DNA fingerprinting enters 21st Century.
DNA testing (Technology application)
Forensic sciences (Technology application)
|Publication:||Name: The Forensic Examiner Publisher: American College of Forensic Examiners Audience: Professional Format: Magazine/Journal Subject: Health; Law; Science and technology Copyright: COPYRIGHT 2012 American College of Forensic Examiners ISSN: 1084-5569|
|Issue:||Date: Fall, 2012 Source Volume: 21 Source Issue: 3|
|Topic:||Computer Subject: Technology application|
|Geographic:||Geographic Scope: United States Geographic Code: 1USA United States|
SCIENCEDAILY (APR, 27, 2012)--AS ANY CRIME SHOW BUFF CAN TELL YOU,
DNA EVIDENCE IDENTIFIES A VICTIM'S REMAINS, FINGERS THE GUILTY, AND
SETS THE INNOCENT FREE. BUT IN REALITY, THE PROCESSING OF FORENSIC DNA
EVIDENCE TAKES MUCH LONGER THAN A 60-MINUTE PRIMETIME SLOT.
To create a victim or perpetrator's DNA profile, the U.S. Federal Bureau of Investigation (FBI) scans a DNA sample for at least 13 short tandem repeats (STRs). STRs are collections of repeated two to six nucleotide-long sequences, such as CTGCTGCTG, which are scattered around the genome. Because the number of repeats in STRs can mutate quickly, each person's set of these genetic markers is different from every other person's, making STRs ideal for creating a unique DNA fingerprint.
Now Whitehead Institute researchers have pulled STR identification into the 21st Century by creating IobSTR, a three-step system that accurately and simultaneously profiles more than100,000 STRs from a human genome sequence in one day--a feat that previous systems could never complete. The IobSTR algorithm is described in the May issue of Genome Research.
"IobSTR found that in one human genome, 55% of the STRs are polymorphic, they showed some difference, which is very surprising," says Whitehead Fellow Yaniv Erlich. "Usually DNA's polymorphism rate is very low because most DNA is identical between two people. With this tool, we provide access to tens of thousands of quickly changing markers that you couldn't get before, and those can be used in medical genetics, population genetics, and forensics."
To create a DNA fingerprint, IobSTR first scans an entire genome to identify all STRs and what nucleotide pattern is repeated within those stretches of DNA. Then, IobSTR notes the non-repeating sequences flanking either end of the STRs. These sequences anchor each STR's location within the genome and determine the number of repeats at the STRs. Finally, IobSTR removes any "noise" to produce an accurate description of the STRs' configuration.
According to Melissa Gymrek, who is the first author of the Genome Research paper, IobSTR's ability to accurately and efficiently describe thousands of STRs in one genome has opened up many new research opportunities.
"The first and simple next step is to characterize the amount of STR variation in individuals and populations" says Gymrek, who was an undergraduate researcher in Erlich's lab when she worked on IobSTR. "This will provide knowledge of the normal range of STR alleles at each locus, which will be useful in medical genetics studies that would like to determine if a given allele is normal or likely to be pathogenic. Another direction we are looking at is to look at STRs in case/control studies to look for STRs associated with disease. The list goes on, but these are some of the first questions we're looking to tackle."
* This story has been cut from its original form.
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