Evidence map›Paper›PMID 29177704›Full record

ArticleInternational journal of legal medicine2018

Inconsistent genotyping call at DYS389 locus and implications for interpretation.

Zhiyong Liu, Dongtao Jia, Jingjing Zhang, Chen Li, Xi Zhang, Yaran Yang, Meng Yang, Man Chen, Zailiang Yu, Yan Wang and 1 more

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 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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.

  1. Article
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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.

Zhiyong LiuCAS Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, NO.1 Beichen West Road, Chaoyang District, 100101, Beijing, People's Republic of China.
Dongtao JiaNantong Bureau of Public Safety, 226000, Nantong, Jiangsu, People's Republic of China.
Jingjing ZhangBeijing 3i Forensics Technology Co., Ltd, 100192, Beijing, People's Republic of China.
Chen LiBeijing Microread Genetics Co., Ltd, 100089, Beijing, People's Republic of China.
Xi ZhangBeijing 3i Forensics Technology Co., Ltd, 100192, Beijing, People's Republic of China.
Yaran YangCAS Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, NO.1 Beichen West Road, Chaoyang District, 100101, Beijing, People's Republic of China.
Meng YangCAS Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, NO.1 Beichen West Road, Chaoyang District, 100101, Beijing, People's Republic of China.
Man ChenCAS Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, NO.1 Beichen West Road, Chaoyang District, 100101, Beijing, People's Republic of China.
Zailiang YuBeijing Microread Genetics Co., Ltd, 100089, Beijing, People's Republic of China.
Yan WangBeijing 3i Forensics Technology Co., Ltd, 100192, Beijing, People's Republic of China.
Jiangwei YanCAS Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, NO.1 Beichen West Road, Chaoyang District, 100101, Beijing, People's Republic of China. yanjw@big.ac.cn.

Funding

National Natural Science Foundation of China 81330073
6 · The paper itself

Abstract

The male-specific Y chromosome short tandem repeat (STR) locus is used widely in forensic case, which are useful molecular tool to providing the biological evidence for male/female mixture and paternal lineage cases. The Y-STR analysis has been greatly facilitated by advent of commercial multiplex kit. However, even with well-designed robust multiplex kit, abnormal genotyping profile may be observed when encountering with mutations, such as deletion/duplication within the target region or mutation at the primer binding site. In this study, a single-allele shift by five nucleotides for the DYS389I marker between the AmpFlSTR

Indexed as

Chromosomes, Human, YDNA FingerprintingGenetic MarkersGenotypeMutationAsian PeopleChinaFemaleHigh-Throughput Nucleotide SequencingHumansMaleMicrosatellite RepeatsPolymerase Chain ReactionPolymorphism, Single NucleotideSequence Analysis, DNAGenetic MarkersDYS389GenotypingMutationSequencingY-STR

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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.