Evidence map›Paper›PMID 28887705›Full record

ArticleInternational journal of legal medicine2018

Population data and mutation rates of 20 autosomal STR loci in a Chinese Han population from Yunnan Province, Southwest China.

Xiufeng Zhang, Linlin Liu, Runfang Xie, Guiyi Wang, Yuan Shi, Tao Gu, Liping Hu, Shengjie Nie

Abstract read
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In one paragraph

Article in International journal of legal medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.5field-weighted citation impact, top 15% 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

5 citing papers in PubMed, 15 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

8 authors at 2 institutions in 1 country.

Xiufeng ZhangSchool of Forensic Medicine, Kunming Medical University, Kunming, Yunnan Province, People's Republic of China.
Linlin LiuSchool of Forensic Medicine, Kunming Medical University, Kunming, Yunnan Province, People's Republic of China.
Runfang XieSchool of Forensic Medicine, Kunming Medical University, Kunming, Yunnan Province, People's Republic of China.
Guiyi WangSchool of Forensic Medicine, Kunming Medical University, Kunming, Yunnan Province, People's Republic of China.
Yuan ShiSchool of Forensic Medicine, Kunming Medical University, Kunming, Yunnan Province, People's Republic of China.
Tao GuCenter for Disease Prevention and Control of Kunming, Kunming, Yunnan Province, People's Republic of China. gutaokm@qq.com.
Liping HuSchool of Forensic Medicine, Kunming Medical University, Kunming, Yunnan Province, People's Republic of China. ping772150@163.com.
Shengjie NieSchool of Forensic Medicine, Kunming Medical University, Kunming, Yunnan Province, People's Republic of China. nieshengjie@126.com.
Kunming Medical University · CNYunnan Center for Disease Control And Prevention · CN

Funding

the Natural Science Foundation of China 31660310the Science and Technology Planning Projects of Yunnan Province 2013FZ066the Science and Technology Planning Projects of Yunnan Province 2014FZ005the Yunnan Educational Science Foundation program 2014Y180
6 · The paper itself

Abstract

The genetic polymorphisms of 20 autosomal short tandem repeat (STR) loci included in the PowerPlex® 21 kit were evaluated from 2068 unrelated, healthy individuals from the Chinese Han population of Yunnan Province in southwest China. All of the loci reached Hardy-Weinberg equilibrium. These loci were examined to determine allele frequencies and forensic statistical parameters. The genetic relationships among the Yunnan Han and other Chinese populations were also estimated. The combined discrimination power and probability of excluding paternity of the 20 STR loci were 0.99999999999999999999999126 and 0.999999975, respectively. In addition, mutation rates from 4363 parentage cases (2215 trios and 2148 duos) were investigated in this study. A total of 164 mutations were observed in 6578 meioses from the 20 loci. The highest mutation rate was observed in D12S391 (0.30%), and the lowest mutation rates were observed in D13S317 (0.03%) and TPOX (0.03%). The average mutation rate for the 20 loci was estimated to be 1.246 × 10

Indexed as

Genetics, PopulationMicrosatellite RepeatsMutation RateAsian PeopleChinaDNA FingerprintingEthnicityFemaleGene FrequencyHumansMalePolymerase Chain ReactionChinese HanMutation ratePopulation dataShort tandem repeat (STR)Yunnan Province

Identifiers

PMID28887705
OpenAlexW2755326203

What OpenQuestion holds

Textmetadata
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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.