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Short tandem repeats of the nuclear genome have been the preferred markers for analyzing forensic DNA mixtures. However, when nuclear DNA in a sample is degraded or limited, mitochondrial DNA (mtDNA) markers provide a powerful alternative. Though historically considered challenging, the interpretation and analysis of mtDNA mixtures have recently seen renewed interest with the advent of massively parallel sequencing. However, there are only a few software tools available for mtDNA mixture interpretation. To address this gap, the Mitochondrial Mixture Deconvolution and Interpretation Tool (MMDIT) was developed. MMDIT is an interactive application complete with a graphical user interface that allows users to deconvolve mtDNA (whole or partial genomes) mixtures into constituent donor haplotypes and estimate random match probabilities on these resultant haplotypes. In cases where deconvolution might not be feasible, the software allows mixture analysis directly within a binary framework (i.e. qualitatively, only using data on allele presence/absence). This paper explains the functionality of MMDIT, using an example of an in vitro two-person mtDNA mixture with a ratio of 1:4. The uniqueness of MMDIT lies in its ability to resolve mixtures into complete donor haplotypes using a statistical phasing framework before mixture analysis and evaluating statistical weights employing a novel graph algorithm approach. MMDIT is the first available open-source software that can automate mtDNA mixture deconvolution and analysis. The MMDIT web application can be accessed online at https://www.unthsc.edu/mmdit/. The source code is available at https://github.com/SammedMandape/MMDIT_UI and archived on zenodo (https://doi.org/10.5281/zenodo.4770184).
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http://dx.doi.org/10.1016/j.fsigen.2021.102568 | DOI Listing |
Pharmacol Rep
September 2025
Faculty of Pharmaceutical Sciences in Sosnowiec, Department of Pharmaceutical Chemistry, Medical University of Silesia, Jagiellońska 4, Sosnowiec, 41-200, Poland.
Background: Triple-negative breast cancer (TNBC) is characterized by high invasiveness, high metastatic potential, and poor prognosis. TNBC is not sensitive to endocrine therapy or HER2-targeted treatment, highlighting the need for the development of standardized TNBC treatment regimens. Thus, the development of new TNBC treatment strategies has become an urgent need.
View Article and Find Full Text PDFBMC Genomics
August 2025
Toyota Central R&D Labs., Inc. Nagakute, Aichi, 480-1192, Japan.
Background: Mitochondrial DNA sequences are used for inter- and intra-specific comparison analysis in ecological studies. Instead of using short regions as marker sequences, analyzing longer regions, such as whole mitochondrial DNA sequences, can improve the accuracy of such studies by increasing the likelihood of detecting species or specific sequences. However, current methods for sequencing whole mitochondrial DNA require primer design for each target species or long fragments of genomic DNA as a PCR template.
View Article and Find Full Text PDFEnviron Res
August 2025
Department of Environmental Health Sciences, Mailman School of Public Health, Columbia University, New York, NY, USA.
Background: Phthalates, a group of endocrine disrupting chemicals used in plastics, are ubiquitous in the environment and may influence cellular processes related to child health and development. Mitochondrial DNA copy number (mtDNAcn), telomere length (TL), and DNA methylation-based epigenetic gestational age acceleration (EGAA) are accessible biomarkers associated with biological aging and development. Little is known about how gestational phthalate exposure, individually and in mixtures, may impact biomarkers of biological aging through childhood.
View Article and Find Full Text PDFForensic Sci Int Genet
January 2026
Institute of Legal Medicine, University of Münster, Röntgenstr. 23, Münster 48149, Germany. Electronic address:
TrACE (Trace Analysis Collaborative Exercise) represents a novel, strictly expert driven and transparent concept of external quality control based on a combination of proficiency testing and interlaboratory comparisons. TrACE is an official proficiency test scheme of the German Stain Commission and acts in accordance with the recommendations for proficiency testing issued by this commission and outlined in DIN EN ISO 17025. TrACE offers modules on all aspects of forensic genetics that address challenges encountered in real casework.
View Article and Find Full Text PDFDNA Repair (Amst)
August 2025
Department of Pharmacology and Toxicology, Institute for Nutrition and Translational Research in Metabolism (NUTRIM), Maastricht University, Maastricht 6229 ER, the Netherlands. Electronic address:
Animal models suggest an association between base excision repair (BER) deficiency and increased risk of obesity. To mechanistically investigate the effect of BER deficiency on intracellular lipid accumulation, we studied metabolic activity in in vitro BER knockdown (KD) models, targeting MutY DNA Glycosylase (MUTYH), Nth Like DNA Glycosylase 1 (NTHL1) and 8-Oxoguanine DNA Glycosylase (OGG1). We hypothesized that exposing BER deficient cells to lipids leads to reduced mitochondrial function and enhanced intracellular lipid accumulation.
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