Command-line options¶
The vip
command takes input vcf/cram/fastq data and produces a filtered annotated .vcf.gz
containing candidate variants of interest.
In addition to the .vcf.gz
an interactive .html
report is produced that can be displayed in any modern web browser.
vip --help
prints the available command-line options:
usage: vip -w <arg> -i <arg> -o <arg>
-w, --workflow <arg> workflow to execute. allowed values: cram, fastq, gvcf, vcf
-i, --input <arg> path to sample sheet .tsv
-o, --output <arg> output folder
-c, --config <arg> path to additional nextflow .cfg (optional)
-p, --profile <arg> nextflow configuration profile (optional)
-r, --resume resume execution using cached results (default: false)
-h, --help print this message and exit
Required¶
Optional¶
config
as described hereprofile
the configuration profile to use. allowed values arelocal
,slurm
plus any profiles added in--config
resume
useful to continue executions that was stopped by an error using cached results
Defaults¶
By default vip
:
- Assumes an Illumina sequencing platform was used to generate the input data
- Assumes whole-genome sequencing (WGS) method was used to generate the input data
- Uses a GRCh38 reference genome (GCA_000001405.15 / GCF_000001405.26)
- Provides classification trees for default variant filtration. For details, see here
- Creates reports using a default report template. For details, see here