.\" DO NOT MODIFY THIS FILE! It was generated by help2man 1.47.16. .TH STRINGTIE "1" "November 2020" "stringtie 2.1.4" "User Commands" .SH NAME stringtie \- StringTie .SH DESCRIPTION StringTie v2.1.4 usage: .PP stringtie [\-G ] [\-l ] [\-o ] [\-p ] .IP [\-v] [\-a ] [\-m ] [\-j ] [\-f ] [\-c ] [\-g ] [\-u] [\-L] [\-e] [\-\-viral] [\-E ] [\-\-ptf ] [\-x ] [\-A ] [\-h] {\-B|\-b } .PP Assemble RNA\-Seq alignments into potential transcripts. Options: .HP \fB\-\-version\fR : print just the version at stdout and exit .HP \fB\-\-conservative\fR : conservative transcript assembly, same as \fB\-t\fR \fB\-c\fR 1.5 \fB\-f\fR 0.05 .HP \fB\-\-rf\fR : assume stranded library fr\-firststrand .HP \fB\-\-fr\fR : assume stranded library fr\-secondstrand .HP \fB\-G\fR reference annotation to use for guiding the assembly process (GTF/GFF3) .HP \fB\-\-ptf\fR : load point\-features from a given 4 column feature file .HP \fB\-o\fR output path/file name for the assembled transcripts GTF (default: stdout) .HP \fB\-l\fR name prefix for output transcripts (default: STRG) .HP \fB\-f\fR minimum isoform fraction (default: 0.01) .HP \fB\-L\fR long reads processing; also enforces \fB\-s\fR 1.5 \fB\-g\fR 0 (default:false) .HP \fB\-R\fR if long reads are provided, just clean and collapse the reads but .IP do not assemble .HP \fB\-m\fR minimum assembled transcript length (default: 200) .HP \fB\-a\fR minimum anchor length for junctions (default: 10) .HP \fB\-j\fR minimum junction coverage (default: 1) .HP \fB\-t\fR disable trimming of predicted transcripts based on coverage .IP (default: coverage trimming is enabled) .HP \fB\-c\fR minimum reads per bp coverage to consider for multi\-exon transcript .IP (default: 1) .HP \fB\-s\fR minimum reads per bp coverage to consider for single\-exon transcript .IP (default: 4.75) .HP \fB\-v\fR verbose (log bundle processing details) .HP \fB\-g\fR maximum gap allowed between read mappings (default: 50) .HP \fB\-M\fR fraction of bundle allowed to be covered by multi\-hit reads (default:1) .HP \fB\-p\fR number of threads (CPUs) to use (default: 1) .HP \fB\-A\fR gene abundance estimation output file .HP \fB\-E\fR define window around possibly erroneous splice sites from long reads to .IP look out for correct splice sites (default: 25) .HP \fB\-B\fR enable output of Ballgown table files which will be created in the .IP same directory as the output GTF (requires \fB\-G\fR, \fB\-o\fR recommended) .HP \fB\-b\fR enable output of Ballgown table files but these files will be .IP created under the directory path given as .HP \fB\-e\fR only estimate the abundance of given reference transcripts (requires \fB\-G\fR) .HP \fB\-\-viral\fR : only relevant for long reads from viral data where splice sites .IP do not follow consensus (default:false) .HP \fB\-x\fR do not assemble any transcripts on the given reference sequence(s) .HP \fB\-u\fR no multi\-mapping correction (default: correction enabled) .HP \fB\-h\fR print this usage message and exit .SS "Transcript merge usage mode:" .IP stringtie \fB\-\-merge\fR [Options] { gtf_list | strg1.gtf ...} .PP With this option StringTie will assemble transcripts from multiple input files generating a unified non\-redundant set of isoforms. In this mode the following options are available: .TP \fB\-G\fR reference annotation to include in the merging (GTF/GFF3) .TP \fB\-o\fR output file name for the merged transcripts GTF (default: stdout) .TP \fB\-m\fR minimum input transcript length to include in the merge (default: 50) .TP \fB\-c\fR minimum input transcript coverage to include in the merge (default: 0) .TP \fB\-F\fR minimum input transcript FPKM to include in the merge (default: 1.0) .TP \fB\-T\fR minimum input transcript TPM to include in the merge (default: 1.0) .TP \fB\-f\fR minimum isoform fraction (default: 0.01) .TP \fB\-g\fR gap between transcripts to merge together (default: 250) .TP \fB\-i\fR keep merged transcripts with retained introns; by default these are not kept unless there is strong evidence for them .TP \fB\-l\fR