kemal
5463f489a3
ci / api (push) Failing after 10s
ci / terraform (push) Failing after 11s
ci / web (push) Failing after 35s
ci / pipeline (push) Failing after 2m29s
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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.
10 lines
267 B
Terraform
10 lines
267 B
Terraform
variable "project" { type = string }
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variable "region" {
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type = string
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default = "europe-west2" # London: keeps public genomic test data and the Cambridge team in one jurisdiction
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}
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variable "github_repo" {
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type = string
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default = "lynchaos/rarelens"
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}
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