Evidence map›Paper›PMID 39661160›Full record

ArticleInternational journal of legal medicine2025

Complex kinship testing using the MGIEasy Pa-SNPs genotyping kit.

Qingzhen Zhang, Tingting Dong, Xueqian Wang, Xiaochang Zhang, Sen Yang, Peng Cheng, Zhe Zhou, Shengqi Wang

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Article in International journal of legal medicine, 2025. 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
–field-weighted citation impact
1 · What the graph read from it

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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.

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3 · Its place in the literature

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3 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.

Qingzhen Zhang *Bioinformatics center of AMMS, Beijing, P. R. China.
Tingting Dong *Bioinformatics center of AMMS, Beijing, P. R. China.
Xueqian WangBioinformatics center of AMMS, Beijing, P. R. China.
Xiaochang ZhangBioinformatics center of AMMS, Beijing, P. R. China.
Sen YangBioinformatics center of AMMS, Beijing, P. R. China.
Peng ChengBioinformatics center of AMMS, Beijing, P. R. China.
Zhe ZhouBioinformatics center of AMMS, Beijing, P. R. China. zhouzhe@bmi.ac.cn.ORCID http://orcid.org/0000-0003-4616-0467
Shengqi WangBioinformatics center of AMMS, Beijing, P. R. China. sqwang@bmi.ac.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Disaster victim identification and criminal investigations have intensified the demand of complex kinship testing. Compared to close relatives, distant relatives share fewer identical-by-descent genetic segments; therefore, more genetic markers are required to improve the system effectiveness. Driven by the progress of next-generation sequencing, several commercial or in-house panels, including a large number of genetic markers, have been developed and applied in forensic caseworks. However, few efficient panels are available for first cousins (FC) kinship testing. Here, we adopted the MGIEasy Pa-SNPs genotyping kit, a two-step multiplex PCR strategy to detect 2,009 SNPs, and evaluated their system effectiveness in complex kinship analysis. Samples from 10,000 pairs of relatives and unrelated individuals were simulated to evaluate the system power. Simultaneously, real samples were used to further confirm this, including 72 pairs of full siblings (FS), 52 pairs of uncle/aunt/-niece/nephew (UN), 92 pairs of FC, 79 pairs of first cousin once removed (1C1R), and 780 pairs of unrelated individuals. The results showed that this kit was sufficiently powerful in FS, UN, and FC versus unrelated kinship testing and could also discriminate part of 1C1R relatives against unrelated individuals. This method was also powerful in the kinship determination of FS versus UN, FS versus FC, FS versus 1C1R, and UN versus 1C1R kinship testing but had limited power to determine UN versus FC and FC versus 1C1R relationships. This study provides an effective strategy and guidance for complex kinship analysis in forensic practice.

Indexed as

Genotyping TechniquesMultiplex Polymerase Chain ReactionPedigreePolymorphism, Single NucleotideDNA FingerprintingFamilyFemaleForensic GeneticsGenetic MarkersGenotypeHumansMaleGenetic MarkersComplex kinship testingNext generation sequencingSNPsSystem effectiveness

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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.