StringTie-Teaching

Category

Bioinformatics

Program On

Teaching

Version

2.1.1

Author / Distributor

StringTie

Description

"StringTie is a fast and highly efficient assembler of RNA-Seq alignments into potential transcripts." More details are at StringTie

Running Program

Version 2.1.1 of this application is in /apps/eb/StringTie/2.1.1-GCC-8.3.0

To use this version, please load the module with

ml StringTie/2.1.1-GCC-8.3.0

Here is an example of a shell script, sub.sh, to run on the batch queue:

#!/bin/bash
#SBATCH --job-name=j_StringTie
#SBATCH --partition=batch
#SBATCH --mail-type=ALL
#SBATCH --mail-user=username@uga.edu
#SBATCH --ntasks=1
#SBATCH --mem=10gb
#SBATCH --time=08:00:00
#SBATCH --output=StringTie.%j.out
#SBATCH --error=StringTie.%j.err

cd $SLURM_SUBMIT_DIR
ml StringTie/2.1.1-GCC-8.3.0
stringtie [options]

In the real submission script, at least all the above underlined values need to be reviewed or to be replaced by the proper values.

Please refer to Running_Jobs_on_the_teaching_cluster, Run X window Jobs and Run interactive Jobs for more details of running jobs at Teaching cluster.

Here is an example of job submission command:

sbatch ./sub.sh 

Documentation

ml StringTie/2.1.1-GCC-8.3.0

stringtie --help
StringTie v2.1.1 usage:
 stringtie <input.bam ..> [-G <guide_gff>] [-l <label>] [-o <out_gtf>] [-p <cpus>]
  [-v] [-a <min_anchor_len>] [-m <min_tlen>] [-j <min_anchor_cov>] [-f <min_iso>]
  [-C <coverage_file_name>] [-c <min_bundle_cov>] [-g <bdist>] [-u] [-L]
  [-e] [-x <seqid,..>] [-A <gene_abund.out>] [-h] {-B | -b <dir_path>} 
Assemble RNA-Seq alignments into potential transcripts.
 Options:
 --version : print just the version at stdout and exit
 --conservative : conservative transcriptome assembly, same as -t -c 1.5 -f 0.05
 --rf assume stranded library fr-firststrand
 --fr assume stranded library fr-secondstrand
 -G reference annotation to use for guiding the assembly process (GTF/GFF3)
 -o output path/file name for the assembled transcripts GTF (default: stdout)
 -l name prefix for output transcripts (default: STRG)
 -f minimum isoform fraction (default: 0.01)
 -L use long reads settings (default:false)
 -R if long reads are provided, just clean and collapse the reads but do not assemble
 -m minimum assembled transcript length (default: 200)
 -a minimum anchor length for junctions (default: 10)
 -j minimum junction coverage (default: 1)
 -t disable trimming of predicted transcripts based on coverage
    (default: coverage trimming is enabled)
 -c minimum reads per bp coverage to consider for multi-exon transcript
    (default: 1)
 -s minimum reads per bp coverage to consider for single-exon transcript
    (default: 4.75)
 -v verbose (log bundle processing details)
 -g maximum gap allowed between read mappings (default: 50)
 -M fraction of bundle allowed to be covered by multi-hit reads (default:1)
 -p number of threads (CPUs) to use (default: 1)
 -A gene abundance estimation output file
 -B enable output of Ballgown table files which will be created in the
    same directory as the output GTF (requires -G, -o recommended)
 -b enable output of Ballgown table files but these files will be 
    created under the directory path given as <dir_path>
 -e only estimate the abundance of given reference transcripts (requires -G)
 -x do not assemble any transcripts on the given reference sequence(s)
 -u no multi-mapping correction (default: correction enabled)
 -h print this usage message and exit

Transcript merge usage mode: 
  stringtie --merge [Options] { gtf_list | strg1.gtf ...}
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:
  -G <guide_gff>   reference annotation to include in the merging (GTF/GFF3)
  -o <out_gtf>     output file name for the merged transcripts GTF
                    (default: stdout)
  -m <min_len>     minimum input transcript length to include in the merge
                    (default: 50)
  -c <min_cov>     minimum input transcript coverage to include in the merge
                    (default: 0)
  -F <min_fpkm>    minimum input transcript FPKM to include in the merge
                    (default: 1.0)
  -T <min_tpm>     minimum input transcript TPM to include in the merge
                    (default: 1.0)
  -f <min_iso>     minimum isoform fraction (default: 0.01)
  -g <gap_len>     gap between transcripts to merge together (default: 250)
  -i               keep merged transcripts with retained introns; by default
                   these are not kept unless there is strong evidence for them
  -l <label>       name prefix for output transcripts (default: MSTRG)

Back to Top

Installation

Source code is obtained from StringTie

System

64-bit Linux