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Klinische Genetica
capture-lumc
vcf-to-varda
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017fa3ca7d3dc6dd4746d54e8b004059dc2d9426
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Branches
2
master
default
protected
newerimages
Tags
1
v1.0.0
3 results
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Created with Raphaël 2.2.0
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1
Use an image where the extra line bug is fixed
newerimages
newerimages
Remove effect of rogue print statement
Update vcf2variants command line
Use newer images
Merge branch 'fix-tests' into 'master'
master
master
Make environment really specific
Activate the environment after installing it
Install the conda environment when it is not present
Remove local rules
v1.0.0
v1.0.0
Merge branch '1-disease-code-can-be-n' into 'master'
Update path to test config
Add test for newline as disease code
Add quotes around disease code
Merge branch 'client_0.9' into 'master'
Use latest version of varda2-client.
Merge branch 'devel' into 'master'
Add tests for removal of ALTs that are not called
Write output to sample/varda folder
Add test for GIAB coverage
Add tests to check * variants are removed
Merge branch 'gitlab-ci' into devel
Add tests removing multiallelic ALTs
Keep temporary output files for testing
Add tests for removal of ALTs that are not called
Merge branch 'gitlab-ci' into 'devel'
Gitlab ci
Clean up vcf headers for test data
Add integration test
Remove basetemp from dry-run
Update script anchor
Execute dry-run tests on docker runner
Add test config
Add vcf-to-varda conda env
Run dry-run on the slurm runner
Keep workflow dir on failure
Add gitlab-ci file
Add initial pytest-workflow tests and data
Update snakemake to latest version
Add conda environment for the main pipeline
Merge branch 'master' of git.lumc.nl:klinische-genetica/capture-lumc/vcf-to-varda
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