Add instructions for README badges, update templates to major alias #20
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Description
This adds a fancy badge to the README showing the current GitHub release and linking to the release workflow:
It also adds instructions on how to add matching badges to calling repositories. Two points of frustration there:
Finally, I cleaned up the template workflows:
Secrets are only required until...
comments. It's just easier to keep using secrets.draft
parameter to the finalization workflow. Users copying the template can easily uncomment it, but it makes the drafting behavior opt-in.v1.0.0
tov1
. That'll eliminate the need for dependabot to bump anything except major versions. This is safe because it's our own workflow; any non-uclahs-cds
users of these workflows should stick with the full version.Closes #11
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. ↩