A list of all possible parameter that can be used for the different scripts included in Sarek.
Display help
Disable all QC tools and MultiQC.
Choose an output directory
Specify a project number ID on a UPPMAX cluster. (optional if not on such a cluster)
Specify wich mode publishDir directive need to follow, in Sarek link is the default mode.
From Nextflow documentation:
| Mode | Description |
|---|---|
| copy | Copies the output files into the published directory |
| copyNoFollow | Copies the output files into the published directory without following symlinks ie. copies the links themselves |
| link | Creates a hard link in the published directory for each process output file (default) |
| move | Moves the output files into the published directory. Note: this is only supposed to be used for a terminating process i.e. a process whose output is not consumed by any other downstream process |
| rellink | Creates a relative symbolic link in the published directory for each process output file |
| symlink | Creates an absolute symbolic link in the published directory for each process output file |
Use the given TSV file as sample (cf TSV documentation).
Is not used for annotate.nf and runMultiQC.nf.
Choose which tools will be used in the workflow. Different tools to be separated by commas. Possible values are:
- haplotypecaller (use
HaplotypeCallerfor VC) (germlineVC.nf) - manta (use
Mantafor SV) (germlineVC.nf,somaticVC.nf) - strelka (use
Strelkafor VC) (germlineVC.nf,somaticVC.nf) - ascat (use
ASCATfor CNV) (somaticVC.nf) - mutect2 (use
MuTect2for VC) (somaticVC.nf) - snpeff (use
snpEfffor Annotation) (annotate.nf) - vep (use
VEPfor Annotation) (annotate.nf)
--tools option is case insensitive to avoid easy introduction of errors when choosing tools.
So you can write --tools mutect2,ascat or --tools MuTect2,ASCAT without worrying about case sensitivity.
Display more information about files being processed.
Choose from wich step the workflow will start. Choose only one step. Possible values are:
- mapping (default, will start workflow with FASTQ files)
- recalibrate (will start workflow with BAM files and Recalibration Tables
--step option is case insensitive to avoid easy introduction of errors when choosing a step.
Test run Sarek on a smaller dataset, that way you don't have to specify --sample Sarek-data/testdata/tsv/tiny.tsv
Run only QC tools and MultiQC to generate a HTML report.
Choose which tools to annotate. Different tools to be separated by commas. Possible values are:
- haplotypecaller (Annotate
HaplotypeCalleroutput) - manta (Annotate
Mantaoutput) - mutect2 (Annotate
MuTect2output) - strelka (Annotate
Strelkaoutput)
Choose vcf to annotate. Different vcfs to be separated by commas.
Specify a name for MultiQC report (optional)
Specify an email for MultiQC report (optional)
For most use cases, the reference information is already in the configuration file conf/genomes.config.
However, if needed, you can specify any reference file at the command line.
For most use cases, the reference information is already in the appropriate configuration files. However, it is still possible to specify these parameters at the command line as well.