samtools sort: failed writing to "/var/tmp/samtools.18.2128.tmp.0000.bam": Inappropriate ioctl for device
and
Fatal error: Exit code 1 ()
It runs for a bit then this pops up, Im very new to using galaxy tools or sequencing.
Created a paired collection from two fastq files and ran fastp on them, and then bwa-mem on the output. Ive deleted the original fastq files to save space.
Tried an older version of bwa-mem and it seems to crash as well
[M::mem_pestat] low and high boundaries for proper pairs: (1, 635)
[M::mem_pestat] analyzing insert size distribution for orientation RF...
[M::mem_pestat] (25, 50, 75) percentile: (49, 86, 128)
[M::mem_pestat] low and high boundaries for computing mean and std.dev: (1, 286)
[M::mem_pestat] mean and std.dev: (84.60, 52.07)
[M::mem_pestat] low and high boundaries for proper pairs: (1, 365)
[M::mem_pestat] analyzing insert size distribution for orientation RR...
[M::mem_pestat] (25, 50, 75) percentile: (110, 150, 204)
[M::mem_pestat] low and high boundaries for computing mean and std.dev: (1, 392)
[M::mem_pestat] mean and std.dev: (159.38, 66.53)
[M::mem_pestat] low and high boundaries for proper pairs: (1, 486)
[M::mem_pestat] skip orientation FF
[M::mem_pestat] skip orientation RF
[M::mem_pestat] skip orientation RR
[E::bgzf_flush] File write failed (wrong size)
[E::bgzf_close] File write failed
[E::bgzf_flush] File write failed (wrong size)
[E::bgzf_flush] File write failed (wrong size)
[E::bgzf_close] File write failed
[E::bgzf_close] File write failed
[E::bgzf_flush] File write failed (wrong size)
[E::bgzf_flush] File write failed (wrong size)