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Which end of the reads are you going to trim in most FASTQ files?
Which module in the FastQC report will show you whether you need to trim bases with low quality?
Next to trimming low quality bases from the ends of the reads, you can also remove complete reads with low average quality.
Which modules in the FastQC report show whether you have to filter low quality reads from the FASTQ file? There are 2 correct answers.
Very often you also need to remove adapter contamination. Which module in the FastQC report shows whether you have to filter adapter sequences?