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Anthropological analyses of 30 insertion/deletion autosomal markers in five major ethnic groups of Pakistan
We investigated the forensic efficacy of the 30 insertion/deletion (Indel) markers included in the Qiagen Investigator® DIPplex kit in 529 Pakistani individuals from five major subpopulations in Pakistan (Punjabi, Pashtun, Sindhi, Saraiki, and Baloch). In the Sindhi population, the distribution of H...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Taylor & Francis
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9245971/ https://www.ncbi.nlm.nih.gov/pubmed/35784406 http://dx.doi.org/10.1080/20961790.2021.1933366 |
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author | Shan, Muhammad Adnan Mechlenborg, Julie Røgen, Rebecca Børsting, Claus Morling, Niels |
author_facet | Shan, Muhammad Adnan Mechlenborg, Julie Røgen, Rebecca Børsting, Claus Morling, Niels |
author_sort | Shan, Muhammad Adnan |
collection | PubMed |
description | We investigated the forensic efficacy of the 30 insertion/deletion (Indel) markers included in the Qiagen Investigator® DIPplex kit in 529 Pakistani individuals from five major subpopulations in Pakistan (Punjabi, Pashtun, Sindhi, Saraiki, and Baloch). In the Sindhi population, the distribution of HLD81 and HLD97 alleles deviated from Hardy-Weinberg equilibrium after Bonferroni correction. The combined match probability ranged from 2.0E-12 (Pashtun and Baloch) to 1.0E-12 (Sindhi), and the mean paternity exclusion power varied from 0.995 (Punjabi, Sindhi, and Saraiki) to 0.996 (Pashtun and Baloch). The high combined power of discrimination (0.999 999 999 999 97) and low combined match probability (1.7E-12) for all subpopulations studied support the utility of the 30 Indel markers for forensic identification in the studied subpopulations. The allele frequencies of the Indel markers in the Pakistani subpopulations were compared with those from 18 other populations. The results show that the populations clustered according to geography. The subpopulations investigated in this work showed a close genetic relationship with others from Pakistan, as well as with South Central Asian and Middle Eastern populations. The results suggest that the Investigator(®) DIPplex kit can be useful as a supplementary tool for human identification in the five Pakistani subpopulations investigated in this study. Supplemental data for this article is available online at https://doi.org/10.1080/20961790.2021.1933366 . |
format | Online Article Text |
id | pubmed-9245971 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-92459712022-07-01 Anthropological analyses of 30 insertion/deletion autosomal markers in five major ethnic groups of Pakistan Shan, Muhammad Adnan Mechlenborg, Julie Røgen, Rebecca Børsting, Claus Morling, Niels Forensic Sci Res Original Articles We investigated the forensic efficacy of the 30 insertion/deletion (Indel) markers included in the Qiagen Investigator® DIPplex kit in 529 Pakistani individuals from five major subpopulations in Pakistan (Punjabi, Pashtun, Sindhi, Saraiki, and Baloch). In the Sindhi population, the distribution of HLD81 and HLD97 alleles deviated from Hardy-Weinberg equilibrium after Bonferroni correction. The combined match probability ranged from 2.0E-12 (Pashtun and Baloch) to 1.0E-12 (Sindhi), and the mean paternity exclusion power varied from 0.995 (Punjabi, Sindhi, and Saraiki) to 0.996 (Pashtun and Baloch). The high combined power of discrimination (0.999 999 999 999 97) and low combined match probability (1.7E-12) for all subpopulations studied support the utility of the 30 Indel markers for forensic identification in the studied subpopulations. The allele frequencies of the Indel markers in the Pakistani subpopulations were compared with those from 18 other populations. The results show that the populations clustered according to geography. The subpopulations investigated in this work showed a close genetic relationship with others from Pakistan, as well as with South Central Asian and Middle Eastern populations. The results suggest that the Investigator(®) DIPplex kit can be useful as a supplementary tool for human identification in the five Pakistani subpopulations investigated in this study. Supplemental data for this article is available online at https://doi.org/10.1080/20961790.2021.1933366 . Taylor & Francis 2021-08-28 /pmc/articles/PMC9245971/ /pubmed/35784406 http://dx.doi.org/10.1080/20961790.2021.1933366 Text en © 2021 The Author(s). Published by Taylor & Francis Group on behalf of the Academy of Forensic Science. https://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/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Shan, Muhammad Adnan Mechlenborg, Julie Røgen, Rebecca Børsting, Claus Morling, Niels Anthropological analyses of 30 insertion/deletion autosomal markers in five major ethnic groups of Pakistan |
title | Anthropological analyses of 30 insertion/deletion autosomal markers in five major ethnic groups of Pakistan |
title_full | Anthropological analyses of 30 insertion/deletion autosomal markers in five major ethnic groups of Pakistan |
title_fullStr | Anthropological analyses of 30 insertion/deletion autosomal markers in five major ethnic groups of Pakistan |
title_full_unstemmed | Anthropological analyses of 30 insertion/deletion autosomal markers in five major ethnic groups of Pakistan |
title_short | Anthropological analyses of 30 insertion/deletion autosomal markers in five major ethnic groups of Pakistan |
title_sort | anthropological analyses of 30 insertion/deletion autosomal markers in five major ethnic groups of pakistan |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9245971/ https://www.ncbi.nlm.nih.gov/pubmed/35784406 http://dx.doi.org/10.1080/20961790.2021.1933366 |
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