referenceFasta: {description: "Genome reference to use", category: "required"}
referenceFastaIndex: {description: "Index for the genome reference file.", category: "required"}
inputBam: {description: "Aligned, sorted, indexed BAM file containing the reads we want to call.", category: "required"}
inputBamIndex: {description: "Index for the input bam file.", category: "required"}
modelType: {description: "<WGS|WES|PACBIO>. Type of model to use for variant calling. Each model_type has an associated default model, which can be overridden by the --customized_model flag", category: "required"}
outputVcf: {description: "Path where we should write VCF file.", category: "required"}
customizedModel: {description: "A path to a model checkpoint to load for the `call_variants` step. If not set, the default for each --model_type will be used", category: "advanced"}
numShards: {description: "Number of shards for make_examples step.", category: "common"}
outputGVcf: {description: "Path where we should write gVCF file.", category: "common"}
regions: {description: "List of regions we want to process, in BED/BEDPE format.", category: "advanced"}
sampleName: {description: "Sample name to use instead of the sample name from the input reads BAM (SM tag in the header).", category: "common"}
VCFStatsReport: {description: "Output a visual report (HTML) of statistics about the output VCF.", category: "common"}
memory: {description: "The amount of memory this job will use.", category: "advanced"}
timeMinutes: {description: "The maximum amount of time the job will run in minutes.", category: "advanced"}
dockerImage: {description: "The docker image used for this task. Changing this may result in errors which the developers may choose not to address.",