ngs-pl run-targeted-variant-caller ================================== Synopsis -------- **ngs-pl run-targeted-variant-caller** -o/--outdir *OUTDIR* [--snakefile] [--panel] [-t/--target] [-p/--paired] [-s/--single] [-u/--underscore] *INPUTFILES* Description ----------- :program:`ngs-pl run-targeted-variant-caller` runs targeted variant calling workflow to produce single-sample VCF file for each sample. Each VCF file will then be merged into a multi-sample VCF file when ``--target`` is set to ``merged_vcf``. Options ------- .. program:: ngs-pl run-targeted-variant-caller .. option:: -h, --help Show this help message and exit. .. option:: -o, --outdir OUTDIR Output directory to create the symbolic links. .. option:: --debug Enable debug mode for detailed logging. .. option:: --snakefile Snakefile to use for the workflow. When supplied without absolute or relative path, the snakefile will be looked up from the available snakefiles included with the pipeline. See the configuration section below for the list of available snakefiles. .. option:: -t, --target Set the target of the workflow. Available targets depend on the used snakefile, see the configuration section below. Configurations -------------- .. option:: targeted_variant_caller_wf Snakemake workflow file (snakefile) to run. Available snakefiles are: msf_panel_varcall_lr.smk This is the workflow for panel variant calling using singleton long reads from ONT or PacBio. Available targets are: merged_vcf This results in a multi-sample VCF file as VCF files from each sample is merged using ``bcftools merge`` command. merged_report This results in a Excel file containing report of genotypes of each sample. msf_panel_varcall_pe.smk This is the workflow panel variant calling using paired-end short reads from Illumina platforms. Available targets are the same as msf_panel_varcall_lr.smk above .. option:: target The targets will be specific to each of snakefile. See the snakefile above to get the available targets.