I wish to align single end fastq sample using "Map with BWA" tool. The reads were trimmed several times with "Trim Galore" to remove specific adaptor sequences. The reads are 20-50 bp long. I'm using default parameters, except for the read group setting.
But the run quickly fails at start giving the following error:
Fatal error: Exit code 1 ()
[bwa_aln] 17bp reads: max_diff = 2
[bwa_aln] 38bp reads: max_diff = 3
[bwa_aln] 64bp reads: max_diff = 4
[bwa_aln] 93bp reads: max_diff = 5
[bwa_aln] 124bp reads: max_diff = 6
[bwa_aln] 157bp reads: max_diff = 7
[bwa_aln] 190b
Why is this happening?