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Developmental Validation of the Novel Five-Dye-Labeled Multiplex Autosomal STR Panel and Its Forensic Efficiency Evaluation

Short tandem repeats (STRs) are the most frequently used genetic markers in forensic genetics due to their high genetic diversities and abundant distributions in the human genome. Currently, the combined DNA index system is commonly incorporated into various commercial kits for forensic research. So...

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Autores principales: Huang, Shimei, Jin, Xiaoye, Zhang, Hongling, Jin, Haiying, Ren, Zheng, Wang, Qiyan, Liu, Yubo, Ji, Jingyan, Yang, Meiqing, Zhang, Han, Zheng, Xingkai, Song, Danlu, Zheng, Bingjie, Huang, Jiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9194853/
https://www.ncbi.nlm.nih.gov/pubmed/35711918
http://dx.doi.org/10.3389/fgene.2022.897650
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author Huang, Shimei
Jin, Xiaoye
Zhang, Hongling
Jin, Haiying
Ren, Zheng
Wang, Qiyan
Liu, Yubo
Ji, Jingyan
Yang, Meiqing
Zhang, Han
Zheng, Xingkai
Song, Danlu
Zheng, Bingjie
Huang, Jiang
author_facet Huang, Shimei
Jin, Xiaoye
Zhang, Hongling
Jin, Haiying
Ren, Zheng
Wang, Qiyan
Liu, Yubo
Ji, Jingyan
Yang, Meiqing
Zhang, Han
Zheng, Xingkai
Song, Danlu
Zheng, Bingjie
Huang, Jiang
author_sort Huang, Shimei
collection PubMed
description Short tandem repeats (STRs) are the most frequently used genetic markers in forensic genetics due to their high genetic diversities and abundant distributions in the human genome. Currently, the combined DNA index system is commonly incorporated into various commercial kits for forensic research. Some novel STRs that are different from the combined DNA index system were not only used to assess complex paternity cases but also could provide more genetic information and higher forensic efficiency in combination with those commonly used STRs. In this study, we validated forensic performance of a novel multiplex amplification STR panel to evaluate its sensitivity, species specificity, forensic application values, and so on. Obtained results revealed that the kit showed high sensitivity, and the complete allelic profile could be observed at 0.125 ng DNA sample. In addition, the kit possessed high species specificity, good tolerance to common inhibitors, and accurate genotyping ability. More importantly, STRs out of the kit displayed high discrimination power and probability of exclusion. To sum up, the novel kit presented in this study can be viewed as a promising tool for forensic human identification and complex paternity analysis.
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spelling pubmed-91948532022-06-15 Developmental Validation of the Novel Five-Dye-Labeled Multiplex Autosomal STR Panel and Its Forensic Efficiency Evaluation Huang, Shimei Jin, Xiaoye Zhang, Hongling Jin, Haiying Ren, Zheng Wang, Qiyan Liu, Yubo Ji, Jingyan Yang, Meiqing Zhang, Han Zheng, Xingkai Song, Danlu Zheng, Bingjie Huang, Jiang Front Genet Genetics Short tandem repeats (STRs) are the most frequently used genetic markers in forensic genetics due to their high genetic diversities and abundant distributions in the human genome. Currently, the combined DNA index system is commonly incorporated into various commercial kits for forensic research. Some novel STRs that are different from the combined DNA index system were not only used to assess complex paternity cases but also could provide more genetic information and higher forensic efficiency in combination with those commonly used STRs. In this study, we validated forensic performance of a novel multiplex amplification STR panel to evaluate its sensitivity, species specificity, forensic application values, and so on. Obtained results revealed that the kit showed high sensitivity, and the complete allelic profile could be observed at 0.125 ng DNA sample. In addition, the kit possessed high species specificity, good tolerance to common inhibitors, and accurate genotyping ability. More importantly, STRs out of the kit displayed high discrimination power and probability of exclusion. To sum up, the novel kit presented in this study can be viewed as a promising tool for forensic human identification and complex paternity analysis. Frontiers Media S.A. 2022-05-31 /pmc/articles/PMC9194853/ /pubmed/35711918 http://dx.doi.org/10.3389/fgene.2022.897650 Text en Copyright © 2022 Huang, Jin, Zhang, Jin, Ren, Wang, Liu, Ji, Yang, Zhang, Zheng, Song, Zheng and Huang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Huang, Shimei
Jin, Xiaoye
Zhang, Hongling
Jin, Haiying
Ren, Zheng
Wang, Qiyan
Liu, Yubo
Ji, Jingyan
Yang, Meiqing
Zhang, Han
Zheng, Xingkai
Song, Danlu
Zheng, Bingjie
Huang, Jiang
Developmental Validation of the Novel Five-Dye-Labeled Multiplex Autosomal STR Panel and Its Forensic Efficiency Evaluation
title Developmental Validation of the Novel Five-Dye-Labeled Multiplex Autosomal STR Panel and Its Forensic Efficiency Evaluation
title_full Developmental Validation of the Novel Five-Dye-Labeled Multiplex Autosomal STR Panel and Its Forensic Efficiency Evaluation
title_fullStr Developmental Validation of the Novel Five-Dye-Labeled Multiplex Autosomal STR Panel and Its Forensic Efficiency Evaluation
title_full_unstemmed Developmental Validation of the Novel Five-Dye-Labeled Multiplex Autosomal STR Panel and Its Forensic Efficiency Evaluation
title_short Developmental Validation of the Novel Five-Dye-Labeled Multiplex Autosomal STR Panel and Its Forensic Efficiency Evaluation
title_sort developmental validation of the novel five-dye-labeled multiplex autosomal str panel and its forensic efficiency evaluation
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9194853/
https://www.ncbi.nlm.nih.gov/pubmed/35711918
http://dx.doi.org/10.3389/fgene.2022.897650
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