I've asked for months that some of the people here that are experts get together and write a guide for use in court.
I wish that Planigale, Diocletus, Kaosium, and Chris (use little common words) would write a paper on this case focusing on just three or four pieces of evidence and some basic mistakes in the lab.
I would describe a proper LCN lab, compare it to the Rome lab and explain how easy LCN is to spread by mere touch. IIRC the NY lab used for one of the first LCN used in court and how it was set up, tested and how long that took.
It is important for people to understand that LCN isn't the same as regular DNA in that it can't be seen first. Whereas anyone can understand that if semen, blood or saliva is found in a suspicious location identifying its owner is powerful evidence, finding a microscopic particle of DNA isn't necessarily part of any crime.
So an over view of DNA and LCN. An overview of procedure and protocol in all aspects of collection, transport and testing (storage).
An explanation of how forensic DNA has developed and the value of it in crime work as well as the dangers.
Then go into some detail (footnotes for scientists) of what was wrong with the specific pieces of evidence in this case and showing pieces that were done correctly.
If I forgot an expert it was not intentional.
Thanks for pointing me to this. I'll take a longer look. I once did a PCR training course but this is not my area of expertise. The thing I have been suspicious about is the negative controls for when the RT qtPCR was out of action and the knife was run having got an undetectable from the Qubit.
When the RT qtPCR was in action I have no problems with not typing the negative controls when a count of 50 was returned indicating no detectable DNA so long as no samples with a count of 50 were typed.
The problem arises when the knife was run. Assuming the negative controls returned 'undetectable' on the Qubit one had to decide whether no samples with an 'undetectable' would be further processed. If you decided to process samples with undetectable then you needed to process the negative controls in the same way. My guess is this never happened. So although there were negative controls, and they have returned an 'undetectable', this was not an adequate control process because the sensitivity of the Qubit was not sufficient to detect low level contamination, exactly what might explain the DNA of MK on the blade. The suppression of the typing results is exactly what one would have expected if this happened. I do not blame Stefanoni, the obvious thing was not to type the negative controls with undetectable DNA. The unclear thing is why she processed a sample with undetectable DNA, once she did that she was obligated to do the same for the negative controls, a slip but not I think deliberate. She probably never realised the problem until the defence insisted on the controls. So she was able to stand up and say the negative controls were negative (true), but using an insensitive assay and not treating them the same as the samples invalidates the controls.
I may be wrong, she may have put the negative controls through for typing, in which case why not provide the results, unless of course they showed DNA, even then one could make an argument that as long as they were not showing alleles that might match MK it is irrelevant to the result on the blade. I am very resistant to the idea that Stefanoni deliberately concealed exculpatory results; others may have a different view and think this is a more likely explanation.
When one is working in a lab with serial samples, and there is a sample you decide not to process, let us say in this instance a negative control you decide not to put through for typing, you may leave an empty well. The reason for doing this is variable, but if you are putting multiple samples in to an e.g. 8x8 block you know that sample 8,16,24 are at the end of a row and it is a check that you have not put two samples into the same well. So there may be an innocent explanation for there being some gaps e.g. leaving the wells empty for samples with too low a result that you decide not to process. But then one would just say no sample processed or something similar.