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TGen Scientists Uncover New Field of Research that could Help Police in
Crime Scene Forensics 



Resolving individuals contributing trace amounts of DNA to highly complex
mixtures using high-density SNP genotyping microarrays 


08-28-2008

PHOENIX, Arizona - August 29, 2008 - A team of investigators led by
scientists at the Translational Genomics Research Institute (TGen) have
found a way to identify possible suspects at crime scenes using only a small
amount of DNA, even if it is mixed with hundreds of other genetic
fingerprints. 

Using genotyping microarrays, the scientists were able to identify an
individuals DNA from within a mix of DNA samples, even if that individual
represented less than 0.1 percent of the total mix, or less than one part
per thousand. They were able to do this even when the mix of DNA included
more than 200 individual DNA samples. 


The results appear today in PLoS Genetics, a peer-reviewed open-access
journal published by the Public Library of Science. 


The discovery could help police investigators better identify possible
suspects, even when dozens of people over time have been at a crime scene.
It also could help reassess previous crime scene evidence, and it could have
other uses in various genetic studies and in statistical analysis. 


"This is a potentially revolutionary advance in the field of forensics,"
said the paper's senior author, Dr. David W. Craig, associate director of
TGen's Neurogenomics Division, which otherwise is charged with finding ways
to treat diseases and conditions of the brain and nervous system. "By
employing the powers of genomic technology, it is now possible to know with
near certainty that a particular individual was at a particular location,
even with only trace amounts of DNA and even if dozens or even hundreds of
others were there, too." 


The researchers analyzed complex mixes of genomic DNA using high-density
Single Nucleotide Polymorphism (SNP) genotyping microarrays. This approach
enabled them to accurately identify individuals from DNA mixes of at least
200 people using less than one in one-thousandth of the total mix.
Theoretically, they showed that individuals could be identified in mixes of
more than 1,000 people. 


Currently, it is difficult for police forensic investigators to detect an
individual if their genomic DNA is less than 10 percent of a mix, or if it
is from a large mix of DNA material. A long-held assumption within the field
of forensic science was that it was not possible to identify individuals
using pooled data - until now. 


According to Commander Brent Vermeer, director of the Phoenix Police
Department crime lab, much DNA evidence is rendered useless because of
contamination, and that to eventually put the TGen theoretical research into
a cost-effective police practice "would be an amazing asset.'' 


A new Arizona law, Senate Bill 1412, passed in June by the Legislature,
requires police agencies to keep DNA evidence in cases of homicide or felony
sexual assault for as long as convicts are in prison or on supervised
release, or at least 55 years in unsolved cases. Some like Phoenix keep it
indefinitely. 


"As technology advances, we need to be prepared to keep evidence that, down
the road, could prove again to be useful," said Vermeer, who heads a bureau
of nearly 130 analysts and crime scene investigators. 


Craig said the findings presented in the paper should foster more scientific
investigation that could lead to cost-effective ways of using the TGen
technology to fight crime. 


"It opens up ideas never considered before," Craig said. 


Dr. Stanley F. Nelson, director of the UCLA site of the National Institute
of Health's Neuroscience Microarray Consortium, said forensics investigators
are "often stymied" because they now search for fewer than 20 DNA markers.
The TGen researchers looked at hundreds of thousands of markers to make
their identifications, he said. 


"It opens up a whole new can of worms of what's possible to do
forensically," said Nelson, professor of Human Genetics and Psychiatry at
UCLA's David Geffen School of Medicine. Nelson contributed to the TGen
paper. 


Nelson said that, using current police methods, DNA processing costs less
than $50, while a similar process for genomic research costs several hundred
dollars. However, with advances in technology, those costs should come down,
he said. 


The TGen study resulted from what Nelson described as "an intellectual
curiosity" by Craig while investigating diseases. Nils Homer, a former TGen
intern who now is working on his doctorate degree in computer science at
UCLA, brought Nelson and Craig together. Homer is the paper's first author. 


"We demonstrate an approach for rapidly and sensitively determining whether
a trace amount... of genomic DNA from an individual is present within a
complex DNA mixture," the paper said. 


# # # 


About TGen
The Translational Genomics Research Institute (TGen) is a non-profit
organization dedicated to conducting groundbreaking research with life
changing results. Research at TGen is focused on helping patients with
diseases such as cancer, neurological disorders and diabetes. TGen is on the
cutting edge of translational research where investigators are able to
unravel the genetic components of common and complex diseases. Working with
collaborators in the scientific and medical communities, TGen believes it
can make a substantial contribution to the efficiency and effectiveness of
the translational process. 







 

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