Evidence map›Paper›PMID 34868274›Full record

ArticleFrontiers in genetics2021

Identification and Characterization of Nine Novel X-Chromosomal Short Tandem Repeats on Xp21.1, Xq21.31, and Xq23 Regions.

Qinrui Yang, Jinglei Qian, Chengchen Shao, Yining Yao, Zhihan Zhou, Hongmei Xu, Qiqun Tang, Xiaoqin Qian, Jianhui Xie

Open access · goldAbstract read
In one paragraph

Article in Frontiers in genetics, 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
0.7field-weighted citation impact, top 25% 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

4 citing papers in PubMed, 6 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

9 authors at 2 institutions in 1 country.

Qinrui YangDepartment of Forensic Medicine, School of Basic Medical Sciences, Fudan University, Shanghai, China.
Jinglei QianDepartment of Forensic Medicine, School of Basic Medical Sciences, Fudan University, Shanghai, China.
Chengchen ShaoDepartment of Forensic Medicine, School of Basic Medical Sciences, Fudan University, Shanghai, China.
Yining YaoDepartment of Forensic Medicine, School of Basic Medical Sciences, Fudan University, Shanghai, China.
Zhihan ZhouDepartment of Forensic Medicine, School of Basic Medical Sciences, Fudan University, Shanghai, China.
Hongmei XuDepartment of Forensic Medicine, School of Basic Medical Sciences, Fudan University, Shanghai, China.
Qiqun TangDepartment of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Fudan University, Shanghai, China.
Xiaoqin QianDepartment of Forensic Medicine, School of Basic Medical Sciences, Fudan University, Shanghai, China.
Jianhui XieDepartment of Forensic Medicine, School of Basic Medical Sciences, Fudan University, Shanghai, China.
Shanghai Medical College of Fudan University · CNFudan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The application of X-chromosomal short tandem repeats (X-STRs) has been recognized as a powerful tool in complex kinship testing. To support further development of X-STR analysis in forensic use, we identified nine novel X-STRs, which could be clustered into three linkage groups on Xp21.1, Xq21.31, and Xq23. A multiplex PCR system was built based on the electrophoresis. A total of 198 unrelated Shanghai Han samples along with 168 samples from 43 families was collected to investigate the genetic polymorphism and forensic parameters of the nine loci. Allele numbers ranged from 5 to 12, and amplicon sizes ranged from 146 to 477 bp. The multiplex showed high values for the combined power of discrimination (0.99997977 in males and 0.99999999 in females) and combined mean exclusion chances (0.99997918 and 0.99997821 in trios, 0.99984939 in duos, and 0.99984200 in deficiency cases). The linkage between all pairs of loci was estimated via Kosambi mapping function and linkage disequilibrium test, and further investigated through the family study. The data from 43 families strongly demonstrated an independent transmission between LGs and a tight linkage among loci within the same LG. All these results support that the newly described X-STRs and the multiplex system are highly promising for further forensic use.

Indexed as

kinship testinglinkagemultiplex PCRrecombinationX-chromosomal STRs

Identifiers

PMID34868274
PMCPMC8635773
OpenAlexW3212372712

What OpenQuestion holds

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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.