just for fun, the limiting factor as far as a lab setup goes, is probably handling all the samples as they come in the lab and keeping track of them, not actually processing them. producer A has 1 sample, producer B has 37, producer C has 1240 and so on. labs are set up to do things in increments of 8, 12, 24, 96, 384. with automation, it's relatively easy to process the samples, even if they are run on agarose gels as TH and PHA are. believe me, they are doing it cheaply for the non lab portion of work they have to do, not to mention the cost of finding the defect. could they do it cheaper? sure, but the best way to make it cheaper is if you use carrier genetics and feel they have a merit, convert them to free status in a couple of generations. then the test won't be needed any more unless someone is interested in the odd cross of using older genetics. then the test will be a sort of novelty, yeah in the dark ages TH and PHA was a problem, now we only have to deal with arthritis, mealy feet, monkey mouth, the many sources of dwarfism etc. what's great is that the means to finding these genes is getting easier, and even easier if the parentage is correct.
as far as PHA genetics goes, is there a bull with the spring of rib of ice pick?