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Klinische Genetica
capture-lumc
vcf-to-varda
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c8d341f4a50684e265e1d5c6172597852cae0474
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Branches
2
master
default
protected
newerimages
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1
v1.0.0
3 results
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Created with Raphaël 2.2.0
29
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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
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
New client version.
Add info about token and input format.
Update varda2-client.
New version captures the whole response.
Moved to wrapper repo.
Merge branch 'master' of git.lumc.nl:klinische-genetica/capture-lumc/vcf-to-varda
Mark intermediate files as temporary so that they are removed.
Use a configuration file.
Script to create config from sample group info.
Parametrize meta data and enforce token env var.
Use rule dependency again.
Add submit to end of pipeline.
Use rule dependencies for output.
Run cthreepo last.
Updated versions of containers.
Rule dependencies.
Rename rules and add comments.
Use constants for containers.
Initial version of preprocessing pipeline.
Token commit.
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