Evidence map›Paper›PMID 41148463›Full record

ReviewForensic science, medicine, and pathology2026

Forensic applications of rapidly mutating Y-STR markers: current status and future perspectives.

Sunganani Ndomondo, Sreekutti S, Paheli Sharma, Vishal Mevada

Abstract readReview
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In one paragraph

Review in Forensic science, medicine, and pathology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Sunganani NdomondoSchool of Forensic Science, National Forensic Sciences University, Gandhinagar, 382007, Gujarat, India.ORCID http://orcid.org/0009-0000-6298-1391
Sreekutti SSchool of Forensic Science, National Forensic Sciences University, Gandhinagar, 382007, Gujarat, India.ORCID http://orcid.org/0009-0005-1196-5013
Paheli SharmaSchool of Forensic Science, National Forensic Sciences University, Gandhinagar, 382007, Gujarat, India.ORCID http://orcid.org/0009-0005-4061-9304
Vishal MevadaSchool of Forensic Science, National Forensic Sciences University, Gandhinagar, 382007, Gujarat, India. vmevada102@gmail.com.ORCID http://orcid.org/0000-0003-0739-026X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Over the past few years, the Y chromosome has emerged as a crucial investigative tool, gaining significant applications in multiple disciplines such as forensics, anthropology, and genetics. Standard Y-STRs are particularly useful for identifying male donors in mixed deoxyribonucleic acid (DNA) samples dominated by female DNA, in tracing male patrilineal lineage, and in disaster victim identification. Nonetheless, their limited ability to distinguish closely related males has constrained their forensic utility. Evidence from multiple studies shows that rapidly mutating (RM) Y-STR markers improve male differentiation owing to their elevated mutation rates. Recent advances in RM Y-STR research include marker discovery, panel validation, and development of multiplex assays. RM Y-STRs have demonstrated effectiveness in male relative differentiation, kinship analysis, and analysis of complex mixtures with multiple contributors. Beyond forensic casework, RM Y-STRs hold promise in clinical contexts, particularly in investigating unexplained infertility and assessing reproductive risks. The advanced genotyping approaches, such as capillary electrophoresis, massively parallel sequencing (MPS), and the use of advanced computational analytical methods, have further enhanced their utility. Nevertheless, their implementation is complicated by interpretive challenges and inconsistencies in mutation rates across populations. Addressing these challenges through further research on additional RM Y-STRs, establishing standardised methods for determining mutation rates, and expanding databases like the Y chromosome Haplotype Reference Database (YHRD) to include RM Y-STR markers is crucial to fully leverage the potential of RM Y-STR markers.

Indexed as

Chromosomes, Human, YForensic GeneticsMicrosatellite RepeatsMutationDNA FingerprintingElectrophoresis, CapillaryGenetic MarkersHigh-Throughput Nucleotide SequencingHumansMaleMutation RateGenetic MarkersRapidly Mutating Y-STR (RM Y-STR) markersShort Tandem Repeats (STRs)Y-chromosomeY-STRs

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.