"Infinite Variation"
Posted: Thu Dec 31, 2009 4:40 pm
Kevin, I apologize, you're right, and certainly we did not mean to "highjack" the thread! So I thought I'd start a new thread to say something about the phrase "infinite variation" since it so frequently invoked.
2. The same is true for fingerprints. Putting aside L3D (which by the way, HAS BEEN and IS CURRENTLY being modeled, therefore...means it can be captured and is not "infinite"), but just focusing on L1D and L2D, the variation is NOT infinite. It might be vast and it might be untestably varied, but it's not infinite.
IF it were infinite, I would occassionally see a fingeprint shaped like Nicole Kidman or maybe see the outline of Johnny Depp, maybe even a little Ricky Gervais profile in another. Instead we predictably see common patterns (loops whorls arches) and the ridges predictably flow through these patterns in typical ways. In certain areas of the prints, the ridges behave very characteristically: deltas have lots of short ridges and ridge endings, type lines lots of ridge endings, cores have stacked/multiple enclosures, sometimes mirrored on either side of the rod. In fact, every single clue you've ever learned to "search smart, not hard" means that there is a pattern. And where there is a pattern, there is a loss of randomness.
No doubt these features are highly variable, exhibit extreme characteristics of ability to discriminate various sources...but I think we may need to move away from invoking this term of "infinite variation".
The very fact that we can model and capture L1D L2D and soon/recently L3D, means that this variation can be expressed at some level. And we will only get better at it.
I have often asked colleagues, when the technology is finally here and validated and can express L1D, L2D, and L3D in terms of probabilities, what then will be the excuse for not using this technology. Since that's what we do, use all 3, what reasons are left?
What do you think, Kevin?
1. The analogy to DNA is not quite right. Technically STR DNA methods compare the number of repeating sequences at a site...meaning a "12, 13" is someone with 12 repeating sequences of a certain description (i.e. AGT,AGT,...AGT x12 and AGTx13 on the complementary chromosome. Thus technically, there is no reason someone can't be a "120, 180"...it just doesn't happen. For that site, maybe the rarest someone sees is 30 repeating sequences...but technically 120 could happen...it's just statistically improbable. Thus DNA in this test DOES have infinite variation, but they are not limited by this and can still make statements regarding source attribution.We had a good discussion going on this in another thread a few weeks back-good stuff. I would point out that DNA is working with base pairs (that only go together one way G-T and A-C) in specific sequences on a specific location to make a match. They extrapolate their numbers based on the size of their database and interpret that to the jury....with FP analysis you are dealing with infinite variability between just minutia not including level 3 detail. You can't extrapolate that into a probability to any degree when dealing with latents in my opinion...AFIS does with their search algorithims but it can't hit the print by itself. just sayin
2. The same is true for fingerprints. Putting aside L3D (which by the way, HAS BEEN and IS CURRENTLY being modeled, therefore...means it can be captured and is not "infinite"), but just focusing on L1D and L2D, the variation is NOT infinite. It might be vast and it might be untestably varied, but it's not infinite.
IF it were infinite, I would occassionally see a fingeprint shaped like Nicole Kidman or maybe see the outline of Johnny Depp, maybe even a little Ricky Gervais profile in another. Instead we predictably see common patterns (loops whorls arches) and the ridges predictably flow through these patterns in typical ways. In certain areas of the prints, the ridges behave very characteristically: deltas have lots of short ridges and ridge endings, type lines lots of ridge endings, cores have stacked/multiple enclosures, sometimes mirrored on either side of the rod. In fact, every single clue you've ever learned to "search smart, not hard" means that there is a pattern. And where there is a pattern, there is a loss of randomness.
No doubt these features are highly variable, exhibit extreme characteristics of ability to discriminate various sources...but I think we may need to move away from invoking this term of "infinite variation".
The very fact that we can model and capture L1D L2D and soon/recently L3D, means that this variation can be expressed at some level. And we will only get better at it.
I have often asked colleagues, when the technology is finally here and validated and can express L1D, L2D, and L3D in terms of probabilities, what then will be the excuse for not using this technology. Since that's what we do, use all 3, what reasons are left?
What do you think, Kevin?