Only one-tenth of a single percent of DNA (about 3 million bases) differs from one person to the next. Scientists can use these variable regions to generate a DNA profile of an individual, using samples from blood, bone, hair, and other body tissues and products.
In criminal cases, this generally involves obtaining samples from crime-scene evidence and a suspect, extracting the DNA, and analyzing it for the presence of a set of specific DNA regions (markers).
Scientists find the markers in a DNA sample by designing small pieces of DNA (probes) that will each seek out and bind to a complementary DNA sequence in the sample. A series of probes bound to a DNA sample creates a distinctive pattern for an individual. Forensic scientists compare these DNA profiles to determine whether the suspect's sample matches the evidence sample. A marker by itself usually is not unique to an individual; if, however, two DNA samples are alike at four or five regions, odds are great that the samples are from the same person.
If the sample profiles don't match, the person did not contribute the DNA at the crime scene.
If the patterns match, the suspect may have contributed the evidence sample. While there is a chance that someone else has the same DNA profile for a particular probe set, the odds are exceedingly slim. The question is, How small do the odds have to be when conviction of the guilty or acquittal of the innocent lies in the balance? Many judges consider this a matter for a jury to take into consideration along with other evidence in the case. Experts point out that using DNA forensic technology is far superior to eyewitness accounts, where the odds for correct identification are about 50:50.
The more probes used in DNA analysis, the greater the odds for a unique pattern and against a coincidental match, but each additional probe adds greatly to the time and expense of testing. Four to six probes are recommended. Testing with several more probes will become routine, observed John Hicks (Alabama State Department of Forensic Services). He predicted that DNA chip technology (in which thousands of short DNA sequences are embedded in a tiny chip) will enable much more rapid, inexpensive analyses using many more probes and raising the odds against coincidental matches.
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Sunday, June 6, 2010
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- How Do We Inherit Our Biological Characteristics
- How are GM foods labeled?
- How are GM foods regulated and what is the govern...
- What are some of the criticisms against GM foods?
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- What are some of the advantages of GM foods?
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- Reading Chapters In The Genome
- DNA Is Like A Library Of Instructions
- Reading the Sequences
- Unzipping DNA
- The DNA Sequence
- Inheritance
- Tracing Similarities And Differences In Our DNA
- Where Is DNA Found?
- Understanding Gene Testing
- Ethical, Legal, and Social Concerns about DNA Data...
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- How is DNA typing done?
- Is DNA effective in identifying persons?
- How does forensic identification work?
- Exceptions to Mendel's Laws
- How Does Inheritance Work?
- Mutations and the Next Generation
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- The Influence of DNA Structure and Binding Domains
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- How Many Genes Do Humans Have?
- Structural Genes, Junk DNA, and Regulatory Sequences
- From Genes to Proteins: Start to Finish
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- The Core Gene Sequence: Introns and Exons
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- Why Study Mitochondria?
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- The Physical Structure of the Human Genome
- WHAT IS A GENOME?
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