Provided by: subread_1.6.3+dfsg-1_amd64
subjunc - an RNA-seq aligner suitable for all purposes of RNA-seq analyses
subjunc [options] -i <index_name> -r <input> -o <output> ## Mandatory arguments: -i <index> Base name of the index. -r <string> Name of an input read file. If paired-end, this should be the first read file (typically containing "R1"in the file name) and the second should be provided via "-R". Acceptable formats include gzipped FASTQ, FASTQ and FASTA. These formats are identified automatically. ## Optional arguments: # input reads and output -o <string> Name of an output file. By default, the output is in BAM format. Omitting this option makes the output be written to STDOUT. -R <string> Name of the second read file in paired-end data (typically containing "R2" the file name). --SAMinput Input reads are in SAM format. --BAMinput Input reads are in BAM format. --SAMoutput Save mapping results in SAM format. # Phred offset -P <3:6> Offset value added to the Phred quality score of each read base. '3' for phred+33 and '6' for phred+64. '3' by default. # thresholds for mapping -n <int> Number of selected subreads, 14 by default. -m <int> Consensus threshold for reporting a hit (minimal number of subreads that map in consensus) . If paired-end, this gives the consensus threshold for the anchor read (anchor read receives more votes than the other read in the same pair). 1 by default. -p <int> Consensus threshold for the non- anchor read in a pair. 1 by default. -M <int> Maximum number of mis-matched bases allowed in each reported alignment. 3 by default. Mis-matched bases found in softclipped bases are not counted. # unique mapping and multi-mapping --multiMapping Report multi-mapping reads in addition to uniquely mapped reads. Use "-B" to set the maximum number of equally-best alignments to be reported. -B <int> Maximum number of equally-best alignments to be reported for a multi-mapping read. Equally-best alignments have the same number of mis-matched bases. 1 by default. # indel detection -I <int> Maximum length (in bp) of indels that can be detected. 5 by default. Indels of up to 200bp long can be detected. --complexIndels Detect multiple short indels that are in close proximity (they can be as close as 1bp apart from each other). # read trimming --trim5 <int> Trim off <int> number of bases from 5' end of each read. 0 by default. --trim3 <int> Trim off <int> number of bases from 3' end of each read. 0 by default. # distance and orientation of paired end reads -d <int> Minimum fragment/insert length, 50bp by default. -D <int> Maximum fragment/insert length, 600bp by default. -S <ff:fr:rf> Orientation of first and second reads, 'fr' by default ( forward/reverse). # number of CPU threads -T <int> Number of CPU threads used, 1 by default. # read group --rg-id <string> Add read group ID to the output. --rg <string> Add <tag:value> to the read group (RG) header in the output. # read order --keepReadOrder Keep order of reads in BAM output the same as that in the input file. Reads from the same pair are always placed next to each other no matter this option is specified or not. --sortReadsByCoordinates Output location-sorted reads. This option is applicable for BAM output only. A BAI index file is also generated for each BAM file so the BAM files can be directly loaded into a genome browser. # color space reads -b Convert color-space read bases to base-space read bases in the mapping output. Note that read mapping is performed at color-space. # dynamic programming --DPGapOpen <int> Penalty for gap opening in short indel detection. -1 by default. --DPGapExt <int> Penalty for gap extension in short indel detection. 0 by default. --DPMismatch <int> Penalty for mismatches in short indel detection. 0 by default. --DPMatch <int> Score for matched bases in short indel detection. 2 by default. # detect all junctions including gene fusions --allJunctions Detect exon-exon junctions (both canonical and non-canonical junctions) and structural variants in RNA-seq data. Refer to Users Guide for reporting of junctions and fusions. # gene annotation -a Name of an annotation file (gzipped file is accepted). GTF/GFF format by default. See -F option for more format information. -F Specify format of the provided annotation file. Acceptable formats include 'GTF' (or compatible GFF format) and 'SAF'. 'GTF' by default. For SAF format, please refer to Users Guide. -A Provide a chromosome name alias file to match chr names in annotation with those in the reads. This should be a twocolumn comma-delimited text file. Its first column should include chr names in the annotation and its second column should include chr names in the index. Chr names are case sensitive. No column header should be included in the file. --gtfFeature <string> Specify feature type in GTF annotation. 'exon' by default. Features used for read counting will be extracted from annotation using the provided value. --gtfAttr <string> Specify attribute type in GTF annotation. 'gene_id' by default. Meta-features used for read counting will be extracted from annotation using the provided value. # others -v Output version of the program. Refer to Users Manual for detailed description to the arguments.