I'm fairly new around here so I really appreciate all your help! I am trying to concatenate fastq files corresponding to the same samples but ran in different lanes (each end separately), so that I can proceed to trim barcodes. My problem is that I get this error when trying to concatenate. There should be plenty of space left.
Thanks so much!
The Galaxy framework encountered the following error while attempting to run the tool:
Traceback (most recent call last): File "/galaxy-repl/instances/main/server/lib/galaxy/jobs/runners/drmaa.py", line 150, in queue_job self.write_executable_script( ajs.job_file, script ) File "/galaxy-repl/instances/main/server/lib/galaxy/jobs/runners/__init__.py", line 316, in write_executable_script f.write( contents ) IOError: [Errno 28] No space left on device
Tool execution generated the following error message:
failure preparing job script