Resolution of mitochondrial DNA mixtures using a probe capture next generation sequencing system and phylogenetic-based software.


Journal

Forensic science international. Genetics
ISSN: 1878-0326
Titre abrégé: Forensic Sci Int Genet
Pays: Netherlands
ID NLM: 101317016

Informations de publication

Date de publication:
07 2021
Historique:
received: 30 01 2021
revised: 27 04 2021
accepted: 07 05 2021
pubmed: 31 5 2021
medline: 18 8 2021
entrez: 30 5 2021
Statut: ppublish

Résumé

Interpreting mixtures with nuclear genetic markers remains one of the persisting challenges in forensic DNA analysis, particularly when the DNA is degraded or present in trace amounts. In these scenarios, analyzing mitochondrial (mt) DNA can be useful due to the higher copy number per cell compared to nuclear DNA. However, until the emergence of Next-Generation Sequencing (NGS) with its clonal sequencing capability, analysis of mtDNA mixtures was very challenging. A mitochondrial genome probe capture Next-Generation Sequencing (NGS) system was used to sequence complex mtDNA mixtures and two different software programs to analyze the sequence data. Analysis of contrived mixtures of two contributors in 50:50 and 95:5 ratios as well as three-person mixtures ranging from near equal proportions (~33:33:33 ratio) to low amounts of the minor contributors (e.g., a 90:5:5 ratio) is reported. This system was also applied to the analysis of mtDNA mixtures from forensically relevant samples. For data analysis, both the variant frequency-based software program GeneMarker®HTS and the phylogenetic-based software program Mixemt was used to de-convolute the mixtures. Using the massively parallel, clonal features of NGS, one can bioinformatically separate and count the individual sequence reads to calculate the proportions of individual contributors using phylogenetically informative polymorphisms. GeneMarker®HTS allows us to detect all mutations, including "private" mutations (non-phylogenetically informative polymorphisms) and assign them to individual contributors based on the frequency of the sequence reads, provided that the proportions of the various contributors are sufficiently different. Using a probe capture NGS system and both GeneMarker®HTS and Mixemt software programs, the interpretation of complex mixtures of equal proportion contributors, trace amount contributors, and more than two contributors in contrived mixtures, as well as interpretation of challenging forensic specimens is demonstrated.

Identifiants

pubmed: 34052577
pii: S1872-4973(21)00069-7
doi: 10.1016/j.fsigen.2021.102531
pii:
doi:

Substances chimiques

DNA, Mitochondrial 0

Types de publication

Journal Article Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

102531

Informations de copyright

Copyright © 2021 Elsevier B.V. All rights reserved.

Auteurs

Mary Wisner (M)

Forensic Science Graduate Program, University of California-Davis, 1909 Galileo Ct. Ste. B, Davis, CA, USA.

Henry Erlich (H)

Children's Hospital Oakland Research Institute (CHORI), 5700 M.L.K. Jr. Way, Oakland, CA, USA.

Shelly Shih (S)

Children's Hospital Oakland Research Institute (CHORI), 5700 M.L.K. Jr. Way, Oakland, CA, USA.

Cassandra Calloway (C)

Children's Hospital Oakland Research Institute (CHORI), 5700 M.L.K. Jr. Way, Oakland, CA, USA. Electronic address: Sandycalloway@yahoo.com.

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Classifications MeSH