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Warning: This build has drifted.
The coverage report for this pull request build may be inaccurate because its base commit is no longer the HEAD of its target branch.
This means it includes changes from outside the original pull request, including, potentially, unrelated coverage changes.

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Clinical-Genomics / cg / 14706305816
86%
master: 78%

Build:
Build:
LAST BUILD BRANCH: 4794-nallo-upload-chromograph
DEFAULT BRANCH: master
Ran 28 Apr 2025 11:12AM UTC
Jobs 1
Files 829
Run time 1min
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28 Apr 2025 11:09AM UTC coverage: 85.604% (+4.2%) from 81.365%
14706305816

Pull #4330

github

web-flow
Merge 1d917ff4e into 908d1b5c1
Pull Request #4330: RAREDISEASE & nf-analysis: change logic for skip_germlinevariant calling in config-case

6 of 7 new or added lines in 2 files covered. (85.71%)

26437 of 30883 relevant lines covered (85.6%)

0.86 hits per line

New Missed Lines in Diff

Lines Coverage ∆ File
1
88.75
-0.12% cg/meta/workflow/nf_analysis.py
Jobs
ID Job ID Ran Files Coverage
1 14706305816.1 28 Apr 2025 11:12AM UTC 829
85.6
GitHub Action Run
Source Files on build 14706305816
  • Tree
  • List 829
  • Changed 0
  • Source Changed 0
  • Coverage Changed 0
Coverage ∆ File Lines Relevant Covered Missed Hits/Line
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  • Pull Request #4330
  • PR Base - master (#14706339664)
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