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Development and validation of open-source software for DNA mixture interpretation based on a quantitative continuous model

In criminal investigations, forensic scientists need to evaluate DNA mixtures. The estimation of the number of contributors and evaluation of the contribution of a person of interest (POI) from these samples are challenging. In this study, we developed a new open-source software “Kongoh” for interpr...

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Autores principales: Manabe, Sho, Morimoto, Chie, Hamano, Yuya, Fujimoto, Shuntaro, Tamaki, Keiji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5693437/
https://www.ncbi.nlm.nih.gov/pubmed/29149210
http://dx.doi.org/10.1371/journal.pone.0188183
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author Manabe, Sho
Morimoto, Chie
Hamano, Yuya
Fujimoto, Shuntaro
Tamaki, Keiji
author_facet Manabe, Sho
Morimoto, Chie
Hamano, Yuya
Fujimoto, Shuntaro
Tamaki, Keiji
author_sort Manabe, Sho
collection PubMed
description In criminal investigations, forensic scientists need to evaluate DNA mixtures. The estimation of the number of contributors and evaluation of the contribution of a person of interest (POI) from these samples are challenging. In this study, we developed a new open-source software “Kongoh” for interpreting DNA mixture based on a quantitative continuous model. The model uses quantitative information of peak heights in the DNA profile and considers the effect of artifacts and allelic drop-out. By using this software, the likelihoods of 1–4 persons’ contributions are calculated, and the most optimal number of contributors is automatically determined; this differs from other open-source software. Therefore, we can eliminate the need to manually determine the number of contributors before the analysis. Kongoh also considers allele- or locus-specific effects of biological parameters based on the experimental data. We then validated Kongoh by calculating the likelihood ratio (LR) of a POI’s contribution in true contributors and non-contributors by using 2–4 person mixtures analyzed through a 15 short tandem repeat typing system. Most LR values obtained from Kongoh during true-contributor testing strongly supported the POI’s contribution even for small amounts or degraded DNA samples. Kongoh correctly rejected a false hypothesis in the non-contributor testing, generated reproducible LR values, and demonstrated higher accuracy of the estimated number of contributors than another software based on the quantitative continuous model. Therefore, Kongoh is useful in accurately interpreting DNA evidence like mixtures and small amounts or degraded DNA samples.
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spelling pubmed-56934372017-11-30 Development and validation of open-source software for DNA mixture interpretation based on a quantitative continuous model Manabe, Sho Morimoto, Chie Hamano, Yuya Fujimoto, Shuntaro Tamaki, Keiji PLoS One Research Article In criminal investigations, forensic scientists need to evaluate DNA mixtures. The estimation of the number of contributors and evaluation of the contribution of a person of interest (POI) from these samples are challenging. In this study, we developed a new open-source software “Kongoh” for interpreting DNA mixture based on a quantitative continuous model. The model uses quantitative information of peak heights in the DNA profile and considers the effect of artifacts and allelic drop-out. By using this software, the likelihoods of 1–4 persons’ contributions are calculated, and the most optimal number of contributors is automatically determined; this differs from other open-source software. Therefore, we can eliminate the need to manually determine the number of contributors before the analysis. Kongoh also considers allele- or locus-specific effects of biological parameters based on the experimental data. We then validated Kongoh by calculating the likelihood ratio (LR) of a POI’s contribution in true contributors and non-contributors by using 2–4 person mixtures analyzed through a 15 short tandem repeat typing system. Most LR values obtained from Kongoh during true-contributor testing strongly supported the POI’s contribution even for small amounts or degraded DNA samples. Kongoh correctly rejected a false hypothesis in the non-contributor testing, generated reproducible LR values, and demonstrated higher accuracy of the estimated number of contributors than another software based on the quantitative continuous model. Therefore, Kongoh is useful in accurately interpreting DNA evidence like mixtures and small amounts or degraded DNA samples. Public Library of Science 2017-11-17 /pmc/articles/PMC5693437/ /pubmed/29149210 http://dx.doi.org/10.1371/journal.pone.0188183 Text en © 2017 Manabe et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Manabe, Sho
Morimoto, Chie
Hamano, Yuya
Fujimoto, Shuntaro
Tamaki, Keiji
Development and validation of open-source software for DNA mixture interpretation based on a quantitative continuous model
title Development and validation of open-source software for DNA mixture interpretation based on a quantitative continuous model
title_full Development and validation of open-source software for DNA mixture interpretation based on a quantitative continuous model
title_fullStr Development and validation of open-source software for DNA mixture interpretation based on a quantitative continuous model
title_full_unstemmed Development and validation of open-source software for DNA mixture interpretation based on a quantitative continuous model
title_short Development and validation of open-source software for DNA mixture interpretation based on a quantitative continuous model
title_sort development and validation of open-source software for dna mixture interpretation based on a quantitative continuous model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5693437/
https://www.ncbi.nlm.nih.gov/pubmed/29149210
http://dx.doi.org/10.1371/journal.pone.0188183
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