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Analysis of the genealogy process in forensic genetic genealogy
The genealogy process is typically the most time‐consuming part of—and a limiting factor in the success of—forensic genetic genealogy, which is a new approach to solving violent crimes and identifying human remains. We formulate a stochastic dynamic program that—given the list of matches and their g...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9826014/ https://www.ncbi.nlm.nih.gov/pubmed/36059116 http://dx.doi.org/10.1111/1556-4029.15127 |
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author | Ertürk, Mine Su Fitzpatrick, Colleen Press, Margaret Wein, Lawrence M. |
author_facet | Ertürk, Mine Su Fitzpatrick, Colleen Press, Margaret Wein, Lawrence M. |
author_sort | Ertürk, Mine Su |
collection | PubMed |
description | The genealogy process is typically the most time‐consuming part of—and a limiting factor in the success of—forensic genetic genealogy, which is a new approach to solving violent crimes and identifying human remains. We formulate a stochastic dynamic program that—given the list of matches and their genetic distances to the unknown target—chooses the best decision at each point in time: which match to investigate (i.e., find its ancestors and look for most recent common ancestors between the match and the target), which set of potential most recent common ancestors to descend from (i.e., find its descendants, with the goal of identifying a marriage between the maternal and paternal sides of the target's family tree), or whether to terminate the investigation. The objective is to maximize the probability of finding the target minus a cost associated with the expected size of the final family tree. We estimate the parameters of our model using data from 17 cases (eight solved, nine unsolved) from the DNA Doe Project. We assess the Proposed Strategy using simulated versions of the 17 DNA Doe Project cases, and compare it to a Benchmark Strategy that ranks matches by their genetic distance to the target and only descends from known common ancestors between a pair of matches. The Proposed Strategy solves cases ≈10 − fold faster than the Benchmark Strategy, and does so by aggressively descending from a set of potential most recent common ancestors between the target and a match even when this set has a low probability of containing the correct most recent common ancestor. Our analysis provides a mathematical foundation for improving the genealogy process in forensic genetic genealogy. |
format | Online Article Text |
id | pubmed-9826014 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98260142023-01-09 Analysis of the genealogy process in forensic genetic genealogy Ertürk, Mine Su Fitzpatrick, Colleen Press, Margaret Wein, Lawrence M. J Forensic Sci Original Papers The genealogy process is typically the most time‐consuming part of—and a limiting factor in the success of—forensic genetic genealogy, which is a new approach to solving violent crimes and identifying human remains. We formulate a stochastic dynamic program that—given the list of matches and their genetic distances to the unknown target—chooses the best decision at each point in time: which match to investigate (i.e., find its ancestors and look for most recent common ancestors between the match and the target), which set of potential most recent common ancestors to descend from (i.e., find its descendants, with the goal of identifying a marriage between the maternal and paternal sides of the target's family tree), or whether to terminate the investigation. The objective is to maximize the probability of finding the target minus a cost associated with the expected size of the final family tree. We estimate the parameters of our model using data from 17 cases (eight solved, nine unsolved) from the DNA Doe Project. We assess the Proposed Strategy using simulated versions of the 17 DNA Doe Project cases, and compare it to a Benchmark Strategy that ranks matches by their genetic distance to the target and only descends from known common ancestors between a pair of matches. The Proposed Strategy solves cases ≈10 − fold faster than the Benchmark Strategy, and does so by aggressively descending from a set of potential most recent common ancestors between the target and a match even when this set has a low probability of containing the correct most recent common ancestor. Our analysis provides a mathematical foundation for improving the genealogy process in forensic genetic genealogy. John Wiley and Sons Inc. 2022-09-04 2022-11 /pmc/articles/PMC9826014/ /pubmed/36059116 http://dx.doi.org/10.1111/1556-4029.15127 Text en © 2022 The Authors. Journal of Forensic Sciences published by Wiley Periodicals LLC on behalf of American Academy of Forensic Sciences. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Papers Ertürk, Mine Su Fitzpatrick, Colleen Press, Margaret Wein, Lawrence M. Analysis of the genealogy process in forensic genetic genealogy |
title | Analysis of the genealogy process in forensic genetic genealogy |
title_full | Analysis of the genealogy process in forensic genetic genealogy |
title_fullStr | Analysis of the genealogy process in forensic genetic genealogy |
title_full_unstemmed | Analysis of the genealogy process in forensic genetic genealogy |
title_short | Analysis of the genealogy process in forensic genetic genealogy |
title_sort | analysis of the genealogy process in forensic genetic genealogy |
topic | Original Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9826014/ https://www.ncbi.nlm.nih.gov/pubmed/36059116 http://dx.doi.org/10.1111/1556-4029.15127 |
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