Claremont killer trial LIVE: Defence uncovers five examples of DNA contamination in Ciara\'s samples by 2004

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Claremont killer trial LIVE: Defence uncovers five examples of DNA contamination in Ciara's samples by 2004

State seeks to clarify impact of contamination on results

Mr Hollingsworth is re-examining Dr Harbison and asking about which fingernail samples were impacted by the contaminated 'blank' or control samples.

She said AJM41 and AJM46 - which returned the presence of a female DNA profile - were in a batch with a contaminated blank. She said this means the SGM+ results become invalid, however the Y chromosome testing, which detected no male DNA, is still valid. 

The critical exhibit AJM42's blank was blank. 

The AJM42 sample was created in the Pathwest lab in 2001 during a purification process known as Qiagen. 

Dr Harbison has completed her evidence. 

Court has adjourned for morning tea

It will resume at midday. 

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Defence uncovers five examples of contamination within Ciara's samples by 2004

Mr Yovich has now pointed out, of the 35 re-agent blanks, or control samples, the NZ lab received from Pathwest in 2004 - 14 were not tested by ESR, and 21 were. 

Of the 21 tested, four were found to contain female DNA. The purpose of a negative control, is to provide a sample that has no DNA present to ensure the other test results from that batch are accurate. 

Mr Yovich: What, if anything, does that say about the quality of the work at the lab that supplied these blanks?

Dr Harbison: It's not unheard of, although it's not common. 

She said nowadays, of the 50,000 samples that are tested in the NZ lab, "one or two a year" may return a positive result for having been contaminated with DNA from an unrelated source, such as a staff member. 

She said in 2004, the number would likely have been similar, although she could not recall. 

Justice Stephen Hall has asked if it's able to be determined whether the four examples of cross-contamination occurred at Pathwest, when they extracted the samples, or at ESR. 

"[I can't] 100 percent [discount that the contamination occurred in the ESR lab] but ... there was a smaller window of opportunity and the amplification process [we carried out] included a negative control, introduced at that step, and those were clear," Dr Harbison said. 

She said there were more opportunities for the Qiagen extracts to have been contaminated in the Pathwest lab. 

Today, the unrelated DNA could be tracked to the person it came from, however in 2004, this was a manual process, and ESR did not carry out an investigation at the time. 

Defence hones in on potential DNA contamination

Paul YovichCredit:sds

Defence lawyer Paul Yovich has begun his cross-examination of Dr Harbison. 

He is asking about the third allele, found in the AJM41 fingernail sample when tested. 

"All we can tell ... is that there is a suggestion of a second contributor, there's no suggestion that contributor was male because no male DNA was detected, and your testing is sensitive for male DNA," he said. 

He has now asked what the minimum threshold amount of DNA was to return a profile using its SGM+ testing and Y chromosome testing. 

Dr Harbison said for SGM+, a full DNA profile could be obtained by samples with 0.1 nanograms of DNA, and a partial profile could be obtained from even less. 

For the Y chromosome testing she said a full profile could typically be obtained from 0.1 nanograms, and sometimes less than that. 

For reference, 100 DNA cells weigh 0.6 of a nanogram. 

Mr Yovich is now asking Dr Haribon when the NZ lab changed its practices to reduce the risk of contamination following the introduction of more sensitive DNA technologies. 

"As we moved through the 1990s that's definitely the case, by the time we were using the SGM+ testing [in 1997]... our work practices haven't changed significantly since then," she said. 

She said in 1997, a sample would have been handled with disposable, single-use blades and tweezers which were cleaned with ethanol between each use. 

Before 2004, she said scientists switched from wearing cotton lab coats to disposable paper lab coats. She also said tweezers and other lab equipment started to be washed in solution, then ethanol, and then UV treated, between each use. 

She also said by 2004, gloves were single-use only to prevent risk of cross-contamination from one item to another through the gloves. 

NZ forensic scientist resumes giving evidence for second day

Dr SallyAnn Harbison. Credit:Stuff.co.nz

New Zealand forensic scientist, Dr SallyAnn Harbison, has resumed giving her evidence for the second day. 

Prosecutor Bradley Hollingsworth has moved to asking Dr Harbison about some statistics WA Police asked the NZ Institute of Environmental Science and Research to assist with in 2016. 

The statistics related to DNA samples involving Ciara and accused man, Bradley Edwards. 

Mr Edwards was arrested in late December, 2016. 

Ciara's reference profile matched the DNA profile found on Ciara's left index fingernail (AJM41), which had the most DNA present of the four fingernails tested by the lab. 

The DNA testing of this sample revealed 10 loci, all matching Ciara's reference sample. 

One of the 10 loci, that each usually give a result for two alleles, showed a result for an additional third allele. 

"This may be a genuinely mixed profile with DNA from another person in the fingernail sample, it's also possible that this is DNA introduced into the sample during the processing, there is a small chance that sometimes it could be what you would observe with a mutation event, however that is not reflected in the reference loci," Dr Harbison said. 

She confirmed if the third allele came from another person, it was likely a female. 

Ciara's reference profile was also a partial match at her left middle fingernail (AJM42) which had less DNA present, and was more degraded. 

Dr Harbison said all the available locus (6/10) matched Ciara's DNA profile. 

Of the causes of degrading of DNA, Dr Haribson said: 

"Prolonged exposure to the environment is one factor, for example sun or water, if a sample is dry and kept out of direct sunlight it will last for many years, but a sample that's been outside or in a humid environment for example, the DNA will degrade quite quickly.”

Recap: What was discovered under Ciara's fingernails and when

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'NZ DNA testing in 2004 proves samples weren't contaminated in Pathwest lab': Prosecutor

State prosecutor Carmel Barbagallo Credit:AAP

During her trial opening address, prosecutor Carmel Barbagallo explained why the 2004/2005 testing carried out at the NZ Institute of Environmental Science and Research (ESR) was important in proving the fingernail samples were not contaminated.  

"The state relies on these DNA results obtained by both Pathwest and ESR from 1997 to 2005 in part to demonstrate that the DNA extracts prepared from the fingernail samples originally and the DNA profiling subsequently undertaken with these extracts, particularly by Pathwest are reliable, produce results which are entirely consistent with Ciara Glennon being the person from whose fingers the nail clippings were cut from, and that the processes employed were otherwise free from any evidence of contamination, whether specific to the exhibit or extracts being tested, or to the process within the laboratory generally," she said. 

"The ESR results are also particularly instructive, in that at no time did ESRs tests confirm the presence of male DNA on any of the fingernail exhibits, both in extracts prepared by Pathwest in 1997 and upgraded in 2001 and in the extracts prepared by ESR from the same exhibits in 2004.

"Further, given that for AJM41 and 42, ESR were able to obtain full or close to full single source SGM Plus profiles from the fingernail samples provided, these results are not only demonstrative of the absence of any evidence of contamination [they are] also capable of supporting the validity and accuracy of the DNA profiles developed by FSS [Forensic Science Service lab in the UK] using the same kit, albeit through low copy number techniques [during its combined testing of AJM40 and AJM42 in 2008]."

Day 40 of trial to start at 10am

Ciara Glennon

Welcome to WAtoday's live coverage of day 40 of the Claremont serial killer trial in the Supreme Court of Western Australia. 

Today, Dr SallyAnn Harbison, a DNA expert from New Zealand, will continue to give evidence about how some of Ciara's fingernails were sent across the ditch in 2004 to undergo Y chromosome testing in an attempt to draw out her killer's identity.

The fingernails sent were: AJM41, AJM42, AJM46, AJM49 and AJM50. 

The testing only revealed one DNA profile, being Ciara's. 

AJM42, Ciara's left middle fingernail, is one of the state's critical pieces of evidence. It alleges once combined with AJM40 (Ciara's left, torn thumbnail), and tested in 2008 in the UK, it revealed a mixed DNA profile consistent with Ciara and accused man, Bradley Edwards.

It's alleged Mr Edwards' DNA got under Ciara's fingernail when she scratched him in a fight for her life. 

Prosecutors claim the yellow top container which housed Ciara's torn left thumbnail was only opened once - in 2008, and have called the sample "pristine". 

AJM42's yellow top container was opened in 1997 and 2004. After the New Zealand testing, which found the sample only contained Ciara's DNA profile, the sample container was not opened again until 2008 in the UK. 

Mr Edwards' defence team is arguing Ciara's fingernail samples - at some stage while in the Pathwest lab - became contaminated with the accused's DNA profile, which was housed in the lab within exhibits relating to the rape of a 17-year-old girl in Claremont in 1995. 

Mr Edwards' has pleaded not guilty to the murders of Sarah Spiers, Jane Rimmer and Ciara Glennon. 

For a full catalogue of WAtoday's coverage of the trial, click here

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