lately I was trying you tool for rnaseq fusion detection.
I made a run with a pair-end bulk rnaseq sample (150bp) with 16 milions reads.
I used 16 threads and 64 GB of memory with the following command:
The run time is fairly normal. From the output, I see 87 calls, of which, 12 were labeled as HQ. You can also use the score column to filter to higher confidence calls.
Dear St.Jude Researchers,
lately I was trying you tool for rnaseq fusion detection. I made a run with a pair-end bulk rnaseq sample (150bp) with 16 milions reads. I used 16 threads and 64 GB of memory with the following command:
I takes a lot of time to finish 10 h 55 m 48 s.
Furthermore it gives me a huge rate of ambiguous calls. (I attached the output file)
Am I doing something wrong? Or it is normal?
Thank you in advance! Best regards, Youssef
sample.Aligned.sortedByCoord.out.final_fusions.txt