If that is enough, then what do we use 13 for? It is not enough.
I'm not sure why 13 loci is the standard for the US. The British system uses 10 loci. In the US, 9 or 10 loci is enough to be entered into CODIS. But the fact is that 10 is enough to be virtually certain. The odds of two pieces of DNA evidence from the same crime scene to have the same 10 loci, and no differing loci is absolutely astronomical.
There are people that are saying the DNA under her nails is also a match and that DNA has 3 markers. I don't think so. The fact that there is not a total of 13 markers leads it open to a false positive. It is not foolproof by any stretch of the imagination including Lacy's and Ramseys.
3 markers is not enough. I agree. But 10 is.
I am not deriding your paper. I am at work and you pass on a document with print that is so small it is somewhat comical. If you want to cut and paste some of the essential info, I would and know others would appreciate it. Give me a break here. Pretend your on tv and have a certain amount of time - are you going to give the interviewer th epaper and tell her to read it.
The paper is not small on my computer. The text is actually pretty big. I have the PDF version, and it is the version that I thought I linked to.
Here are some the essential finding of the study,
"The STR results regarding primary and secondary DNA transfer
were identical to those for AmpliType PM 1 DQA1. Primary
transfer was observed in some cases using Profiler Plus and
COfiler. As with the dot-based systems, sample degradation in addition
to low DNA yield appeared to be significant factors. Locus
and allele dropout were particularly problematic for the larger amplicons.
With respect to secondary transfer, peaks above background
(15–20 RFU) from the second individual were not detected
for most STR amplifications. On occasion, minor peaks (below 75
RFU) from the second individual were observed. However, in
these instances, allele dropout was routine. The complete secondary
profile was never detected, even if the data were analyzed
in the 50–75 RFU range. It should also be noted that, generally,
amplification would not be attempted on many of the experimental
samples we tested since the manufacturer recommends using a
minimum of 250 pg (35 cells) of DNA template for PCR."
and
"Our data indicate that the primary transfer of DNA by handling
is possible, but detecting an interpretable genotype is not assured.
Secondary transfer was not observed under our experimental conditions.
Therefore, our data do not support the inference that the interpretation
of DNA profiles from case samples could be compromised
by secondary transfer."