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Bright, J.-A.

Publications and source records attributed to Bright, J.-A..

2 recordsLinked to original sources

Testing methods for quantifying Monte Carlo variation for categorical variables in Probabilistic Genotyping

Two methods for applying a lower bound to the variation induced by the Monte Carlo effect are trialled. One of these is implemented in the widely used probabilistic genotyping system, STRmix. Neither approach is giving the desired 99% coverage. In some cases the coverage is much lower than the desired 99%. The discrepancy (i.e. the distance between the LR corresponding to the desired coverage and the LR observed coverage at 99%) is not large. For example, the discrepancy of 0.23 for approach 1 suggests the lower bounds should be moved downwards by a factor of 1.7 to achieve the desired 99% coverage. Although less effective than desired these methods provide a layer of conservatism that is additional to the other layers. These other layers are from factors such as the conservatism within the sub-population model, the choice of conservative measures of co-ancestry, the consideration of relatives within the population and the resampling method used for allele probabilities, all of which tend to understate the strength of the findings. HighlightsO_LITwo methods for quantifying Monte Carlo variability are tested, C_LIO_LIBoth give less than the desired 99% coverage, C_LIO_LIThe magnitude of possible discrepancy is small, C_LIO_LIFor example an LR of 4.3 x 1011 could be reported as 1.8 x 1012 C_LIO_LIAn LR of 18 could be reported as 22. C_LI

molecular biology↗

Revisiting the STRmixlikelihood ratio probability interval coverage considering multiple factors

In previously reported work a method for applying a lower bound to the variation induced by the Monte Carlo effect was trialled. This is implemented in the widely used probabilistic genotyping system, STRmix. The approach did not give the desired 99% coverage. However, the method for assigning the lower bound to the MCMC variability is only one of a number of layers of conservativism applied in a typical application. We tested all but one of these sources of variability collectively and term the result the near global coverage. The near global coverage for all tested samples was greater than 99.5% for inclusionary average LRs of known donors. This suggests that when included in the probability interval method the other layers of conservativism are more than adequate to compensate for the intermittent underperformance of the MCMC variability component. Running for extended MCMC accepts was also shown to result in improved precision.

molecular biology↗