arriba
Identify fusion genes in paired-read RNA sequencing BAM files using Arriba
usage
nexus run --nf-workflow variant_calling_arriba.nf \
-c nextflow.config \
-w work/ \
--samples_tsv_file samples.tsv \
--output_dir results/ \
--reference_genome_fasta_file /path/to/file.fasta \
--reference_genes_gtf_file /path/to/file.gtf \
--protein_domains_gff3_file /path/to/file \
--params_arriba "-S 3 -f blacklist -i chr*"
Note
Nextflow config files are available here. Use the config file that matches your installed nexus version (e.g. nexus_v0.2.0_nextflow_slurm.config).
parameters
| parameter | description |
|---|---|
--samples_tsv_file |
TSV file with the following columns: ‘sample_id’, ‘bam_file’, ‘bam_bai_file’. |
--output_dir |
Directory to which output files will be copied. |
--reference_genome_fasta_file |
Reference genome FASTA file. |
--reference_genes_gtf_file |
Reference genes GTF file. |
--protein_domains_gff3_file |
Protein domains GFF3 file. |
--params_arriba |
Arriba parameters (default: ’“-S 3 -f blacklist -i chr*“’). Note that the parameters need to be wrapped in quotes. |