Hello all,
I am processing the original ATAC-seq dataset from Buenrostro et al. 2013. After removing the adapters with cutadapt, where I set a minimum fragment size of 20, and mapping, I filter all the reads shorter than 40 bp to avoid those that only contain adapter. Surprisingly, in the insert size plot, I still see a tiny fraction of very short reads. How is this possible? Is this normal?
Thanks in advance
1 answer
It is probably reads from the mitochondrial genome that are so chopped down and overdigested that you get these small fragments, or some weirdness from the aligner. I say it in that sloppy fashion because it is so few reads that it essentially does not matter. The plot overall looks perfectly normal for this type of experiment, so carry on.
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