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Population Analysis with the GenePrinttm STR Multiplex Systems

 

Katherine A. Micka1, Steve Creacy2, Cynthia J. Sprecher1, Robert A. Bever2, and James W. Schumm1
1Promega Corporation, Madison, WI
2Genetic Design, Inc., Greensboro, NC

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We describe the powerful, sensitive, high throughput, nonisotopic methods for DNA analyses based upon the amplification of polymorphic short tandem repeat (STR) loci. We have developed three systems for silver stain detection without instrumentation, (CTT) CSF1PO, TPOX, TH01, (FFv) F13A01, FESFPS, vWA, and (SilverSTRtm III) D16S539, D7S820, D13S317. In addition, we have developed three fluorescein-labeled quadriplex systems: (CTTv) CSF1PO, TPOX, TH01, vWA, (FFFL) F13A01, FESFPS, F13B, LPL, and (GammaSTRtm) D16S539, D7S820, D13S317, D5S818. A two-color, eight locus system, the GenePrinttm PowerPlextm System, has also been developed. The fluorescent and silver stain systems have been designed to contain the same loci whenever possible (see chart below).

CSF1P0

TH01

TPOX

VA

F13A01

FESFPS

F13B

LPL

D5S818

D7S820

D13S317

D16S539

Silver Multiplexes

CTT

FFv

   

SilverSTRtm III

 
Fluorescent Mulitplexes

CTTv

FFFL

GammaSTRtm

PowerPlextm

Analysis of over 200 individuals in each of three racial/ethnic groups indicates that using either the three silver multiplexes or the PowerPlextm System alone, the Matching Probability exceeds 1 in 100,000,000 in each population. Likewise, the Typical Paternity Index for these same combinations exceeds 300 in each population. The combination of the PowerPlextm System and FFFL generate numbers greater than 1 in 100,000,000,000 and 5,000, for Matching Probability and Typical Paternity Index, respectively, regardless of the population tested.

In sum, while providing a rapid and accurate assay requiring very little DNA template, these combinations of multiplexes, or the individual PowerPlextm System, provide the statistical power required for forensic and paternity applications.

 


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