Hi all, i want to perform some analysis on small RNA sequence samples retrieved from the Sequence Read Archive (SRA). since adapter contamination is common in small RNA seuquencing results, its important to clip the adapter from the retrieved fastq file before the downstream analysis. to clip the adapter, i need to know its sequence.
so my question is : how do i know what was the adapter used in the sample preparation?
an example experiment : SRAsmallRNA_experiment