UsageΒΆ

./MuSTA.R -h
usage: ./MuSTA.R [-h] [-v] -i INPUT -t GTF -g GENOME [-o OUTPUT] [-p PREFIX]
                 [--thread THREAD] [--copy-input] [--no-lordec] [--use-lq]
                 [--map-qual MAP_QUAL] [--salmon-ref] [--keep]
                 [--sqanti-filter SQANTI_FILTER] [--sqanti-qc SQANTI_QC]
                 [--lordec-build-SR-graph LORDEC_BUILD_SR_GRAPH]
                 [--lordec-correct LORDEC_CORRECT] [--minimap2 MINIMAP2]
                 [--samtools SAMTOOLS] [--salmon SALMON] [--seqkit SEQKIT]
                 [--os {6,7}] [--force] [--verbose] [--dry-run]

MuSTA v0.0.1: Multi-Sample Transcriptome Assembly

optional arguments:
  -h, --help            show this help message and exit
  -v, --version         show program's version number and exit

INPUT:
  -i INPUT, --input INPUT
                        An comma-separated file describing paths to input
                        files
  -t GTF, --gtf GTF     A gtf file of a reference transcriptome
  -g GENOME, --genome GENOME
                        A fasta file of a reference genome

OUTPUT:
  -o OUTPUT, --output OUTPUT
                        A directory where all outputs will be placed (default:
                        output)
  -p PREFIX, --prefix PREFIX
                        Prefix of result files (default: musta)

CONFIGULATION:
  --thread THREAD       Number of threads (default: 1)
  --copy-input          Copy input files to a temporary directory rather than
                        using them as is. This option is recommended when
                        input files are stored in external storage systems,
                        and In/Out load is troublesome
  --no-lordec           NOT run LoRDEC in order to correct long-read sequences
                        with RNA-seq reads
  --use-lq              Activate the {long_read_lq} field of the input config
                        file (for using polished_lq.fastq in addition to
                        polished_hq.fastq)
  --map-qual MAP_QUAL   A threshold of mapping quality. reads with quality
                        larger than this threshold are selected (default: 50)
  --salmon-ref          Run salmon against a reference gtf as well as against
                        a MuSTA-derived gtf
  --keep                Keep intermediate files

EXTERNAL SOFTWARES:
  This option group is need not to be specified unless you do not export
  external softwares in the Bash environment

  --sqanti-filter SQANTI_FILTER
                        Path to {sqanti_filter.py}
  --sqanti-qc SQANTI_QC
                        Path to {sqanti_qc.py}
  --lordec-build-SR-graph LORDEC_BUILD_SR_GRAPH
                        Path to {lordec-build-SR-graph}
  --lordec-correct LORDEC_CORRECT
                        Path to {lordec-correct}
  --minimap2 MINIMAP2   Path to {minimap2}
  --samtools SAMTOOLS   Path to {samtools}
  --salmon SALMON       Path to {salmon}
  --seqkit SEQKIT       Path to {seqkit}. This option is need not to be
                        specified unless you specify the {--no-lordec} option
                        and do not export {seqkit} in the Bash environment

MISCELLANEOUS:
  --os {6,7}            Redhat OS version for running qsub jobs. This option
                        is effective only on SHIROKANE super computer in Human
                        Genome Center, Japan (default: 7)
  --force               Re-run the entire pipeline, rather than resuming from
                        the suspended point of the last run.
  --verbose             Verbose mode
  --dry-run             Check the provided arguments but not run subprocesses.
                        All reports will be created in the current directory