Some potential collaborators are interested in designing PCR primers within a few kb of ribosomal DNA repeats in the human genome. My limited understanding of these ribosomal DNA repeats is that they are currently in gaps in the human genome on chromosomes 13, 14, 15, 21, and 22. Does anyone have experience with working with these troublesome regions or sequences? In short, what is sought is unique sequence flanking one or more of the rDNA repeats.