Hello,
My file is Clean fastq file from Illumina HiSeq 3000 with 2X100 cycles run.
When ran fastqc, they have over-represented sequence of adaptor and primer.
What can I do?
Thanks in advance!
Yue Li
My file is Clean fastq file from Illumina HiSeq 3000 with 2X100 cycles run.
When ran fastqc, they have over-represented sequence of adaptor and primer.
What can I do?
Thanks in advance!
Yue Li