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Clinical-Genomics / cg / 18273290355
86%

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DEFAULT BRANCH: master
Ran 06 Oct 2025 07:29AM UTC
Jobs 1
Files 875
Run time 2min
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06 Oct 2025 07:26AM UTC coverage: 86.132% (+0.1%) from 86.032%
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(Pipeline integration) dev Refactor start MIP-DNA (patch)

Reworks the starting of MIP-DNA to use the AnalysisStarter. Introduces new commands `dev-start`, `dev-run` and `dev-config-case`. The new commands do not have separate `dev-panel` and `dev-managed-variants` commands, since they are a part of the `dev-config-case` command. Closes https://github.com/Clinical-Genomics/pipeline-integration/issues/46.

### Added

- cg workflow mip-dna dev-start
- cg workflow mip-dna dev-run
- cg workflow mip-dna dev-config-case

### Changed

- 

### Fixed

- New lines are added in the managed_variants and gene panel files which were previously malformed for the raredisease dev commands

---------

Co-authored-by: Sebastian Diaz <juan.sebastian.diaz.boada@scilifelab.se>
Co-authored-by: Isak Ohlsson Ångnell <40887124+islean@users.noreply.github.com>
Co-authored-by: Rasmus Burge <80392398+RasmusBurge-CG@users.noreply.github.com>
Co-authored-by: islean <isak.ohlsson.angnell@gmail.com>

353 of 360 new or added lines in 32 files covered. (98.06%)

1 existing line in 1 file now uncovered.

27838 of 32320 relevant lines covered (86.13%)

0.86 hits per line

New Missed Lines in Diff

Lines Coverage ∆ File
3
32.53
-0.11% cg/apps/lims/api.py
4
94.3
-0.58% cg/store/crud/read.py

Uncovered Existing Lines

Lines Coverage ∆ File
1
98.08
4.53% cg/services/analysis_starter/configurator/file_creators/nextflow/params_file/raredisease.py
Jobs
ID Job ID Ran Files Coverage
1 18273290355.1 06 Oct 2025 07:29AM UTC 875
86.13
GitHub Action Run
Source Files on build 18273290355
  • Tree
  • List 875
  • Changed 23
  • Source Changed 0
  • Coverage Changed 23
Coverage ∆ File Lines Relevant Covered Missed Hits/Line
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