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[1999] VSCA 164
Court of Appeal (Vic)
1999-10-07
PHILLIPS, C.J., ORMISTON and CALLAWAY, JJ.A.
Original judgment source is linked above.
"1. The evidence relating to the deoxyribonucleic acid ('DNA') analysis presented by Dr. Gutowski was incomprehensible or alternatively could not be understood by the jury.
2. No evidence or sufficient evidence was presented to establish Dr. Gutowski's knowledge or expertise in the subject of statistical analysis to qualify him to express statistical conclusions.
3. The evidence relating to the statistical analysis presented by Dr. Gutowski was incomprehensible or alternatively could not be understood by the jury.
4. The directions to the jury on the subjects of the DNA evidence and the statistical analysis were inadequate because:
(a) the jury should have been directed not to approach the issue of chance upon any strictly mathematical basis; and
(b) the directions were constructed in such a way as to permit the jury to accept the conclusions expressed by the experts and to avoid proper analysis."
"DNA is the abbreviation for deoxyribonucleic acid which is contained in the nucleus of cells in chromosomes in the human body. It is described as the building block of life and is the material, in most cells, that is the code for each of a person's characteristics, eg colour of hair and eyes, and is unique to each person except in the case of identical twins. DNA is consistent throughout the body and so, in the case of a male, the DNA in his blood is the same as in his semen. Each person has 23 pairs of chromosomes, one of each is inherited from each parent. The DNA in each chromosome has two strands which are held together by pairing mechanisms which are pairs of the bases. There are four different bases called A G T C [adenine, guanine, thymine and cytosine] which behave in a certain way; A always pairs up with T and G with C. There are about 3 billion base pairs along the strands of DNA and their sequence is responsible for the characteristics of a person. Almost 3 million sites vary from person to person.
The polymerase chain reaction (PCR) is a technique which amplifies or copies a small region of DNA millions of times. Only a small number of the bases are looked at by the PCR method. By using this method the type of DNA chosen is very variable from person to person. Once the chosen region is copied up there is produced two DNA fragments from each strand, one from each parent. One is longer than the other and they are separated. The PCR method provides a way of measuring the length of these two fragments which are known as alleles and their size is described by numbers. The two alleles together provide the genotype of a person."
Dr. Gutowski used methods based on PCR which, he said, had superseded restrictive fragment length polymorphism (RFLP) analysis: cf. The People v. Barney 10 Cal.Rptr. 2d 731 (1992) at 735.
"It is sufficient to state that the PCR test focuses upon small areas situated on different chromosomes of the long DNA molecule. These discrete loci are identified by the designations HLADQA1, D1S80 and HUMTHO1. Each locus has different forms or alleles of DNA. For example, in the case of HLADQA1 there are six different alleles, whilst the D1S80 [has] over 25 alleles. Since one allele is contributed by each parent there are varying numbers of possible combinations to be discerned in each site. For example, in the case of HLADQA1 there are 21 different combinations of the six alleles possible, whilst with D1S80 the combination will certainly be in excess of 100. Moreover, some alleles are more commonly to be found than others.
The significance of the matching allele combinations in the DNA in the suspect's blood and blood found at the crime scene, or upon items which may be associated with the commission of the crime, will depend upon the rarity or uniqueness of such combination within the general population. Possible frequencies of the combination of alleles in the general population are determined by reference to databases kept by the Forensic Science Laboratory in relation to each specific test.
In order to provide a reliable guide to such frequency in the general community, the databases from which such extrapolation is made must be representative of the general community, and the community from which the samples constituting each database is drawn must itself be in Hardy-Weinberg equilibrium (that is the population must effectively be a randomly mating one).
When recourse is had to the relevant database the results of each individual test may be statistically analysed to provide a population frequency for the combination of alleles revealed. Moreover, assuming the independence of each test (that is a lack of any significant statistical relationship between the results obtained from tests performed at each discrete locus) it is legitimate to utilize the product rule (that is the multiplication of the figure for population frequency at each locus) to obtain an overall figure for population frequency.
Again, assuming statistical independence, it is possible to include in such multiplication exercise the results obtained using different systems including, for example, the Gc protein test."
"Where a number of blood tests - each of them operating differently from or independently of the others - have established a match between the suspect and the offender (in the sense that they have not excluded the suspect as such), the inference is that the greater the number of such tests the less the chances are that the suspect is not the offender. Very little more could be gleaned from such matches alone. The significance of those matches becomes far greater where it is possible to calculate the probability of the match having occurred by chance or coincidence. Databases have been built up which are said to demonstrate the probability that another person would share the particular blood type or would match the DNA of the suspect at a particular genetic marker. The greater the number of such matches the greater the probability, so that the statistics are calculated by multiplying the probabilities for each match."
The same point was made by James, J., with whom Wood, C.J. at C.L. agreed, in R. v. Pantoja [No. 2] (unreported, New South Wales Court of Criminal Appeal, 5th November 1998) at 37. Without careful examination, such evidence may appear to be more probative than it is: see R. v. Pantoja [No. 1] at 561-562 and R. v. Humphrey [1999] SASC 67; (1999) 72 S.A.S.R. 558 at 567-568.
"He will properly explain to the jury the nature of the match ('the matching DNA characteristics') between the DNA in the crime stain and the DNA in the blood sample taken from the defendant. He will properly, on the basis of empirical statistical data, give the jury the random occurrence ratio - the frequency with which the matching DNA characteristics are likely to be found in the population at large. Provided that he has the necessary data, and the statistical expertise, it may be appropriate for him then to say how many people with the matching characteristics are likely to be found in the United Kingdom - or perhaps in a more limited relevant sub-group, such as, for instance, the caucasian, sexually active males in the Manchester area."
Subject to the concern as to confidence limits expressed in the next two paragraphs, I do not think that the evidence summarized in [18] travelled outside those limits. It is uncontroversial that independent frequencies may be multiplied.
"So if you've got a database of more than 200, you can automatically apply that to the Victorian population, can you, without the use of confidence limits?---Well, if it's a Victorian database, yes.
Can you tell me why that's a valid thing to do, yourself?---Well, it has to stop somewhere. Obviously if you have say 10 or 15 different varieties of genotype that you can - that you can have, and you have a database of 10 or 15, then you're - the sort of predictions for the frequency in the general population are not going to be terribly accurate. If you have a database of 100,000 and 15 different varieties, then your predictions for the general population are going to be very accurate. Somewhere in between, one starts getting confidence that the predictions are not going to be too far wrong, and that's at around 200.
Why do you pick that figure?---Well, because you can - I've seen papers that look at the maths of this, and at around that figure with around the sort of number of alleles that we're looking at, you start to give reasonably accurate predictions.
In re-examination the figure 200 was said to be an arbitrary convention, which was ascribed to a "relatively august body" made up of "senior managers and scientists" of the International Society for Forensic Haemogenetics.
R
Noll [1999] VSCA 164