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.
14 lines
422 B
YAML
14 lines
422 B
YAML
apiVersion: argoproj.io/v1alpha1
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kind: Application
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metadata: { name: rarelens, namespace: argocd }
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spec:
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project: default
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source:
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repoURL: https://github.com/lynchaos/rarelens
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targetRevision: main
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path: infra/k8s/overlays/gcp
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destination: { server: https://kubernetes.default.svc, namespace: rarelens }
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syncPolicy:
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automated: { prune: true, selfHeal: true }
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syncOptions: [CreateNamespace=true]
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