nanocaller

Identify germline small DNA variants in long-read DNA sequencing BAM files using NanoCaller

usage

nexus run --nf-workflow variant_calling_nanocaller.nf \
    -c nextflow.config \
    -w work/ \
    --samples_tsv_file samples.tsv \
    --output_dir results/ \
    --reference_genome_fasta_file /path/to/file.fasta \
    --params_nanocaller "--preset ont --mode all --sequencing ont --phase --enable_whatshap"

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.
--params_nanocaller	NanoCaller parameters (default: ‘“–preset ont –mode all –sequencing ont –phase –enable_whatshap”’). Note that the parameters need to be wrapped in quotes.