Volume 27, Issue 2 p. 409-415
Research Article

Unknown biological mixtures evaluation using STR analytical quantification

Sadeep Shrestha

Sadeep Shrestha

Laboratory of Genomic Diversity, National Cancer Institute at Frederick, Frederick, MD, USA

Basic Research Program, SAIC-Frederick, National Cancer Institute at Frederick, Frederick, MD, USA

Department of Epidemiology, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD, USA

Current address: Department of Epidemiology, School of Public Health, University of Alabama at Birmingham, Birmingham, AL 35294, USA

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Steffanie A. Strathdee

Steffanie A. Strathdee

Department of Epidemiology, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD, USA

Division of International Health and Cross Cultural Medicine, University of California, San Diego, La Jolla, CA, USA

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Karl W. Broman

Karl W. Broman

Department of Biostatistics, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD, USA

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Michael W. Smith Dr.

Corresponding Author

Michael W. Smith Dr.

Laboratory of Genomic Diversity, National Cancer Institute at Frederick, Frederick, MD, USA

Basic Research Program, SAIC-Frederick, National Cancer Institute at Frederick, Frederick, MD, USA

SAIC-Frederick, National Cancer Institute at Frederick, Bldg 560, Rm 21–74, Frederick, MD 21702, USA Fax: +1-301-846-1909===Search for more papers by this author
First published: 25 January 2006
Citations: 4

Abstract

Allelic quantification of STRs, where the presence of three or more alleles represents mixtures, provides a novel method to identify mixtures from unknown biological sources. The allelic stutters resulting in slightly different repeat containing products during fragment amplification can be mistaken for true alleles complicating a simple approach to mixture analysis. An algorithm based on the array of estimated stutters from known samples was developed and tuned to maximize the identification of true nonmixtures through the analysis of three pentanucleotide STRs. Laboratory simulated scenarios of needle sharing generated 58 mixture and 38 nonmixture samples that were blinded for determining the number of alleles. Through developing and applying an algorithm that additively estimates stuttering around the two highest peaks, mixtures and nonmixtures were characterized with sensitivity of 77.5, 82.7 and 58% while maintaining the high specificity of 100, 97.4 and 100 for the W, X, and Z STRs individually. When all three STRs were used collectively, the resulting sensitivity and specificity was 91.4 and 97.4%, respectively. The newly validated approach of using multiple STRs as highly informative biomarkers in unknown sample mixture analyses has potential applications in genetics, forensic science, and epidemiological studies.