Evidence map›Paper›PMID 27059997›Full record

ArticleInternational journal of legal medicine2016

Genetic variation study of 12 X chromosomal STR in central Thailand population.

Kornkiat Vongpaisarnsin, Achara Boonlert, Kawin Rasmeepaisarn, Piyawan Dangkao

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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 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 22% 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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 11 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

4 authors at 2 institutions in 1 country.

Kornkiat VongpaisarnsinDepartment of Forensic Medicine, Faculty of Medicine, Chulalongkorn University, 1873 Rama4 road, Lumpini, Bangkok, 10330, Thailand. v_kornkiat@yahoo.com.
Achara BoonlertForensic Serology and DNA, King Chulalongkorn Memorial Hospital, 1873 Rama4 road, Lumpini, Bangkok, 10330, Thailand.
Kawin RasmeepaisarnDepartment of Forensic Medicine, Faculty of Medicine, Chulalongkorn University, 1873 Rama4 road, Lumpini, Bangkok, 10330, Thailand.
Piyawan DangkaoForensic Serology and DNA, King Chulalongkorn Memorial Hospital, 1873 Rama4 road, Lumpini, Bangkok, 10330, Thailand.
Chulalongkorn University · THKing Chulalongkorn Memorial Hospital · TH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genetic data from 12 short tandem repeats (STR) on the X chromosome are currently used in forensics studies to resolve issues related to complex kinship or when data is missing or ambiguous. In this study, we genotyped these 12 X chromosome STR in DNA collected from individuals from central Thailand (n = 391, 282 men and 109 women) and used this information to calculate allele and haplotype frequencies as well as forensic parameters for kinship calculations. Polymorphism information contents of the loci were range from 0.5283-0.9247, and powers of discrimination in females and males were 0.7666-0.9905 and 0.6085-0.9291, respectively. A diallelic pattern was observed at the locus DXS7132. Moreover, a comparison of genetic distance revealed a close relationship within Asian countries. Our results indicate that the X chromosomal short tandem repeat (X-STR) multiplex system provides highly informative genetic data and could be advantageous in forensic studies.

Indexed as

Chromosomes, Human, XGenetics, PopulationMicrosatellite RepeatsPolymorphism, GeneticAsian PeopleDNA FingerprintingFemaleGene FrequencyGenotypeHaplotypesHumansMaleThailandCentral ThailandHaplotypeLinkage disequilibriumShort tandem repeatX chromosome

Identifiers

PMID27059997
OpenAlexW2312523141

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.