Hi,
I am processing a batch of sequencing data, which comes from special library construction technology, and it may contain more adapter sequences than standard library data. I have been informed that the adapter sequences used in library construction are:
> P7_adapter
AGATCGGAAGAGCACACGTCTGAACTCCAGTCAC
> P5_adapter
AGATCGGAAGAGCGTCGTGTAGGGAAAGAGTGT
First, I tried to directly remove these sequences using cutadapt with params -a AGATCGGAAGAGCACACGTCTGAACTCCAGTCAC -A AGATCGGAAGAGCGTCGTGTAGGGAAAGAGTGT, but it was not effective. FastQC shows that there are still a lot of Illumina universal adapters in R2.
Then I tried using shorter adapter sequences -a AGATCGGAAGAG -A AGATCGGAAGAG, and in this case, it worked very well. However, my fastqc report shows that TruSeq Adapter, Index 7 sequences are overrepresented. I'm not clear about the reason for this phenomenon and would like guidance on how to remove these sequences.
fastqc
ngs