2022
DOI: 10.3390/genes13081429
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Internal Validation of MaSTR™ Probabilistic Genotyping Software for the Interpretation of 2–5 Person Mixed DNA Profiles

Abstract: Mixed human deoxyribonucleic acid (DNA) samples present one of the most challenging pieces of evidence that a forensic analyst can encounter. When multiple contributors, stochastic amplification, and allele drop-out further complicate the mixture profile, interpretation by hand becomes unreliable and statistical analysis problematic. Probabilistic genotyping software has provided a tool to address complex mixture interpretation and provide likelihood ratios for defined sets of propositions. The MaSTR™ software… Show more

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Cited by 8 publications
(3 citation statements)
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“…In the past three years, validation studies have been performed with a number of probabilistic genotyping software (PGS) systems including EuroForMix [ 278 ], DNAStatistX [ 279 , 280 ], TrueAllele [ 281 ], STRmix [ 282 ], Statistefix [ 283 ], Mixture Solution [ 284 ], Kongoh [ 285 ], and MaSTR [ 286 , 287 ]. Developers of EuroForMix, DNAStatistX, and STRmix provided a review of these systems [ 288 ].…”
Section: Advancements In Current Practicesmentioning
confidence: 99%
“…In the past three years, validation studies have been performed with a number of probabilistic genotyping software (PGS) systems including EuroForMix [ 278 ], DNAStatistX [ 279 , 280 ], TrueAllele [ 281 ], STRmix [ 282 ], Statistefix [ 283 ], Mixture Solution [ 284 ], Kongoh [ 285 ], and MaSTR [ 286 , 287 ]. Developers of EuroForMix, DNAStatistX, and STRmix provided a review of these systems [ 288 ].…”
Section: Advancements In Current Practicesmentioning
confidence: 99%
“…In the statistical analysis of peak height and peak area of the short tandem repeat (STR) typing analysis, factors such as DNA concentration and the proportion of mixed samples can impact the results, making it difficult to eliminate the influence of shadow bands, nonspecific bands, amplification imbalance, and allele imbalance [4,5]. Through the statistical analysis of mixed DNA profiles, it becomes possible to interpret the potential STR genotypes of each individual [5,6]. Additionally, Y-STR profiles can be assessed using a likelihood ratio method [7], although personal identification is not always possible.…”
Section: Introductionmentioning
confidence: 99%
“…Estimates of the number of contributors are less reliable for groups with lower genetic diversity 33 . Variation in LRs has been observed across broadly defined groups (all with relatively high genetic diversity) 32,34,35 . These results all suggest variability in the accuracy of mixture analysis across genetic backgrounds.…”
Section: Introductionmentioning
confidence: 99%