Evidence map›Paper›PMID 41081927›Full record

ArticleInternational journal of legal medicine2026

The potential of mRNA markers in body fluids and personal source analysis based on the QNome nanopore sequencing.

Suyu Li, Haowen Song, Jing Liu, Liu Qin, Mengyao Zhao, Yiping Hou, Bin Cong, Zheng Wang

Abstract read
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In one paragraph

Article in International journal of legal medicine, 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

8 authors.

Suyu Li *Institute of Forensic Medicine, West China School of Basic Medical Sciences & Forensic Medicine, Sichuan University, Chengdu, 610041, China.
Haowen Song *Institute of Forensic Medicine, West China School of Basic Medical Sciences & Forensic Medicine, Sichuan University, Chengdu, 610041, China.
Jing Liu *Institute of Forensic Medicine, West China School of Basic Medical Sciences & Forensic Medicine, Sichuan University, Chengdu, 610041, China.
Liu QinQitan Technology Ltd, Chengdu, Chengdu, 610044, China.
Mengyao ZhaoInstitute of Forensic Medicine, West China School of Basic Medical Sciences & Forensic Medicine, Sichuan University, Chengdu, 610041, China.
Yiping HouInstitute of Forensic Medicine, West China School of Basic Medical Sciences & Forensic Medicine, Sichuan University, Chengdu, 610041, China.
Bin CongCollege of Forensic Medicine, Hebei Key Laboratory of Forensic Medicine, Hebei Medical University, Shijiazhuang, 050017, China. hbydbincong@126.com.
Zheng WangInstitute of Forensic Medicine, West China School of Basic Medical Sciences & Forensic Medicine, Sichuan University, Chengdu, 610041, China. wangzhengtim@scu.edu.cn.ORCID http://orcid.org/0000-0003-3419-1741

Funding

the Major Program of National Natural Science Foundation of China 82293650the Major Program of National Natural Science Foundation of China 82293653
6 · The paper itself

Abstract

In forensic casework, unraveling the criminal nature of an event requires not only identifying the individual source of specific biological stains but also confirming their cellular origin. Recent studies have demonstrated the feasibility of identifying body fluids using specific mRNA markers and linking body fluids to their donors via coding region SNPs (cSNPs) within these mRNAs. Nanopore sequencing enables the detection of more cSNPs within longer mRNA amplicons due to its long-read capability. In this proof-of-principle study, we developed a targeted mRNA nanopore sequencing panel to simultaneously infer body fluid sources and identify individuals. This panel includes 12 body fluid-specific mRNAs and two reference genes (RGs), with a total of 41 cSNPs included in these 14 mRNA transcripts. Sequencing data showed that specific mRNAs were highly expressed in peripheral blood, semen, and menstrual blood, with an average read proportion exceeding 95% (excluding RGs reads). Cross-reactivity was observed in saliva and vaginal secretions, but all body fluid samples could still be accurately clustered. Alternative alleles were detected for 16 cSNPs, and genotyping results for randomly selected samples were validated for consistency with Sanger sequencing. The system demonstrated discriminatory power (DP) ranging from 0.5645 to 0.9017, providing information about the body fluid donor. However, further research is needed to identify more specific mRNAs, introduce additional highly polymorphic cSNPs, and perform evaluations on larger populations.

Indexed as

Body FluidsNanopore SequencingPolymorphism, Single NucleotideRNA, MessengerCervix MucusFemaleForensic GeneticsGenetic MarkersGenotypeHumansMaleMenstruationProof of Concept StudySalivaSemenGenetic MarkersRNA, MessengerBody fluid identificationCoding single nucleotide polymorphism (cSNP)Forensic geneticsMRNANanopore sequencing

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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.