"The probability of a coincidental match means the chance that Mr. Puckett's DNA would match (and no other DNA in the database would) if he were not the killer and if he were unrelated to the killer.I'm not sure what exactly the criticism is. It's true that the probability of a coincidental match is 1.1 million for that specific person is 1.1 million, and the probably of any coincidental match is one in three.
This definition refers to the probability of the DNA evidence given the hypothesis of coincidence. Again, neither 1 in 1.1 million nor 1 in 3 expresses this value, but 1 in 1.1 million is a far closer estimate than is 1 in 3. (...)
Definition 2. The probability of a coincidental match means the chance that Mr. Puckett's DNA would match (and no other DNA in the database would) if he were not the killer and if he were unrelated to the killer.That would be nice, but according to the linked article that didn't happen, in fact, they found 9 other matches, or possibly 122. Remember with this 'half marker' or whatever there was additional possible sequences.
...
This definition refers to the probability of the DNA evidence given the hypothesis of coincidence. Again, neither 1 in 1.1 million nor 1 in 3 expresses this value, but 1 in 1.1 million is a far closer estimate than is 1 in 3.
Definition 3. The probability of a coincidental match means the chance that one or more DNA profiles in the database would match if no one in the database is the killer.Exactly. 1 in 3. As far as I can tell, the "definition 2" provided is totally spurious.
This definition refers to the probability of one or more hits in the database given that the database is innocent. This probability is approximately 1 in 3.
That would be nice, but according to the linked article that didn't happen, in fact, they found 9 other matches, or possibly 122. Remember with this 'half marker' or whatever there was additional possible sequences.That's not what the article said at all. The article said that when the evidence from the Sylvester case was run against the California DNA database, there was "a" match -- Puckett.
Simple Sequence Length Polymorphisms (SSLPs) are used as genetic markers with Polymerase Chain Reaction (PCR). An SSLP is a type of polymorphism: a difference in DNA sequence amongst individuals. SSLPs are repeated sequences over varying base lengths in intergenic regions of Deoxyribonucleic Acid (DNA). Variance in the length of SSLPs can be used to understand genetic variance between two individuals in a certain species.(wow, with no context and a skilled lawyer I can see how the involved sciences can be made to resemble reading tea leaves {or conversely to be venerated as flawless and infallible as determinants of guilt [as pointed out above, the ultimate reality of a scenario must involve Motive-Means-Opportunity with full explanations] to allow a logically sound determination of guilt beyond all reasonable doubt.} These Genetics sciences are actually extremely interesting to read more of the science, and realize the vast variety of scales of reference which can be examined through DNA, from an individuals history, to familial relations, ancestry, and even markers from specific events can signify where a particular ancient distant relative was at some point in time.)
the term restriction fragment length polymorphism, or RFLP, (commonly pronounced “rif-lip”) refers to a difference between two or more samples of homologous DNA molecules arising from differing locations of restriction sites, and to a related laboratory technique by which these segments can be distinguished. In RFLP analysis the DNA sample is broken into pieces (digested) by restriction enzymes and the resulting restriction fragments are separated according to their lengths by gel electrophoresis.
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posted by homunculus at 1:47 PM on March 6, 2010