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nf-cmgg / structural

A bioinformatics best-practice analysis pipeline for calling structural variants (SVs), copy number variants (CNVs) and repeat region expansions (RREs) from short DNA reads
https://nf-cmgg.github.io/structural/
MIT License
18 stars 3 forks source link

v0.1.0 pipeline release #80

Closed nvnieuwk closed 5 months ago

nvnieuwk commented 5 months ago

This PR contains all changes made for the v0.1.0 release of the pipeline, not all files should be reviewed since these changes have all been reviewed when merging to dev

nvnieuwk commented 5 months ago

Hallelujah! I'll wait until all tests pass and then I'll merge and release

mvheetve commented 5 months ago

[celebrate] Mattias Van Heetvelde reacted to your message:

From: Nicolas Vannieuwkerke @.> Sent: Wednesday, April 3, 2024 12:52:40 PM To: nf-cmgg/structural @.> Cc: Mattias Van Heetvelde @.>; Review requested @.> Subject: Re: [nf-cmgg/structural] v0.1.0 pipeline release (PR #80)

Hallelujah! I'll wait until all tests pass and then I'll merge and release

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