Evidence map›Paper›PMID 26297200›Full record

ArticleInternational journal of legal medicine2016

Genotyping of 75 SNPs using arrays for individual identification in five population groups.

Hsiao-Lin Hwa, Lawrence Shih Hsin Wu, Chun-Yen Lin, Tsun-Ying Huang, Hsiang-I Yin, Li-Hui Tseng, James Chun-I Lee

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Article in International journal of legal medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.0field-weighted citation impact, top 13% of its field
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

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3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 13 citations in OpenAlex.

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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

7 authors at 4 institutions in 1 country.

Hsiao-Lin HwaDepartment and Graduate Institute of Forensic Medicine, College of Medicine, National Taiwan University, Taipei, Taiwan, Republic of China.
Lawrence Shih Hsin WuInstitute of Medical Sciences, Tzu Chi University, Hualien, Taiwan, Republic of China.
Chun-Yen LinInstitute of Forensic Medicine, Ministry of Justice, Taipei, Taiwan, Republic of China.
Tsun-Ying HuangInstitute of Forensic Medicine, Ministry of Justice, Taipei, Taiwan, Republic of China.
Hsiang-I YinDepartment and Graduate Institute of Forensic Medicine, College of Medicine, National Taiwan University, Taipei, Taiwan, Republic of China.
Li-Hui TsengDepartment of Medical Genetics, National Taiwan University Hospital, Taipei, Taiwan, Republic of China.
James Chun-I LeeDepartment and Graduate Institute of Forensic Medicine, College of Medicine, National Taiwan University, Taipei, Taiwan, Republic of China. jimlee@ntu.edu.tw.
National Taiwan University · TWMinistry of Justice · TWNational Taiwan University Hospital · TWTzu Chi University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Single nucleotide polymorphism (SNP) typing offers promise to forensic genetics. Various strategies and panels for analyzing SNP markers for individual identification have been published. However, the best panels with fewer identity SNPs for all major population groups are still under discussion. This study aimed to find more autosomal SNPs with high heterozygosity for individual identification among Asian populations. Ninety-six autosomal SNPs of 502 DNA samples from unrelated individuals of five population groups (208 Taiwanese Han, 83 Filipinos, 62 Thais, 69 Indonesians, and 80 individuals with European, Near Eastern, or South Asian ancestry) were analyzed using arrays in an initial screening, and 75 SNPs (group A, 46 newly selected SNPs; groups B, 29 SNPs based on a previous SNP panel) were selected for further statistical analyses. Some SNPs with high heterozygosity from Asian populations were identified. The combined random match probability of the best 40 and 45 SNPs was between 3.16 × 10(-17) and 7.75 × 10(-17) and between 2.33 × 10(-19) and 7.00 × 10(-19), respectively, in all five populations. These loci offer comparable power to short tandem repeats (STRs) for routine forensic profiling. In this study, we demonstrated the population genetic characteristics and forensic parameters of 75 SNPs with high heterozygosity from five population groups. This SNPs panel can provide valuable genotypic information and can be helpful in forensic casework for individual identification among these populations.

Indexed as

Genetics, PopulationGenotyping TechniquesPolymorphism, Single NucleotideDNADNA FingerprintingEthnicityGene FrequencyHapMap ProjectHeterozygoteHumansRacial GroupsRetrospective StudiesDNAArrayForensic geneticsIndividual identificationRandom match probabilitySingle nucleotide polymorphism

Identifiers

PMID26297200
OpenAlexW1159436012

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Registered trials

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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.