'problem 1' : using a single 10mer (random) primer i get pcr products from
200bp to 3kb with no template dna....the question is how does a single 10mer
primer create sufficient secondary structures for such amplifications?
has anyone else seen this?....some of these bands ARE seen in rxns using
'problem' 2: whats the program of choice when it comes to analyzing rapd pcr
products to create phylogeny trees etc...and how can i get access to them?