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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 / 22345871733
86%
master: 86%

Build:
Build:
LAST BUILD BRANCH: add-balsamic-cache-to-config
DEFAULT BRANCH: master
Ran 24 Feb 2026 10:04AM UTC
Jobs 1
Files 886
Run time 1min
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24 Feb 2026 10:01AM UTC coverage: 86.449%. First build
22345871733

Pull #4871

github

web-flow
Merge 91b39ad62 into 2c7a92db0
Pull Request #4871: DEV - Switch reference genome to hg38 for raredisease

82 of 83 new or added lines in 18 files covered. (98.8%)

28267 of 32698 relevant lines covered (86.45%)

0.86 hits per line

New Missed Lines in Diff

Lines Coverage ∆ File
1
97.3
cg/services/analysis_starter/configurator/file_creators/nextflow/params_file/raredisease_params_file_creator.py
Jobs
ID Job ID Ran Files Coverage
1 22345871733.1 24 Feb 2026 10:04AM UTC 886
86.45
GitHub Action Run
Source Files on build 22345871733
  • Tree
  • List 886
  • Changed 0
  • Source Changed 0
  • Coverage Changed 0
Coverage ∆ File Lines Relevant Covered Missed Hits/Line
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  • Pull Request #4871
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