CLI Reference¶
The gbcms command-line interface provides a single powerful command for variant counting.
Commands¶
| Command | Description |
|---|---|
| run | Count alleles at variant positions |
Quick Example¶
gbcms run \
--variants mutations.maf \
--bam sample1:sample1.bam \
--bam sample2:sample2.bam \
--fasta reference.fa \
--output-dir results/
Getting Help¶
Related¶
- Quick Start — Common usage patterns
- Nextflow Pipeline — For processing many samples
- Input Formats — VCF/MAF specifications
abbreviations