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Old 04-20-2018, 01:22 PM   #1
yueli
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Location: china

Join Date: May 2013
Posts: 53
Default adaptor and primer from fastqc

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
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