Evidence map›Paper›PMID 36226179›Full record

ArticleFrontiers in genetics2022

The application of short and highly polymorphic microhaplotype loci in paternity testing and sibling testing of temperature-dependent degraded samples.

Dan Wen, Hao Xing, Ying Liu, Jienan Li, Weifeng Qu, Wei He, Chudong Wang, Ruyi Xu, Yi Liu, Hongtao Jia and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
1.0field-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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 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

11 authors at 1 institution in 1 country.

Dan WenDepartment of Forensic Medicine, School of Basic Medical Sciences, Central South University, Changsha, China.
Hao XingDepartment of Forensic Medicine, School of Basic Medical Sciences, Central South University, Changsha, China.
Ying LiuXiangya Stomatological Collage, Central South University, Changsha, China.
Jienan LiDepartment of Forensic Medicine, School of Basic Medical Sciences, Central South University, Changsha, China.
Weifeng QuDepartment of Forensic Medicine, School of Basic Medical Sciences, Central South University, Changsha, China.
Wei HeDepartment of Forensic Medicine, School of Basic Medical Sciences, Central South University, Changsha, China.
Chudong WangDepartment of Forensic Medicine, School of Basic Medical Sciences, Central South University, Changsha, China.
Ruyi XuDepartment of Forensic Medicine, School of Basic Medical Sciences, Central South University, Changsha, China.
Yi LiuDepartment of Forensic Medicine, School of Basic Medical Sciences, Central South University, Changsha, China.
Hongtao JiaDepartment of Forensic Medicine, School of Basic Medical Sciences, Central South University, Changsha, China.
Lagabaiyila ZhaDepartment of Forensic Medicine, School of Basic Medical Sciences, Central South University, Changsha, China.
Central South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Paternity testing and sibling testing become more complex and difficult when samples degrade. But the commonly used genetic markers (STR and SNP) cannot completely solve this problem due to some disadvantages. The novel genetic marker microhaplotype proposed by Kidd's research group combines the advantages of STR and SNP and is expected to become a promising genetic marker for kinship testing in degraded samples. Therefore, in this study, we intended to select an appropriate number of highly polymorphic SNP-based microhaplotype loci, detect them by the next-generation sequencing technology, analyze their ability to detect degraded samples, calculate their forensic parameters based on the collected 96 unrelated individuals, and evaluate their effectiveness in paternity testing and sibling testing by simulating kinship relationship pairs, which were also compared to 15 STR loci. Finally, a short and highly polymorphic microhaplotype panel was developed, containing 36 highly polymorphic SNP-based microhaplotype loci with lengths smaller than 100 bp and

Indexed as

degraded samplesforensicmicrohaplotypepaternity testingsibling testing

Identifiers

PMID36226179
PMCPMC9549137
OpenAlexW4297226172

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.