Evidence map›Paper›PMID 34432235›Full record

ArticleGenes & genomics2021

Comparative analysis of allele variation using allele frequencies according to sample size in Korean population.

Hyun-Chul Park, Eu-Ree Ahn, Sang-Cheul Shin

Open access · hybridAbstract read
In one paragraph

Article in Genes & genomics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 29% 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

4 citing papers in PubMed, 5 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

3 authors at 1 institution in 1 country.

Hyun-Chul ParkForensic DNA Division, National Forensic Service Daegu Institute, Daegu, 39872, Republic of Korea. hcpark79@korea.kr.ORCID 0000-0003-2414-4378
Eu-Ree AhnForensic DNA Division, National Forensic Service Daegu Institute, Daegu, 39872, Republic of Korea.
Sang-Cheul ShinForensic DNA Division, National Forensic Service Daegu Institute, Daegu, 39872, Republic of Korea.
National Forensic Institute · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAllele frequency using short tandem repeats (STRs) is used to calculate likelihood ratio for database match, to interpret DNA mixture and to estimate ethnic groups in forensic genetics. In Korea, three population studies for 23 STR loci have been conducted with different sample size for forensic purposes.

objectiveWe performed comparative analysis to determine how the difference of sample size affects the allele frequency and allele variation within same ethnic population (i.e. Korean). Furthermore, this study was conducted to check how the sampling group and multiplex kit also affect allele variation such as rare alleles and population specific alleles.

methodsTo compare allele variation, we used allele frequencies of three population data published from three Korean forensic research groups. Allele frequencies were calculated using different sample sizes and multiplex kits: 526, 1000, and 2000 individuals, respectively.

resultsThe results showed the different distribution of allele frequencies in some loci. There was also a difference in the number of rare alleles observed by the sample size and sampling bias. In particular, an allele of 9.1 in the D2S441 locus was not observed in population study with 526 individuals due to multiplex kits.

conclusionBecause the allele frequencies play an important role in forensic genetics, even if the samples are derived from the same population, it is important to consider the effects of sample size, sampling bias, and selection of multiplex kits in population studies.

Indexed as

AllelesGenetics, PopulationAsian PeopleEthnicityForensic GeneticsGene FrequencyGenetic VariationHumansMicrosatellite RepeatsRepublic of KoreaSample SizeAllele frequencyComparative studyPopulation studySample sizeSampling bias

Identifiers

PMID34432235
PMCPMC8478755
OpenAlexW3195451445

What OpenQuestion holds

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LicenceCC BY
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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.