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Clinical-Genomics / cg / 14642428157
86%
master: 78%

Build:
Build:
LAST BUILD BRANCH: 4794-nallo-upload-chromograph
DEFAULT BRANCH: master
Ran 24 Apr 2025 01:11PM UTC
Jobs 1
Files 829
Run time 26min
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24 Apr 2025 01:08PM UTC coverage: 85.603%. First build
14642428157

Pull #4330

github

web-flow
Merge 09d986e54 into 99be0052c
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%)

26436 of 30882 relevant lines covered (85.6%)

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 14642428157.1 24 Apr 2025 01:11PM UTC 829
85.6
GitHub Action Run
Source Files on build 14642428157
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  • 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
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