We need to be able to remove rRNA-derived library molecules from PCR amplified mRNAseq library, rather than removing the rRNA itself during the earlier steps of library construction. We don't need to remove every single rRNA-derived molecule, but would be very happy if we could, say, cut the number of rRNA reads by 75%.
Does anyone know how, other than by DSN?
Thanks!
eab
Does anyone know how, other than by DSN?
Thanks!
eab
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