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8.9 years ago
dgtiezzi
▴
10
Using the FASTQC I have those overrepresented adapters (RNAseq data):
GATCGGAAGAGCGGTTCAGCAGGAATGCCGAGACCGATATCGTATGCCGT
GATCGGAAGAGCGGTTCAGCAGGAATGCCGAGACCGATCTCGTATGCCGT
GATCGGAAGAGCGGTTCAGCAGGAATGCCGAGATCGGAAGAGCGGTTCAG
How is the best approach to trim them out using cutadapt? Copy and paste the sequences after -a
? Can I give multiple adapters at once?
Question: would cutadapt -a AdapterSeq1 -a AdapterSeq2 -a AdapterSeq3 -o output.fastq input.fastq work?
It will work, but Cutadapt will only trim the adapter with the best match. Please refer to the section "Trimming more than one adapter from each read" in the same documentation as Juke-34 has mentioned. Excerpt from the documentation,