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Electrophoresis. 2017 Mar;38(6):855-868. doi: 10.1002/elps.201600385. Epub 2017 Jan 17.

Exploring STR signal in the single- and multicopy number regimes: Deductions from an in silico model of the entire DNA laboratory process.

Author information

1
Hamilton Institute, Maynooth University, Maynooth, Ireland.
2
Research Laboratory of Electronics, Massachusetts Institute of Technology, Cambridge, MA, USA.
3
Biomedical Forensic Sciences, Boston University School of Medicine, Boston, MA, USA.

Abstract

Short tandem repeat (STR) profiling from DNA samples has long been the bedrock of human identification. The laboratory process is composed of multiple procedures that include quantification, sample dilution, PCR, electrophoresis, and fragment analysis. The end product is a short tandem repeat electropherogram comprised of signal from allele, artifacts, and instrument noise. In order to optimize or alter laboratory protocols, a large number of validation samples must be created at significant expense. As a tool to support that process and to enable the exploration of complex scenarios without costly sample creation, a mechanistic stochastic model that incorporates each of the aforementioned processing features is described herein. The model allows rapid in silico simulation of electropherograms from multicontributor samples and enables detailed investigations of involved scenarios. An implementation of the model that is parameterized by extensive laboratory data is publically available. To illustrate its utility, the model was employed in order to evaluate the effects of sample dilutions, injection time, and cycle number on peak height, and the nature of stutter ratios at low template. We verify the model's findings by comparison with experimentally generated data.

KEYWORDS:

Analytical threshold; Electropherogram signal model; Forensic DNA; Short tandem repeats; Single-copy DNA analysis

PMID:
27981603
DOI:
10.1002/elps.201600385
[Indexed for MEDLINE]

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