I have ~100 Bissulfite-Seq fastq files and ~100 RNA-Seq fastq files representing many samples. All of the seq files were produced by Illumina tech.
I want to pre-process the fastq files by removing bad-quality base calls and adapters. The problem is that I do not know any adapter used for any of these files.
My question is: Is there any default adapters for Illumina Seq? I found in the documentation of Trim Galore that the default adapter is (AGATCGGAAGAGC). Shall i use it?
I want to pre-process the fastq files by removing bad-quality base calls and adapters. The problem is that I do not know any adapter used for any of these files.
My question is: Is there any default adapters for Illumina Seq? I found in the documentation of Trim Galore that the default adapter is (AGATCGGAAGAGC). Shall i use it?
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