rRNA Contamination in the RNA-seq library
I have to run CIRI on several fq files for the identification of circular RNA but realize that there is a small percentage of rRNA contaminants within them. know We did not remove the contamination before library construction earlier as protocol. Now that I have run hisat2 on files and CIRI on .sam for circular RNA identification. Is there a way to remove the contaminants? Thanks!
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