I am learning to interpret fastQC reports. I combined all the fastq files for R1 and R2 and ran fastQC on them separately. The rest of the summary look good except the duplication levels and Kmer content. For both R1 and R2, there is a slight increase of duplication levels after 10 (I know this is kind of to be expected). What bothers me is the overall high kmer content (above 70%) across all positions in read. I do not have any explanation for it, except that it looks like a systematic error. Is there anything I could do (trimming, filtering, etc.) about it or should I just leave it like that?
Thank you very much!
Thank you very much!
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