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Genetic Identification of Burned Human Remains: A Systematic Review.

Background/Objectives: DNA-based identification of degraded human remains represents a major challenge in forensic science, particularly in cases involving burned, fragmented, or commingled bodies. Advances in forensic genetics have expanded the analytical capabilities for such samples; however, the effectiveness of different approaches and their integration within Disaster Victim Identification (DVI) workflows remain heterogeneous. This systematic review aims to critically evaluate current evidence on DNA-based identification of degraded remains, focusing on methodological strategies, emerging genomic technologies, and DVI applications, while integrating laboratory evidence and operational forensic practice into a structured analytical framework. Methods: A systematic literature search was conducted in Scopus and Web of Science from database inception to 5 June 2026, following PRISMA 2020 guidelines. Eligible studies included original research addressing DNA analysis of degraded, thermally altered, or highly compromised human remains in forensic or DVI contexts. After a multistep screening process involving title/abstract and full-text evaluation, 37 studies were included. Data were extracted and organized into three thematic categories: (i) core DNA analysis, (ii) advanced molecular technologies, and (iii) DVI case applications. Results: The findings demonstrate that DNA recovery from degraded remains is influenced by thermal exposure, tissue type, and sampling strategy. Teeth and dense cortical bone consistently provide higher DNA yield. While autosomal STR profiling remains the primary analytical approach, its limitations in highly degraded samples are mitigated through the complementary use of mitochondrial DNA (mtDNA), Y-chromosome STRs (Y-STRs), and SNP markers, together with advanced sequencing technologies such as massively parallel sequencing (MPS). Emerging technologies, including rapid DNA systems and predictive models based on macroscopic indicators, significantly enhance efficiency and success rates. DVI studies report identification rates exceeding 90-95% when multidisciplinary and structured workflows are applied. The evidence further supports a flexible triage-based analytical strategy, in which marker selection is guided by tissue preservation and degradation level. Conclusions: DNA-based identification of degraded human remains has evolved into an adaptive, multi-level forensic process. Successful outcomes rely on the integration of optimized sampling, hierarchical genetic analysis, and coordinated DVI strategies. The findings support a triage-based framework that links tissue selection, degradation assessment, and analytical methodology to maximize identification success. Future developments should focus on predictive models, advanced genomic tools, and standardized workflows to further improve identification in challenging forensic scenarios.

Humans

An avuncular relationship generating a parent-offspring signal in forensic familial DNA searching: a case report.

In 2019, a series of vehicle burglaries occurred near the Dead Sea, Israel. DNA profiles obtained from six crime scenes were concordant, but no direct match was found in the national forensic DNA database. A CODIS familial search identified a male candidate as the highest-ranked potential relative. Pairwise kinship analysis based on 15 shared autosomal STR loci yielded the highest likelihood ratio under the parent-offspring (PO) hypothesis (LR = 530,300). However, Y-STR analysis performed in parallel with the familial search excluded a shared paternal lineage. Full mitochondrial genome sequencing subsequently demonstrated an identical haplotype, supporting a shared maternal lineage. Investigative inquiries identified a maternal uncle of the candidate whose reference STR profile fully matched the evidentiary profile.Population-based simulations of 100,000 second-degree relative pairs and 100,000 unrelated pairs showed that 2.05% of simulated second-degree pairs produced LRs equal to or greater than the observed second-degree LR (CODIS HS LR = 5,538), demonstrating that the observed similarity, although within the upper tail, remained within the expected second-degree distribution. In a retrospective expanded-marker analysis, increasing the shared autosomal STR loci from 15 to 20 excluded the PO hypothesis (LR = 0), while close-relationship hypotheses remained supported.This case illustrates how stochastic allele sharing across a limited number of autosomal STR loci can produce overlap between relationship categories and how additional markers can substantially alter relationship inference. Integrating sufficiently informative autosomal markers, lineage-specific markers, statistical evaluation, and investigative information is therefore important when interpreting familial DNA search results.

Autosomal STRs