Floor Claessens , Mikkel Meyer Andersen , Christina Amory , Cristina Arévalo , Stijn Desmyter , Sophie Dognaux , Kristiaan J. van der Gaag , Tomasz Grzybowski , Gabriela Huber , Filomena Melchionda , Hiroaki Nakanishi , Tóra Olsen , Cristina Pie , Lourdes Prieto , Katarzyna Skonieczna , Chiara Turchi , Walther Parson , Vania Pereira
{"title":"MitoMetrics: Incorporation of mtDNA profile discrepancies in likelihood ratio calculations","authors":"Floor Claessens , Mikkel Meyer Andersen , Christina Amory , Cristina Arévalo , Stijn Desmyter , Sophie Dognaux , Kristiaan J. van der Gaag , Tomasz Grzybowski , Gabriela Huber , Filomena Melchionda , Hiroaki Nakanishi , Tóra Olsen , Cristina Pie , Lourdes Prieto , Katarzyna Skonieczna , Chiara Turchi , Walther Parson , Vania Pereira","doi":"10.1016/j.fsigen.2026.103477","DOIUrl":null,"url":null,"abstract":"<div><div>Interpretation of mitochondrial DNA (mtDNA) evidence in a forensic context faces challenges, particularly when evaluating mtDNA profiles from different tissues. In hair, for example, the segregation of mtDNA shows tight bottlenecks that can result in different mtDNA profiles between and along hair shafts, and between hair and other reference tissues of the same donor. Current forensic interpretation guidelines for mtDNA are based on conventions on the number of discrepant positions observed between the two compared profiles. Most legislations consider two discrepancies between samples as an exclusion, and one discrepancy as an inclusion or as an inconclusive result. More data are needed to understand the variation and occurrence of discrepancies in samples from the same donor, to be able to incorporate this knowledge into a mathematical approach that effectively quantifies the probability of these events. This study reports the first project of the MitoMetrics collaborative initiative. In this study, data were generated from several participating laboratories, and previously published data, along with data generated from casework. mtDNA profiles from blood/buccal reference samples were compared to those from hair shafts from the same individuals. Results report the levels of heteroplasmy detected in the different tissues, the number of differences observed between the tissue comparisons, and the number of discrepant positions observed. We suggest a preliminary model for calculating the evidential value of mtDNA-based evidence using a likelihood ratio approach, that takes into consideration the occurrence of discrepancies between profiles from the same donor. This work represents the first attempt to quantify the probability of finding discrepant events between tissues and to incorporate these when reporting mtDNA in a forensic context.</div></div>","PeriodicalId":50435,"journal":{"name":"Forensic Science International-Genetics","volume":"84 ","pages":"Article 103477"},"PeriodicalIF":3.6000,"publicationDate":"2026-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Forensic Science International-Genetics","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S187249732600058X","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/3/1 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 0
Abstract
Interpretation of mitochondrial DNA (mtDNA) evidence in a forensic context faces challenges, particularly when evaluating mtDNA profiles from different tissues. In hair, for example, the segregation of mtDNA shows tight bottlenecks that can result in different mtDNA profiles between and along hair shafts, and between hair and other reference tissues of the same donor. Current forensic interpretation guidelines for mtDNA are based on conventions on the number of discrepant positions observed between the two compared profiles. Most legislations consider two discrepancies between samples as an exclusion, and one discrepancy as an inclusion or as an inconclusive result. More data are needed to understand the variation and occurrence of discrepancies in samples from the same donor, to be able to incorporate this knowledge into a mathematical approach that effectively quantifies the probability of these events. This study reports the first project of the MitoMetrics collaborative initiative. In this study, data were generated from several participating laboratories, and previously published data, along with data generated from casework. mtDNA profiles from blood/buccal reference samples were compared to those from hair shafts from the same individuals. Results report the levels of heteroplasmy detected in the different tissues, the number of differences observed between the tissue comparisons, and the number of discrepant positions observed. We suggest a preliminary model for calculating the evidential value of mtDNA-based evidence using a likelihood ratio approach, that takes into consideration the occurrence of discrepancies between profiles from the same donor. This work represents the first attempt to quantify the probability of finding discrepant events between tissues and to incorporate these when reporting mtDNA in a forensic context.
期刊介绍:
Forensic Science International: Genetics is the premier journal in the field of Forensic Genetics. This branch of Forensic Science can be defined as the application of genetics to human and non-human material (in the sense of a science with the purpose of studying inherited characteristics for the analysis of inter- and intra-specific variations in populations) for the resolution of legal conflicts.
The scope of the journal includes:
Forensic applications of human polymorphism.
Testing of paternity and other family relationships, immigration cases, typing of biological stains and tissues from criminal casework, identification of human remains by DNA testing methodologies.
Description of human polymorphisms of forensic interest, with special interest in DNA polymorphisms.
Autosomal DNA polymorphisms, mini- and microsatellites (or short tandem repeats, STRs), single nucleotide polymorphisms (SNPs), X and Y chromosome polymorphisms, mtDNA polymorphisms, and any other type of DNA variation with potential forensic applications.
Non-human DNA polymorphisms for crime scene investigation.
Population genetics of human polymorphisms of forensic interest.
Population data, especially from DNA polymorphisms of interest for the solution of forensic problems.
DNA typing methodologies and strategies.
Biostatistical methods in forensic genetics.
Evaluation of DNA evidence in forensic problems (such as paternity or immigration cases, criminal casework, identification), classical and new statistical approaches.
Standards in forensic genetics.
Recommendations of regulatory bodies concerning methods, markers, interpretation or strategies or proposals for procedural or technical standards.
Quality control.
Quality control and quality assurance strategies, proficiency testing for DNA typing methodologies.
Criminal DNA databases.
Technical, legal and statistical issues.
General ethical and legal issues related to forensic genetics.