Releases: molgenis/molgenis-pipelines
Releases · molgenis/molgenis-pipelines
DNA pipeline 3.1.0 (Bison)
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- Added Delly to pipeline
- Major bug fix in Sex chromosome calling
DNA pipeline 3.0.2 (Armadillo)
Put quotes around variables in comparisons
DNA pipeline 3.0.1 (Armadillo)
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Pipeline is in principle the same as 2.1.2.
Major change:
Pipeline is now ready to work with Slurm and can be used in the new environment (calculon,zinc-finger etc).
- changed parameter file + generate template
- updated tool versions
Small fixes/changes:
- updated batchsize (batches were too big and with gVCF the need for a big batch size is not necessary)
- added environment specific parameter files
- fixed CopyToResults dir bug (.finished file was written on the wrong place)
NGS_DNA-2.1.2 pipeline
Implemented gVCF variant calling + minor bugfixes
DNA pipeline 2.1.1
Big changes has been made, most important change is that VariantCalling. VariantCalling will now be done per project instead of per sample.
new protocols:
- Sequenom concordance check
- CheckSex (there is a check whether a sample is male or female)
- PhiX virus reads are added to each sample. This is done to check if the pipeline ran correctly.
- CoveragePerBase (This is a request of the Diagnostics department). This will only be done on targeted panels and SSID kit samples.
updates:
- VariantCalling is now per project instead of per sample. It is now better visible in the vcf's whether a SNP/Indel was of bad quality or it is homozygous reference call
- ChrParameters is now replaced by batching (50, 200 or 500 batches). This will decrease the running time of the VariantCalling
DNA pipeline 2.0.1
bugfixes to
- loading correct molgenis version in CreateInhouseProjects.sh
- removed unused pindelOutputVcf variable
- changed name of file (without the chr)
DNA pipeline 2.0
Merge pull request #196 from Gerbenvandervries/master added README.txt, and clean protocols for versionNumber and allOutputExi...
gpfs-pipelines
pipelines suitable for old gpfs structure