Closed jiaanqiang closed 2 months ago
I have only R1.fastq, R2.fastq, genome.fa, and genome.gtf files.
Arriba can be run without the missing files. You will have more false positives, however (especially read-through transcripts).
Just run the script run_arriba.sh
with empty files for the ones that you don't have. Alternatively, you can run STAR manually as shown in the script and then run arriba
with the following parameters: arriba -x Aligned.out.bam -o fusions.tsv -O fusions.discarded.tsv -a genome.fa -g genome.gtf -f blacklist
. Depending on how the chromosome are named, you will also need to adapt the value of the parameter -i
.
Thank you very much, it's working fine.
Thank you for developing such a user-friendly tool.
I want to use Arriba to identify gene fusions in plants, but I don't have the available blacklist.tsv, known_fusions.tsv, and protein_domains.gff3 files. I have only R1.fastq, R1.fastq, genome.fa, and genome.gtf files. What command should I use to execute this task?