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
214 B
Plaintext
14 lines
214 B
Plaintext
process LOAD_DB {
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tag "$job_id"
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input:
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path tsv
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val job_id
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val db_url
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output: stdout
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script:
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"""
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load_db.py --tsv $tsv --job-id $job_id --db-url '$db_url'
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"""
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}
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