Larry Moran has an excellent discussion of the organization of rRNA genes in the human genome. It's an old post, but a good one.
If you're involved in RNA-Seq, you should read it. Dr. Moran's discussion makes it clear why it is necessary to map reads to a synthetic rRNA-ome before doing full-genome alignment -- if you want to accurately count, or filter out, rRNA reads (which can predominate in RNA-seq datasets).
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