For instance:Īre two examples for potential lines in the feature file. Is the type of the feature (TSS or CPAS). The cromosome (sequence name, coordinate and strand), and the last The first three define the location of the point feature on There are four tab-delimited columns in the featureįile.
Loads a list of point-features from a text feature fileĪccepted point features are transcription start sites (TSS) and This option is required by options -B, -b, -e, -C (see below).Īssumes a stranded library fr-firststrand.Īssumes a stranded library fr-secondstrand. The output will include expressed reference transcripts as well as any novel transcripts that are assembled. Use a reference annotation file (in GTF or GFF3 format) to guide the assembly process. Specify the number of processing threads (CPUs) to use for transcript assembly.
#Si string section manual full
This can be specified as a full path, in which case directories will be created as needed.īy default StringTie writes the GTF at standard output. Sets the name of the output GTF file where StringTie will write the assembled transcripts. Turns on verbose mode, printing bundle processing details. The processing of read alignments to estimating the coverage of the transcripts given with the -G option This option directs StringTie to operate in expression estimation mode this limits Mixed reads processing mode both short and long read data alignmentsĪre expected (long read alignments must be given as the 2nd BAM/CRAM input file) Long reads processing mode also enforces -s 1.5 -g 0 (default:false) The following optional parameters can be specified when running stringtie: Other options - the following command line is equivalent to the one above: With the other options of the program, so the input alignment files can also precede or be given in between the Note that the command line parser in StringTie allows arbitrary order and mixing of the positional parameters Both alignment files must be sorted by genomic location. In a specific order: the short read alignments must be the first file given while the long read alignments must be the second Note:if the -mix option is used, StringTie expects two alignment files to be given as positional parameters, Output (and can be captured into a file using the > output redirect operator). If this option is not used the output GTF records with the assembled transcripts will be printed to the standard The name of the output file should be specified with the -o option.
The main output is a GTF file containing the structural definitions of the transcripts assembled by Or the output of HISAT2 after sorting and converting it using samtools Read alignments sorted by their genomic location (for example the accepted_hits.bam file produced by TopHat The main input of the program ( ) must be a SAM, BAM or CRAM file with RNA-Seq The generic command line for the default usage has this format::