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A 124-plex Microhaplotype Panel Based on Next-generation Sequencing Developed for Forensic Applications

Microhaplotypes are an emerging type of forensic genetic marker that are expected to support multiple forensic applications. Here, we developed a 124-plex panel for microhaplotype genotyping based on next-generation sequencing (NGS). The panel yielded intralocus and interlocus balanced sequencing da...

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Autores principales: Pang, Jing-Bo, Rao, Min, Chen, Qing-Feng, Ji, An-Quan, Zhang, Chi, Kang, Ke-Lai, Wu, Hao, Ye, Jian, Nie, Sheng-Jie, Wang, Le
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7004988/
https://www.ncbi.nlm.nih.gov/pubmed/32029845
http://dx.doi.org/10.1038/s41598-020-58980-x
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author Pang, Jing-Bo
Rao, Min
Chen, Qing-Feng
Ji, An-Quan
Zhang, Chi
Kang, Ke-Lai
Wu, Hao
Ye, Jian
Nie, Sheng-Jie
Wang, Le
author_facet Pang, Jing-Bo
Rao, Min
Chen, Qing-Feng
Ji, An-Quan
Zhang, Chi
Kang, Ke-Lai
Wu, Hao
Ye, Jian
Nie, Sheng-Jie
Wang, Le
author_sort Pang, Jing-Bo
collection PubMed
description Microhaplotypes are an emerging type of forensic genetic marker that are expected to support multiple forensic applications. Here, we developed a 124-plex panel for microhaplotype genotyping based on next-generation sequencing (NGS). The panel yielded intralocus and interlocus balanced sequencing data with a high percentage of effective reads. A full genotype was determined with as little as 0.1 ng of input DNA. Parallel mixture experiments and in-depth comparative analyses were performed with capillary-electrophoresis-based short tandem repeat (STR) and NGS-based microhaplotype genotyping, and demonstrated that microhaplotypes are far superior to STRs for mixture deconvolution. DNA from Han Chinese individuals (n = 256) was sequenced with the 124-plex panel. In total, 514 alleles were observed, and the forensic genetic parameters were calculated. A comparison of the forensic parameters for the 20 microhaplotypes with the top A(e) values in the 124-plex panel and 20 commonly used forensic STRs showed that these microhaplotypes were as effective as STRs in identifying individuals. A linkage disequilibrium analysis showed that 106 of the 124 microhaplotypes were independently hereditary, and the combined match probability for these 106 microhaplotypes was 5.23 × 10(−66). We conclude that this 124-plex microhaplotype panel is a powerful tool for forensic applications.
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spelling pubmed-70049882020-02-14 A 124-plex Microhaplotype Panel Based on Next-generation Sequencing Developed for Forensic Applications Pang, Jing-Bo Rao, Min Chen, Qing-Feng Ji, An-Quan Zhang, Chi Kang, Ke-Lai Wu, Hao Ye, Jian Nie, Sheng-Jie Wang, Le Sci Rep Article Microhaplotypes are an emerging type of forensic genetic marker that are expected to support multiple forensic applications. Here, we developed a 124-plex panel for microhaplotype genotyping based on next-generation sequencing (NGS). The panel yielded intralocus and interlocus balanced sequencing data with a high percentage of effective reads. A full genotype was determined with as little as 0.1 ng of input DNA. Parallel mixture experiments and in-depth comparative analyses were performed with capillary-electrophoresis-based short tandem repeat (STR) and NGS-based microhaplotype genotyping, and demonstrated that microhaplotypes are far superior to STRs for mixture deconvolution. DNA from Han Chinese individuals (n = 256) was sequenced with the 124-plex panel. In total, 514 alleles were observed, and the forensic genetic parameters were calculated. A comparison of the forensic parameters for the 20 microhaplotypes with the top A(e) values in the 124-plex panel and 20 commonly used forensic STRs showed that these microhaplotypes were as effective as STRs in identifying individuals. A linkage disequilibrium analysis showed that 106 of the 124 microhaplotypes were independently hereditary, and the combined match probability for these 106 microhaplotypes was 5.23 × 10(−66). We conclude that this 124-plex microhaplotype panel is a powerful tool for forensic applications. Nature Publishing Group UK 2020-02-06 /pmc/articles/PMC7004988/ /pubmed/32029845 http://dx.doi.org/10.1038/s41598-020-58980-x Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Pang, Jing-Bo
Rao, Min
Chen, Qing-Feng
Ji, An-Quan
Zhang, Chi
Kang, Ke-Lai
Wu, Hao
Ye, Jian
Nie, Sheng-Jie
Wang, Le
A 124-plex Microhaplotype Panel Based on Next-generation Sequencing Developed for Forensic Applications
title A 124-plex Microhaplotype Panel Based on Next-generation Sequencing Developed for Forensic Applications
title_full A 124-plex Microhaplotype Panel Based on Next-generation Sequencing Developed for Forensic Applications
title_fullStr A 124-plex Microhaplotype Panel Based on Next-generation Sequencing Developed for Forensic Applications
title_full_unstemmed A 124-plex Microhaplotype Panel Based on Next-generation Sequencing Developed for Forensic Applications
title_short A 124-plex Microhaplotype Panel Based on Next-generation Sequencing Developed for Forensic Applications
title_sort 124-plex microhaplotype panel based on next-generation sequencing developed for forensic applications
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7004988/
https://www.ncbi.nlm.nih.gov/pubmed/32029845
http://dx.doi.org/10.1038/s41598-020-58980-x
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