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
ci / images (api) (push) Skipped
ci / images (ml) (push) Skipped
ci / images (pipeline) (push) Skipped
ci / images (web) (push) Skipped
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.
18 lines
211 B
Plaintext
18 lines
211 B
Plaintext
__pycache__/
|
|
*.pyc
|
|
.venv/
|
|
.env
|
|
!web/.env
|
|
node_modules/
|
|
web/.svelte-kit/
|
|
web/build/
|
|
pipeline/work/
|
|
pipeline/.nextflow*
|
|
pipeline/results/
|
|
mlruns/
|
|
*.tfstate
|
|
*.tfstate.backup
|
|
.terraform/
|
|
data/*.vcf*
|
|
!data/README.md
|