Hi all, I am running Bowtie2 to get mapped reads and unmapped reads (--un-conc) from a paired-end experiment.
My command line is like this:
bowtie2 -p 8 --no-unal --un-conc sample1_un.fq -x BDGP6.dna.primary_assembly -U sample1_R1.fastq.gz,sample1_R2.fastq.gz -S sample1.sam
I get a sam file output with content, but the sample1_un.1.fq and sample1_un.2.fq files generated from --un-conc are empty. The output to the screen says 0.67% overall alignment rate so I expect big files in the unmapped reads. The input DNA is human with spike in Drosophila DNA so the alignment rate makes sense.
If anyone could explain what I'm doing wrong that would be great.
Thanks in advance,
T
Try it without
--no-unal
and see if that fixes it.