Hi all,
I have a Illumina small RNA-seq dataset. I want to know if it is possible to distinguish between a genuine small RNA and a degraded messenger RNA fragment?
The dataset has already been compared to all known small RNA databases. I thought that the percentage of reads which align to exons of known genes might give an idea. Any other ideas/thoughts much appreciated!
I have a Illumina small RNA-seq dataset. I want to know if it is possible to distinguish between a genuine small RNA and a degraded messenger RNA fragment?
The dataset has already been compared to all known small RNA databases. I thought that the percentage of reads which align to exons of known genes might give an idea. Any other ideas/thoughts much appreciated!
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