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The population genetics characteristics of a 90 locus panel of microhaplotypes
Single-nucleotide polymorphisms (SNPs) and small genomic regions with multiple SNPs (microhaplotypes, MHs) are rapidly emerging as novel forensic investigative tools to assist in individual identification, kinship analyses, ancestry inference, and deconvolution of DNA mixtures. Here, we analyzed inf...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Berlin Heidelberg
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8553733/ https://www.ncbi.nlm.nih.gov/pubmed/34643790 http://dx.doi.org/10.1007/s00439-021-02382-0 |
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author | Pakstis, Andrew J. Gandotra, Neeru Speed, William C. Murtha, Michael Scharfe, Curt Kidd, Kenneth K. |
author_facet | Pakstis, Andrew J. Gandotra, Neeru Speed, William C. Murtha, Michael Scharfe, Curt Kidd, Kenneth K. |
author_sort | Pakstis, Andrew J. |
collection | PubMed |
description | Single-nucleotide polymorphisms (SNPs) and small genomic regions with multiple SNPs (microhaplotypes, MHs) are rapidly emerging as novel forensic investigative tools to assist in individual identification, kinship analyses, ancestry inference, and deconvolution of DNA mixtures. Here, we analyzed information for 90 microhaplotype loci in 4009 individuals from 79 world populations in 6 major biogeographic regions. The study included multiplex microhaplotype sequencing (mMHseq) data analyzed for 524 individuals from 16 populations and genotype data for 3485 individuals from 63 populations curated from public repositories. Analyses of the 79 populations revealed excellent characteristics for this 90-plex MH panel for various forensic applications achieving an overall average effective number of allele values (A(e)) of 4.55 (range 1.04–19.27) for individualization and mixture deconvolution. Population-specific random match probabilities ranged from a low of 10(–115) to a maximum of 10(–66). Mean informativeness (I(n)) for ancestry inference was 0.355 (range 0.117–0.883). 65 novel SNPs were detected in 39 of the MHs using mMHseq. Of the 3018 different microhaplotype alleles identified, 1337 occurred at frequencies > 5% in at least one of the populations studied. The 90-plex MH panel enables effective differentiation of population groupings for major biogeographic regions as well as delineation of distinct subgroupings within regions. Open-source, web-based software is available to support validation of this technology for forensic case work analysis and to tailor MH analysis for specific geographical regions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00439-021-02382-0. |
format | Online Article Text |
id | pubmed-8553733 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-85537332021-11-04 The population genetics characteristics of a 90 locus panel of microhaplotypes Pakstis, Andrew J. Gandotra, Neeru Speed, William C. Murtha, Michael Scharfe, Curt Kidd, Kenneth K. Hum Genet Original Investigation Single-nucleotide polymorphisms (SNPs) and small genomic regions with multiple SNPs (microhaplotypes, MHs) are rapidly emerging as novel forensic investigative tools to assist in individual identification, kinship analyses, ancestry inference, and deconvolution of DNA mixtures. Here, we analyzed information for 90 microhaplotype loci in 4009 individuals from 79 world populations in 6 major biogeographic regions. The study included multiplex microhaplotype sequencing (mMHseq) data analyzed for 524 individuals from 16 populations and genotype data for 3485 individuals from 63 populations curated from public repositories. Analyses of the 79 populations revealed excellent characteristics for this 90-plex MH panel for various forensic applications achieving an overall average effective number of allele values (A(e)) of 4.55 (range 1.04–19.27) for individualization and mixture deconvolution. Population-specific random match probabilities ranged from a low of 10(–115) to a maximum of 10(–66). Mean informativeness (I(n)) for ancestry inference was 0.355 (range 0.117–0.883). 65 novel SNPs were detected in 39 of the MHs using mMHseq. Of the 3018 different microhaplotype alleles identified, 1337 occurred at frequencies > 5% in at least one of the populations studied. The 90-plex MH panel enables effective differentiation of population groupings for major biogeographic regions as well as delineation of distinct subgroupings within regions. Open-source, web-based software is available to support validation of this technology for forensic case work analysis and to tailor MH analysis for specific geographical regions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00439-021-02382-0. Springer Berlin Heidelberg 2021-10-13 2021 /pmc/articles/PMC8553733/ /pubmed/34643790 http://dx.doi.org/10.1007/s00439-021-02382-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Investigation Pakstis, Andrew J. Gandotra, Neeru Speed, William C. Murtha, Michael Scharfe, Curt Kidd, Kenneth K. The population genetics characteristics of a 90 locus panel of microhaplotypes |
title | The population genetics characteristics of a 90 locus panel of microhaplotypes |
title_full | The population genetics characteristics of a 90 locus panel of microhaplotypes |
title_fullStr | The population genetics characteristics of a 90 locus panel of microhaplotypes |
title_full_unstemmed | The population genetics characteristics of a 90 locus panel of microhaplotypes |
title_short | The population genetics characteristics of a 90 locus panel of microhaplotypes |
title_sort | population genetics characteristics of a 90 locus panel of microhaplotypes |
topic | Original Investigation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8553733/ https://www.ncbi.nlm.nih.gov/pubmed/34643790 http://dx.doi.org/10.1007/s00439-021-02382-0 |
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