sqanti3-fasta
Characterize isoforms using Sqanti3 (FASTA mode)
usage
nexus run --nf-workflow isoform_characterization_sqanti3-fasta.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 \
--params_sqanti3_qc "--aligner_choice minimap2 --report html --force_id_ignore" \
--params_sqanti3_filter "ml"
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’, ‘fasta_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. |
--params_sqanti3_qc |
sqanti3_qc.py parameters (default: ‘“–aligner_choice minimap2 –report html –force_id_ignore –isoAnnotLite”’). Note that the parameters need to be wrapped in quotes. |
--params_sqanti3_filter |
sqanti3_filter.py parameters (default: ‘“ml”’). Note that the parameters need to be wrapped in quotes. |