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Improving the Utilization of STRmix™ Variance Parameters as Semi-Quantitative Profile Modeling Metrics
Distributions of the variance parameter values developed during the validation process. Comparisons of these prior distributions to the run-specific average are one measure used by analysts to assess the reliability of a STRmix deconvolution. This study examined the behavior of three different STRmi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9859078/ https://www.ncbi.nlm.nih.gov/pubmed/36672842 http://dx.doi.org/10.3390/genes14010102 |
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author | Duke, Kyle Myers, Steven Cuenca, Daniela Wallin, Jeanette |
author_facet | Duke, Kyle Myers, Steven Cuenca, Daniela Wallin, Jeanette |
author_sort | Duke, Kyle |
collection | PubMed |
description | Distributions of the variance parameter values developed during the validation process. Comparisons of these prior distributions to the run-specific average are one measure used by analysts to assess the reliability of a STRmix deconvolution. This study examined the behavior of three different STRmix variance parameters under standard amplification and interpretation conditions, as well as under a variety of challenging conditions, with the goal of making comparisons to the prior distributions more practical and meaningful. Using information found in STRmix v2.8 Interpretation Reports, we plotted the log(10) of each variance parameter against the log(10) of the template amount of the highest-level contributor (Tc) for a large set of mixture data amplified under standard conditions. We observed nonlinear trends in these plots, which we regressed to fourth-order polynomials, and used the regression data to establish typical ranges for the variance parameters over the Tc range. We then compared the typical variance parameter ranges to log(10)(variance parameter) v log(10)(Tc) plots for mixtures amplified and interpreted under a variety of challenging conditions. We observed several distinct patterns to variance parameter shifts in the challenged data interpretations in comparison to the unchallenged data interpretations, as well as distinct shifts in the unchallenged variance parameters away from their prior gamma distribution modes over specific ranges of Tc. These findings suggest that employing empirically determined working ranges for variance parameters may be an improved means of detecting whether aberrations in the interpretation were meaningful enough to trigger greater scrutiny of the electropherogram and genotype interpretation. |
format | Online Article Text |
id | pubmed-9859078 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-98590782023-01-21 Improving the Utilization of STRmix™ Variance Parameters as Semi-Quantitative Profile Modeling Metrics Duke, Kyle Myers, Steven Cuenca, Daniela Wallin, Jeanette Genes (Basel) Article Distributions of the variance parameter values developed during the validation process. Comparisons of these prior distributions to the run-specific average are one measure used by analysts to assess the reliability of a STRmix deconvolution. This study examined the behavior of three different STRmix variance parameters under standard amplification and interpretation conditions, as well as under a variety of challenging conditions, with the goal of making comparisons to the prior distributions more practical and meaningful. Using information found in STRmix v2.8 Interpretation Reports, we plotted the log(10) of each variance parameter against the log(10) of the template amount of the highest-level contributor (Tc) for a large set of mixture data amplified under standard conditions. We observed nonlinear trends in these plots, which we regressed to fourth-order polynomials, and used the regression data to establish typical ranges for the variance parameters over the Tc range. We then compared the typical variance parameter ranges to log(10)(variance parameter) v log(10)(Tc) plots for mixtures amplified and interpreted under a variety of challenging conditions. We observed several distinct patterns to variance parameter shifts in the challenged data interpretations in comparison to the unchallenged data interpretations, as well as distinct shifts in the unchallenged variance parameters away from their prior gamma distribution modes over specific ranges of Tc. These findings suggest that employing empirically determined working ranges for variance parameters may be an improved means of detecting whether aberrations in the interpretation were meaningful enough to trigger greater scrutiny of the electropherogram and genotype interpretation. MDPI 2022-12-29 /pmc/articles/PMC9859078/ /pubmed/36672842 http://dx.doi.org/10.3390/genes14010102 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Duke, Kyle Myers, Steven Cuenca, Daniela Wallin, Jeanette Improving the Utilization of STRmix™ Variance Parameters as Semi-Quantitative Profile Modeling Metrics |
title | Improving the Utilization of STRmix™ Variance Parameters as Semi-Quantitative Profile Modeling Metrics |
title_full | Improving the Utilization of STRmix™ Variance Parameters as Semi-Quantitative Profile Modeling Metrics |
title_fullStr | Improving the Utilization of STRmix™ Variance Parameters as Semi-Quantitative Profile Modeling Metrics |
title_full_unstemmed | Improving the Utilization of STRmix™ Variance Parameters as Semi-Quantitative Profile Modeling Metrics |
title_short | Improving the Utilization of STRmix™ Variance Parameters as Semi-Quantitative Profile Modeling Metrics |
title_sort | improving the utilization of strmix™ variance parameters as semi-quantitative profile modeling metrics |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9859078/ https://www.ncbi.nlm.nih.gov/pubmed/36672842 http://dx.doi.org/10.3390/genes14010102 |
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