Forensic DNA Mixtures, Approaches, and Analysis

2014 ◽  
pp. 216-231 ◽  
Keyword(s):  
2015 ◽  
Vol 16 ◽  
pp. 208-215 ◽  
Author(s):  
Lev Voskoboinik ◽  
Sheri B. Ayers ◽  
Aaron K. LeFebvre ◽  
Ariel Darvasi

2010 ◽  
Vol 56 (1) ◽  
pp. 23-28 ◽  
Author(s):  
Hinda Haned ◽  
Laurent Pène ◽  
Jean R. Lobry ◽  
Anne B. Dufour ◽  
Dominique Pontier

Author(s):  
R. G. Cowell ◽  
T. Graversen ◽  
S. L. Lauritzen ◽  
J. Mortera
Keyword(s):  

Author(s):  
Ullrich J. Monich ◽  
Catherine Grgicak ◽  
Viveck Cadambe ◽  
Jason Yonglin Wu ◽  
Genevieve Wellner ◽  
...  

2017 ◽  
Author(s):  
Darrell O. Ricke ◽  
Joe Isaacson ◽  
James Watkins ◽  
Philip Fremont-Smith ◽  
Tara Boettcher ◽  
...  

AbstractIdentification of individuals in complex DNA mixtures remains a challenge for forensic analysts. Recent advances in high throughput sequencing (HTS) are enabling analysis of DNA mixtures with expanded panels of Short Tandem Repeats (STRs) and/or Single Nucleotide Polymorphisms (SNPs). We present the plateau method for direct SNP DNA mixture deconvolution into sub-profiles based on differences in contributors’ DNA concentrations in the mixtures in the absence of matching reference profiles. The Plateau method can detect profiles of individuals whose contribution is as low as 1/200 in a DNA mixture (patent pending)1.


2020 ◽  
Vol 49 ◽  
pp. 102367 ◽  
Author(s):  
Fabio Oldoni ◽  
Drew Bader ◽  
Chiara Fantinato ◽  
Sharon C. Wootton ◽  
Robert Lagacé ◽  
...  
Keyword(s):  

2020 ◽  
Vol 7 (1) ◽  
pp. 111-142
Author(s):  
Julia Mortera

Forensic science has experienced a period of rapid change because of the tremendous evolution in DNA profiling. Problems of forensic identification from DNA evidence can become extremely challenging, both logically and computationally, in the presence of complicating features, such as in mixed DNA trace evidence. Additional complicating aspects are possible, such as missing data on individuals, heterogeneous populations, and kinship. In such cases, there is considerable uncertainty involved in determining whether or not the DNA of a given individual is actually present in the sample. We begin by giving a brief introduction to the genetic background needed for understanding forensic DNA mixtures, including the artifacts that commonly occur in the DNA amplification process. We then review different methods and software based on qualitative and quantitative information and give details on a quantitative method that uses Bayesian networks as a computational device for efficiently computing likelihoods. This method allows for the possibility of combining evidence from multiple samples to make inference about relationships from DNA mixtures and other more complex scenarios.


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