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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Veröffentlicht in:Scientific reports 2020-02, Vol.10 (1), p.1945-1945, Article 1945
Hauptverfasser: 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
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Sprache:eng
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Zusammenfassung: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.
ISSN:2045-2322
2045-2322
DOI:10.1038/s41598-020-58980-x