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Multi-Indel: A Microhaplotype Marker Can Be Typed Using Capillary Electrophoresis Platforms

Since the concept of microhaplotypes was proposed by Kidd in 2013, various microhaplotype markers have been investigated for various forensic purposes, such as individual identification, deconvolution of DNA mixtures, or forensic ancestry inference. In our opinion, various compound markers are also...

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Autores principales: Qu, Shengqiu, Lv, Meili, Xue, Jiaming, Zhu, Jing, Wang, Li, Jian, Hui, Liu, Yuqing, Zhang, Ranran, Zha, Lagabaiyila, Liang, Weibo, Zhang, Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7649793/
https://www.ncbi.nlm.nih.gov/pubmed/33193656
http://dx.doi.org/10.3389/fgene.2020.567082
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author Qu, Shengqiu
Lv, Meili
Xue, Jiaming
Zhu, Jing
Wang, Li
Jian, Hui
Liu, Yuqing
Zhang, Ranran
Zha, Lagabaiyila
Liang, Weibo
Zhang, Lin
author_facet Qu, Shengqiu
Lv, Meili
Xue, Jiaming
Zhu, Jing
Wang, Li
Jian, Hui
Liu, Yuqing
Zhang, Ranran
Zha, Lagabaiyila
Liang, Weibo
Zhang, Lin
author_sort Qu, Shengqiu
collection PubMed
description Since the concept of microhaplotypes was proposed by Kidd in 2013, various microhaplotype markers have been investigated for various forensic purposes, such as individual identification, deconvolution of DNA mixtures, or forensic ancestry inference. In our opinion, various compound markers are also regarded as generalized microhaplotypes, encompassing two or more variants in a short segment of DNA (e.g., 200 bp). That is, a set of variants (referred to herein as multi-variants) within a certain length includes single nucleotide polymorphisms (SNP), insertion/deletion polymorphisms (Indels), or short tandem repeat polymorphisms (STRs). At present, multi-variant is mainly aimed at multi-SNPs. However, the haplotype genotyping of multi-variants relies on single-strand analysis, mainly using massively parallel sequencing (MPS). Here, we describe a method based on a capillary electrophoresis (CE) platform that can directly obtain haplotypes of individuals. Several microhaplotypes consisting of three or more Indels with different insertion or deletion lengths in the range of less than 200 bp were screened out, each of which had at least three haplotypes. As a result, the haplotype of an individual was reflected by the length of its polymorphism. Finally, we established a multiplex amplification system containing 18 multi-Indel markers that could identify haplotypes on each chromosome of an individual. The combined power of discrimination (CPD) and the cumulative probability of exclusion (CPE) were 0.999999999997234 and 0.9984, respectively.
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spelling pubmed-76497932020-11-13 Multi-Indel: A Microhaplotype Marker Can Be Typed Using Capillary Electrophoresis Platforms Qu, Shengqiu Lv, Meili Xue, Jiaming Zhu, Jing Wang, Li Jian, Hui Liu, Yuqing Zhang, Ranran Zha, Lagabaiyila Liang, Weibo Zhang, Lin Front Genet Genetics Since the concept of microhaplotypes was proposed by Kidd in 2013, various microhaplotype markers have been investigated for various forensic purposes, such as individual identification, deconvolution of DNA mixtures, or forensic ancestry inference. In our opinion, various compound markers are also regarded as generalized microhaplotypes, encompassing two or more variants in a short segment of DNA (e.g., 200 bp). That is, a set of variants (referred to herein as multi-variants) within a certain length includes single nucleotide polymorphisms (SNP), insertion/deletion polymorphisms (Indels), or short tandem repeat polymorphisms (STRs). At present, multi-variant is mainly aimed at multi-SNPs. However, the haplotype genotyping of multi-variants relies on single-strand analysis, mainly using massively parallel sequencing (MPS). Here, we describe a method based on a capillary electrophoresis (CE) platform that can directly obtain haplotypes of individuals. Several microhaplotypes consisting of three or more Indels with different insertion or deletion lengths in the range of less than 200 bp were screened out, each of which had at least three haplotypes. As a result, the haplotype of an individual was reflected by the length of its polymorphism. Finally, we established a multiplex amplification system containing 18 multi-Indel markers that could identify haplotypes on each chromosome of an individual. The combined power of discrimination (CPD) and the cumulative probability of exclusion (CPE) were 0.999999999997234 and 0.9984, respectively. Frontiers Media S.A. 2020-10-23 /pmc/articles/PMC7649793/ /pubmed/33193656 http://dx.doi.org/10.3389/fgene.2020.567082 Text en Copyright © 2020 Qu, Lv, Xue, Zhu, Wang, Jian, Liu, Zhang, Zha, Liang and Zhang. http://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
Qu, Shengqiu
Lv, Meili
Xue, Jiaming
Zhu, Jing
Wang, Li
Jian, Hui
Liu, Yuqing
Zhang, Ranran
Zha, Lagabaiyila
Liang, Weibo
Zhang, Lin
Multi-Indel: A Microhaplotype Marker Can Be Typed Using Capillary Electrophoresis Platforms
title Multi-Indel: A Microhaplotype Marker Can Be Typed Using Capillary Electrophoresis Platforms
title_full Multi-Indel: A Microhaplotype Marker Can Be Typed Using Capillary Electrophoresis Platforms
title_fullStr Multi-Indel: A Microhaplotype Marker Can Be Typed Using Capillary Electrophoresis Platforms
title_full_unstemmed Multi-Indel: A Microhaplotype Marker Can Be Typed Using Capillary Electrophoresis Platforms
title_short Multi-Indel: A Microhaplotype Marker Can Be Typed Using Capillary Electrophoresis Platforms
title_sort multi-indel: a microhaplotype marker can be typed using capillary electrophoresis platforms
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7649793/
https://www.ncbi.nlm.nih.gov/pubmed/33193656
http://dx.doi.org/10.3389/fgene.2020.567082
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