Add script to run Nextflow configuration regression tests locally #23
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Description
This PR adds a new
nfconfigtest
script that allows users to run the regression tests locally:The script automatically cleans up any of the
-out.json
files that do match the expected results, leaving only the files that a user needs to review.In addition to the script itself, I changed the
sed
command in the Dockerfile to be a little more robust. The launcher script for Nextflow 24.01.0-edge no longer has double quotes (I'm assuming just to thwart me specifically), so this is just a bit of future-proofing.Checklist
This PR does NOT contain Protected Health Information (PHI). A repo may need to be deleted if such data is uploaded.
Disclosing PHI is a major problem1 - Even a small leak can be costly2.
This PR does NOT contain germline genetic data3, RNA-Seq, DNA methylation, microbiome or other molecular data4.
.png
, .jpeg
),.pdf
,.RData
,.xlsx
,.doc
,.ppt
, or other output files.To automatically exclude such files using a .gitignore file, see here for example.
I have read the code review guidelines and the code review best practice on GitHub check-list.
I have set up or verified the
main
branch protection rule following the github standards before opening this pull request.The name of the branch is meaningful and well formatted following the standards, using [AD_username (or 5 letters of AD if AD is too long)]-[brief_description_of_branch].
I have added the major changes included in this pull request to the
CHANGELOG.md
under the next release version or unreleased, and updated the date.Footnotes
UCLA Health reaches $7.5m settlement over 2015 breach of 4.5m patient records ↩
The average healthcare data breach costs $2.2 million, despite the majority of breaches releasing fewer than 500 records. ↩
Genetic information is considered PHI.
Forensic assays can identify patients with as few as 21 SNPs ↩
RNA-Seq, DNA methylation, microbiome, or other molecular data can be used to predict genotypes (PHI) and reveal a patient's identity. ↩