Evidence map›Paper›PMID 41143891›Full record

ArticleHuman genetics2025

Development and validation of an MPS-based 513-Plex SNP identity panel for degraded forensic samples.

Linyu Shi, Xiaoxiao Feng, Mengyang Zhao, Anjie Wei, Jiarong Zhang, Piao Yuan, Haoliang Fan, Jiangwei Yan

Abstract readValidation Study
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In one paragraph

Article in Human genetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Linyu ShiSchool of Forensic Medicine, Shanxi Medical University, Jinzhong, 030600, Shanxi, China.
Xiaoxiao FengSchool of Forensic Medicine, Shanxi Medical University, Jinzhong, 030600, Shanxi, China.
Mengyang ZhaoSchool of Forensic Medicine, Shanxi Medical University, Jinzhong, 030600, Shanxi, China.
Anjie WeiSchool of Forensic Medicine, Shanxi Medical University, Jinzhong, 030600, Shanxi, China.
Jiarong ZhangSchool of Forensic Medicine, Shanxi Medical University, Jinzhong, 030600, Shanxi, China.
Piao YuanSchool of Forensic Medicine, Shanxi Medical University, Jinzhong, 030600, Shanxi, China.
Haoliang FanSchool of Forensic Medicine, Shanxi Medical University, Jinzhong, 030600, Shanxi, China. fanhaoliang198931@163.com.
Jiangwei YanSchool of Forensic Medicine, Shanxi Medical University, Jinzhong, 030600, Shanxi, China. yanjw@sxmu.edu.cn.

Funding

Doctoral Foundation Program of Shanxi Province SD2327National Key Research and Development Program of China 2023YFF0614601-2National Natural Science Foundation of China Nos.82030058Natural Science Foundation of Shanxi Province of China 202303021212124Scientific and Technological Innovation Programs of Higher Education Institutions in Shanxi 2023L062
6 · The paper itself

Abstract

Degraded samples pose a challenge in routine forensic practice. The commonly used short tandem repeat markers are not optimally suitable for the analysis of degraded samples because of their structural complexity and locus length. By contrast, single nucleotide polymorphisms (SNPs), characterised by their single base mutation feature, enable the design of short amplification fragments, conferring an advantage in detecting mutations in degraded samples. Hence, our team has developed a multiplex amplification system for individual identification of degraded samples, encompassing 507 autosomal SNP loci, five Y-InDel loci, and one amelogenin sex determination locus. The amplification fragment lengths in this multiplex system range from 81 to 116 bp. The forensic applicability of this panel was validated through sequencing analysis of 201 samples. Among these were 30 degraded samples (simulated degraded samples: heat degradation and ultrasonic fragmentation; formalin-fixed, paraffin-embedded samples). The results indicated that the genotyping accuracy of all loci included in this panel remained at 100% for samples with 0.1 ng of DNA input and severe degradation. Sensitivity experiments revealed that at a DNA input of only 31.25 pg, the locus detection rate reached 100%, with genotype accuracy of 92.5%. Based on population data analysis, the total discrimination power of this system reached 1-5.513 × 10

Indexed as

Forensic GeneticsHigh-Throughput Nucleotide SequencingPolymorphism, Single NucleotideAmelogeninChromosomes, Human, YDNA Degradation, NecroticFemaleGenotypeHumansMaleMicrosatellite RepeatsMultiplex Polymerase Chain ReactionAmelogeninDegraded DNAIndividual identificationMassively parallel sequencingSingle nucleotide polymorphismValidation methodology

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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.