Evidence map›Paper›PMID 41407971›Full record

ArticleInternational journal of legal medicine2026

Development and validation of a STR and SNP multiplex detection system (88 STRs and 348 SNPs) using massively parallel sequencing.

Yanfang Lu, Fan Yang, Yanan Liu, Yujia Xuan, Jinyuan Zhao, Mengxiao Liao, Yu Xing, Sitong Liu, Suhua Zhang, Anqi Chen

Abstract readValidation Study
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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 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Yanfang Lu *Institute of Forensic Science, Fudan University, Shanghai, 200032, China.
Fan Yang *Key Laboratory of Forensic Evidence and Science Technology, Institute of Forensic Science, Ministry of Public Security, Shanghai, 200042, China.
Yanan LiuKey Laboratory of Forensic Evidence and Science Technology, Institute of Forensic Science, Ministry of Public Security, Shanghai, 200042, China.
Yujia XuanInstitute of Forensic Science, Fudan University, Shanghai, 200032, China.
Jinyuan ZhaoInstitute of Forensic Science, Fudan University, Shanghai, 200032, China.
Mengxiao LiaoInstitute of Forensic Science, Fudan University, Shanghai, 200032, China.
Yu XingInstitute of Forensic Science, Fudan University, Shanghai, 200032, China.
Sitong LiuInstitute of Forensic Science, Fudan University, Shanghai, 200032, China.
Suhua ZhangInstitute of Forensic Science, Fudan University, Shanghai, 200032, China. zhang_suhua@fudan.edu.cn.
Anqi ChenInstitute of Forensic Science, Fudan University, Shanghai, 200032, China. anqi_chen@fudan.edu.cn.

Funding

National Key R&D Program of China 2024YFC3306702National Natural Science Foundation of China 82302124
6 · The paper itself

Abstract

Short tandem repeats (STRs) have long been the gold standard in forensic DNA analysis, while single nucleotide polymorphisms (SNPs) have increasingly emerged as valuable complementary markers. The advent of massively parallel sequencing (MPS) technology has significantly enhanced the detection resolution of both STRs and SNPs, providing novel approaches for forensic human identification. In this study, we developed and validated a comprehensive multiplex detection system utilizing MPS technology, which enabled the concurrent analyses of 88 STRs and 348 SNPs. Following the SWGDAM guidelines, validation studies were conducted to assess the forensic applicability of the system. Sensitivity study revealed that 100% STR profiles could be obtained from ≥ 0.125 ng, and 100% SNP profiles were achieved with ≥ 0.0625 ng. The panel showed high accuracy, achieving a 99.78% concordance rate with conventional capillary electrophoresis (CE) DNA profiles. The system exhibited robust performance in the presence of four common PCR inhibitors (including humic acid, melanin, indigo, and hematin). Additionally, 99.42% of STR genotypes and 100% of SNP genotypes were successfully obtained from degraded DNA shorter than 500 bp. Furthermore, across gender combinations in mixed samples, both STR and SNP markers performed robustly at 1:1 and 1:3 ratios. At extreme proportions, male-female mixtures (99:1) enable the detection of scarce minor contributors at Y-STR loci. For SNP loci, the ACR value serves as a key evaluative metric for distinguishing mixtures. ROC analysis of these SNP data yielded an AUC of 0.909. Population genetics analyses revealed that the cumulative power of discrimination (CPD) and cumulative probability of exclusion (CPE) both exceeded 0.999999, highlighting its extensive applicability and practical value in forensic genetics. This comprehensive validation study confirmed that the multiplex panel provided high sensitivity, accuracy, and reliability, representing a significant advancement in forensic DNA analysis methodology.

Indexed as

DNA FingerprintingHigh-Throughput Nucleotide SequencingMicrosatellite RepeatsPolymorphism, Single NucleotideSequence Analysis, DNADNA Degradation, NecroticElectrophoresis, CapillaryFemaleForensic GeneticsGenotypeHumansMaleMultiplex Polymerase Chain ReactionForensic geneticsMassively parallel sequencing (MPS)Short tandem repeat (STR)Single nucleotide polymorphism (SNP)SWGDAM validation

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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.