Alternative splicing tools parameters
Found in file: scripts/asevent_config.sh
This config file sets parameters that are specific to AS event detection tools only.
Basic Parameters
- transcript
- Fasta file for gene transcripts.
- star_alignment_files
- Path to the folder containing star alignment files (*.SJ.)Default:
$workdir/output/star-output
Note
We support only paired RNA-Seq - fastq files have to be in pairs.
Set the suffixes parameters (including the file extension) for all fastq pairs (e.g.
_1.fastq
and _2.fastq
).- fastqpair1suffix
- Suffix for the first file of the fastq pair.Example:
_1.fastq
- fastqpair2suffix
- Suffix for the second file of the fastq pair.Example:
_2.fastq
- use_bam_input_files
- Determines what kind of input to use:
1
for bam files,0
for fastq files.Default:0
- combine_events
- Events such as Multiple Exon Skipping should be represented as such, instead of individual exon skipping events.Default:
1
Warning
Something broke while changing the config file? Make sure there is no space between the variable, the equal sign and the value.
Since these files are bash scripts, it is important to mind the syntax rules. E.g., there can’t be a whitespace before and after “=”.
For example: | Wrong: workdir = “dockers/” | Right: workdir=”dockers/”