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P1: GPB Final Pages
 Encyclopedia of Physical Science and Technology  EN004L-956  June 9, 2001  21:7






               598                                                                           DNA Testing in Forensic Science







































                      FIGURE 6 The PCR process. Courtesy of PE Cetus Instruments. (From Schanfield, M. S. (2000). Deoxyribonucleic
                      Acid/Polymerase Chain Reaction. In “Encyclopedia of Forensic Sciences” (Siegel, J. A., Saukko, P. J., and Knupfer,
                      G. C., eds.), Academic Press, London, p. 517.)


               to be detected. This is a suggested method to verify if the  D8S1179, D13S317, D16S539, D18S51, D21S11, FGA,
               PCR amplification was successful and that there is a PCR  THO1, TPOX, and VWA03. These loci overlapped with
               product to detect.                                the Forensic Science Services multiplexes and the Interpol
                                                                 multiplexes. The 13 loci can be obtained in two amplifica-
                                                                 tions using Profiler Plus and Cofiler or in a single ampli-
               V. STRs USED FORENSICALLY
                                                                 fication using a kit in development called Identifiler from
               At this point in time with the large number of STR loci, a
                                                                 1 and Powerplex 2 from Promega (Table II), or in a single
               demand for a standardized panel in the United States, and
                                                                 reaction with Powerplex 16 by Promega.
               a need for there to be at least some sharing of loci with
               forensic counterparts in Canada, England, and Europe,
                                                                 A. Fluorescent Dyes
               the Technical Working Group on DNA Analysis Methods
               (TWGDAM) implemented a multi-laboratory evaluation  Before discussing the equipment used to detect fluorescent
               of those STR loci available in kits in the United States. The  STRs some understanding of fluorescent dyes are neces-
               loci chosen would be the PCR-based core of a national sex  sary. Fluorescent dyes or minerals when subjected to light
               offender file required under the 1994 DNA Identification  at one wave length, such as untraviolet light or black light,
               Act. The national program is called Combined DNA In-  will give off colored light at a slightly different wavelength
               dexing System or CODIS for short.                 or color. A characteristic of fluorescent dyes or materials
                 The TWGDAM/CODIS loci were announced at the     is that the compound is excited at one frequency of light,
               Promega DNA Identification Symposium in the fall of  referred to as its absorption or excitation peak, and emits
               1997 and at the American Academy of Forensic Sci-  or gives off light a different frequency, referred to as its
               ence meeting in February 1998. The following loci were  emission peak.
               chosen to be part of what was originally called the  To label a PCR primer with a fluorescent dye, the dye

               CODIS 13 loci: CSF1PO, D3S1358, D5S818, D7S820,   is attached to the 5 end of the molecule. Since DNA is
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