McHrnozni, I can assure you I can talk tech on these matters far better than you.
A couple of problems here. Number one: you can't verify anything without raw data.
You seemed to misunderstood what I was saying I didn't need, I wasn't talking about the chromatograph traces. I meant there was no need to release the actual genotypes of each loci, since this would have privacy implications.
Methodology was either STR or VNTR
http://en.wikipedia.org/wiki/Short_tandem_repeat
http://en.wikipedia.org/wiki/VNTR
Either would be suitable. VNTR can probably be made on any aircraft carrier with only a small amount of quite inexpensive equipment.
Well here is your first howler as STR are is just a subset of VNTR. STR is the new terminology for microsatellite. In terms of genotyping efficiency the differences are trivial and I would expect that the FBI would just be using standard commercial kits that would mostly contain STR loci, although perhaps they might include SSRs. There is no difference in equipment or reagents, the only difference would be the primer chosen.
While the equipment is not madly expensive (ie a few hundred thousands), it is not normally or ever deployed in a mobile deployment (although there are some technologies in prototype that could be - however firms involved have denied any involvement saying it is too early to be testing in the field and certainly not in such an operation).
One of the issues that makes an aircraft deployment unlikely is the fact that capillary electrophoresis is (or used to be anyway) quite sensitive to level and vibration. Choose a selection of links from the ABI site to satisfy your curiosity on this matter
http://www.google.com.au/search?cli...equencer+vibrations&pbx=1&fp=6ed37e06fcb306d6
I am not sure how much buffeting or vibration an aircraft carrier today gets and if that would interfer. In any case I am confident, given the long period since the Carl Vinson has been state side, they did not fly an ABI 3000 series out there.
Both could be done in 12 hours.
Probably a bit less, but the samples have to reach a genotyping facility first. If it wasn't Bagram it would almost certainly be the US. Which means the results were annouced before the test were completed. In fact a successful DNA match was announced much sooner than 12 hours from leaving Abbottabad.
I suspect you know now exactly as much as you did before you asked.
Yes, but I do appreciate your hamfisted attempt at trolling.
To show the sort of detail in regards to genotyping I would like to know what kit was used.
Eg. an ABI Identifiler kit using the following markers
15 STR loci (CSF1P0, D2S1338, D3S1358, D5S818, D7S820, D8S1179, D13S317, D16S539, D18S51, D19S433, D21S11, FGA, TH01, TPOX, vWA)
or a Promega PowerPlex 16 kit using
sixteen loci (fifteen STR loci and Amelogenin): Penta E, D18S51, D21S11, TH01, D3S1358, FGA, TPOX, D8S1179, vWA, Amelogenin, Penta D, CSF1PO, D16S539, D7S820, D13S317 and D5S818
Then you would want to know what relatives and the degree of relatedness (names not needed) and the number of markers shared.
However, in fact all I want is the head of a lab to speak up and say they genotyped it, when and where, and they stake their credibility on the results.
If DoD really did set up a genotyping facility on the Carl Vinson then I would like them to come out and say it. It would be the first time a genotyping facility would have be deployed in such a way for a one of genotyping.