Hello,
Based on FastQC result, I have two overrepresented sequence. One is my TruSeq Adapter sequence and another seems like a contaminated sequence (below) AAGCAGTGGTATCAACGCAGAGTACTTTTTTTTTTTTTTTTTTTTTTTTTT
I would like to remove/trim this contaminated sequence from my fastq file before mapping, but I don't know how to do it. I heard that this can be done with fastq-grep but not sure how to use grep tool to remove the contaminated sequence.
Thank you for your help in advance.
If you could give me detailed explanation (I am new to usegalaxy!) I would appreciate it so much!