Less than a year back, there was some hype about "generating uniform droplets for bead-based PCR amplification." posted in "In Sequence", June 2008. The idea was that a uniform droplet might affect the quality of the read length on a 454 sequence run. I can't seem to find anything further about it. Has anyone tested this to see if uniform droplets help to obtain longer reads on a titanium run?
Sincerely
Ed Wilcox
Sincerely
Ed Wilcox