Evidence map›Paper›PMID 32483669›Full record

ArticleInternational journal of legal medicine2021

Deletions and duplications of 42 Y chromosomal short tandem repeats in Chinese Han population.

Hailun Nan, Weiwei Wu, Honglei Hao, Wenran Ren, Dejian Lu

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Article in International journal of legal medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Repetitive DNA Sequences in the Human Y Chromosome and Male Infertility.Frontiers in cell and developmental biology · 2022
    Review
  3. Article
4 · The record

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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

5 authors.

Hailun NanFaculty of Forensic Medicine, Zhongshan Medical School of Sun Yat-Sen University, Guangdong Province Translational Forensic Medicine Engineering Technology Research Center of Sun Yat-Sen University, 74# Zhongshan 2nd Road, Guangzhou, 510080, People's Republic of China.
Weiwei WuInstitute of Forensic Science of Zhejiang Provincial Public Security Bureau, Zhejiang Key Laboratory of Forensic Science and Technology, 66# Minsheng Road, Hangzhou, 310009, People's Republic of China.
Honglei HaoInstitute of Forensic Science of Zhejiang Provincial Public Security Bureau, Zhejiang Key Laboratory of Forensic Science and Technology, 66# Minsheng Road, Hangzhou, 310009, People's Republic of China.
Wenran RenInstitute of Forensic Science of Zhejiang Provincial Public Security Bureau, Zhejiang Key Laboratory of Forensic Science and Technology, 66# Minsheng Road, Hangzhou, 310009, People's Republic of China.
Dejian LuFaculty of Forensic Medicine, Zhongshan Medical School of Sun Yat-Sen University, Guangdong Province Translational Forensic Medicine Engineering Technology Research Center of Sun Yat-Sen University, 74# Zhongshan 2nd Road, Guangzhou, 510080, People's Republic of China. lvdejian@mail.sysu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genotypes of 42 Y chromosome STR (Y-STR) loci were analyzed for a sample of 1420 unrelated males and 1160 father-son pairs from a Chinese Han population. Deletions of Y-STR loci were detected at DYS389I, DYS389II, DYS437, DYS446, DYS447, DYS448, and DYS557 loci. The most common deletion occurred at DYS448 and DYS557 with a frequency of 0.0056 and 0.0035, respectively. On the other hand, duplications of alleles were observed at DYF387S1a/b, DYS385a/b, DYS460, DYS527a/b, DYS459a/b, and DYS557 loci. The DYF387S1a/b, DYS527a/b, and DYS385a/b showed the highest duplicated frequencies of 0.0148, 0.0134, and 0.0099, respectively. The Y-STRs located on palindromes significantly exhibited more deletions or duplications than those non-palindromic loci. Also, duplications were more frequent than deletions. Hence, deletions or duplications of Y-STRs related to their positions on the Y chromosome. All the 52 deleted or duplicated events occurred in the two-generation families inherited stably. Furthermore, the deletions may show the Chinese Han population specificity, but the duplications may not have a similar phenomenon. Our results will be helpful to correct interpretation of the genetic profile of Y-STR loci in forensic casework.

Indexed as

Chromosome DeletionChromosome DuplicationChromosomes, Human, YMicrosatellite RepeatsAsian PeopleChinaDNA FingerprintingElectrophoresis, CapillaryEthnicityGenetics, PopulationHumansMalePolymerase Chain ReactionChinese Han populationDeletionDuplicationY chromosomal short tandem repeat (Y-STR)

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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.