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Clinical-Genomics / cg / 14516791844
86%
master: 78%

Build:
Build:
LAST BUILD BRANCH: 4794-nallo-upload-chromograph
DEFAULT BRANCH: master
Ran 17 Apr 2025 01:30PM UTC
Jobs 1
Files 824
Run time 3min
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17 Apr 2025 01:27PM UTC coverage: 85.561%. First build
14516791844

Pull #4330

github

web-flow
Merge 51474df2a into ab107e1a9
Pull Request #4330: RAREDISEASE & nf-analysis: change logic for skip_germlinevariant calling in config-case

10 of 11 new or added lines in 3 files covered. (90.91%)

26358 of 30806 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 14516791844.1 17 Apr 2025 01:30PM UTC 824
85.56
GitHub Action Run
Source Files on build 14516791844
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  • List 824
  • 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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