Hi I am looking to align some human short read WGS data with BWA-MEM prior to variant calling. I have 62 samples, each has 8 pairs of fastqs (992 fastqs total). I ran fastqc/multiqc on all of them and got this result from multiqc:
For comparison here is an individual fastqc:
Spot checking a handful of individual fastqc reports it seems the flat universal adapter line hovering around 2ish percent and that poly a line creeping up over the length of the read is pretty typical, does this require trimming prior to alignment?
According to this the threshold for warning is 5% and failure is 10%, but just wondering what the general practice is
Thanks!