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MicroHapDB: A Portable and Extensible Database of All Published Microhaplotype Marker and Frequency Data
Microhaplotypes are the subject of significant interest in the forensics community as a promising multi-purpose forensic DNA marker for human identification. Microhaplotype markers are composed of multiple SNPs in close proximity, such that a single NGS read can simultaneously genotype the individua...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7427474/ https://www.ncbi.nlm.nih.gov/pubmed/32849792 http://dx.doi.org/10.3389/fgene.2020.00781 |
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author | Standage, Daniel S. Mitchell, Rebecca N. |
author_facet | Standage, Daniel S. Mitchell, Rebecca N. |
author_sort | Standage, Daniel S. |
collection | PubMed |
description | Microhaplotypes are the subject of significant interest in the forensics community as a promising multi-purpose forensic DNA marker for human identification. Microhaplotype markers are composed of multiple SNPs in close proximity, such that a single NGS read can simultaneously genotype the individual SNPs and phase them in aggregate to determine the associated donor haplotype. Abundant throughout the human genome, numerous recent studies have sought to discover and rank microhaplotype markers according to allelic diversity within and among populations. Microhaplotypes provide an appealing alternative to STR markers for human identification and mixture deconvolution, but can also be optimized for ancestry inference or combined with phenotype SNPs for prediction of externally visible characteristics in a multiplex NGS assay. Designing and evaluating panels of microhaplotypes is complicated by the lack of a convenient database of all published data, as well as the lack of population allele frequency data spanning disparate marker collections. We present MicroHapDB, a comprehensive database of published microhaplotype marker and frequency data, as a tool to advance the development of microhaplotype-based human forensics capabilities. We also present population allele frequencies derived from 26 global population samples for all microhaplotype markers published to date, facilitating the design and interpretation of custom multi-source panels. We submit MicroHapDB as a resource for community members engaged in marker discovery, population studies, assay development, and panel and kit design. |
format | Online Article Text |
id | pubmed-7427474 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-74274742020-08-25 MicroHapDB: A Portable and Extensible Database of All Published Microhaplotype Marker and Frequency Data Standage, Daniel S. Mitchell, Rebecca N. Front Genet Genetics Microhaplotypes are the subject of significant interest in the forensics community as a promising multi-purpose forensic DNA marker for human identification. Microhaplotype markers are composed of multiple SNPs in close proximity, such that a single NGS read can simultaneously genotype the individual SNPs and phase them in aggregate to determine the associated donor haplotype. Abundant throughout the human genome, numerous recent studies have sought to discover and rank microhaplotype markers according to allelic diversity within and among populations. Microhaplotypes provide an appealing alternative to STR markers for human identification and mixture deconvolution, but can also be optimized for ancestry inference or combined with phenotype SNPs for prediction of externally visible characteristics in a multiplex NGS assay. Designing and evaluating panels of microhaplotypes is complicated by the lack of a convenient database of all published data, as well as the lack of population allele frequency data spanning disparate marker collections. We present MicroHapDB, a comprehensive database of published microhaplotype marker and frequency data, as a tool to advance the development of microhaplotype-based human forensics capabilities. We also present population allele frequencies derived from 26 global population samples for all microhaplotype markers published to date, facilitating the design and interpretation of custom multi-source panels. We submit MicroHapDB as a resource for community members engaged in marker discovery, population studies, assay development, and panel and kit design. Frontiers Media S.A. 2020-08-07 /pmc/articles/PMC7427474/ /pubmed/32849792 http://dx.doi.org/10.3389/fgene.2020.00781 Text en Copyright © 2020 Standage and Mitchell. 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 Standage, Daniel S. Mitchell, Rebecca N. MicroHapDB: A Portable and Extensible Database of All Published Microhaplotype Marker and Frequency Data |
title | MicroHapDB: A Portable and Extensible Database of All Published Microhaplotype Marker and Frequency Data |
title_full | MicroHapDB: A Portable and Extensible Database of All Published Microhaplotype Marker and Frequency Data |
title_fullStr | MicroHapDB: A Portable and Extensible Database of All Published Microhaplotype Marker and Frequency Data |
title_full_unstemmed | MicroHapDB: A Portable and Extensible Database of All Published Microhaplotype Marker and Frequency Data |
title_short | MicroHapDB: A Portable and Extensible Database of All Published Microhaplotype Marker and Frequency Data |
title_sort | microhapdb: a portable and extensible database of all published microhaplotype marker and frequency data |
topic | Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7427474/ https://www.ncbi.nlm.nih.gov/pubmed/32849792 http://dx.doi.org/10.3389/fgene.2020.00781 |
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