• Home
  • Features
  • Pricing
  • Docs
  • Announcements
  • Sign In

Clinical-Genomics / cg / 14514806145
86%
master: 78%

Build:
Build:
LAST BUILD BRANCH: 4794-nallo-upload-chromograph
DEFAULT BRANCH: master
Ran 17 Apr 2025 11:42AM UTC
Jobs 1
Files 824
Run time 1min
Badge
Embed ▾
README BADGES
x

If you need to use a raster PNG badge, change the '.svg' to '.png' in the link

Markdown

Textile

RDoc

HTML

Rst

17 Apr 2025 11:39AM UTC coverage: 85.555%. First build
14514806145

Pull #4330

github

web-flow
Merge 32bca538a into ab107e1a9
Pull Request #4330: RAREDISEASE & nf-analysis: change logic for skip_germlinevariant calling in config-case

5 of 6 new or added lines in 2 files covered. (83.33%)

26363 of 30814 relevant lines covered (85.56%)

0.86 hits per line

New Missed Lines in Diff

Lines Coverage ∆ File
1
88.75
cg/meta/workflow/nf_analysis.py
Jobs
ID Job ID Ran Files Coverage
1 14514806145.1 17 Apr 2025 11:42AM UTC 824
85.56
GitHub Action Run
Source Files on build 14514806145
  • Tree
  • List 824
  • Changed 0
  • Source Changed 0
  • Coverage Changed 0
Coverage ∆ File Lines Relevant Covered Missed Hits/Line
  • Back to Repo
  • Pull Request #4330
STATUS · Troubleshooting · Open an Issue · Sales · Support · CAREERS · ENTERPRISE · START FREE · SCHEDULE DEMO
ANNOUNCEMENTS · TWITTER · TOS & SLA · Supported CI Services · What's a CI service? · Automated Testing

© 2026 Coveralls, Inc