memory: 128Mi }, limits: { cpu: 500m, memory: 256Mi } }
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---
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apiVersion: v1
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kind: Service
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metadata: { name: web }
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spec: { selector: { app: web }, ports: [{ port: 80, targetPort: 3000 }] }
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