Hello,

I have several single-end fastq files. Before trimming with Trimmomatic, FASTQC reported TruSeq adapter sequences as possible source of overrepresented sequences. However, after trimming, now FASTQC reports Clontech SMART CDS Primer II A as source of overrepresented sequnces. What should i do about them? Can those sequences cause any negative effects on downstream analysis?

Thanks in advance.

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