Evidence map›Paper›PMID 30982129›Full record

ArticleInternational journal of legal medicine2019

Novel Y-chromosome short tandem repeat sequence variation for loci DYS710, DYS518, DYS385, DYS644, DYS612, DYS626, DYS504, DYS481, DYS447 and DYS449.

Mohaimin Kasu, Jamie Fredericks, Mischa Fraser, Christiaan Labuschagne, Mpasi Lesaoana, Maria Eugenia D'Amato

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Article in International journal of legal medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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4citing papers in PubMed
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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

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3 · Its place in the literature

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4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Mohaimin KasuForensic DNA Laboratory, Department of Biotechnology, University of the Western Cape, Bellville, 7535, South Africa.
Jamie FredericksForensic DNA Laboratory, Department of Biotechnology, University of the Western Cape, Bellville, 7535, South Africa.
Mischa FraserInqaba Biotechnical Industries, Muckleneuk, Pretoria, 0002, South Africa.
Christiaan LabuschagneInqaba Biotechnical Industries, Muckleneuk, Pretoria, 0002, South Africa.
Mpasi LesaoanaForensic DNA Laboratory, Department of Biotechnology, University of the Western Cape, Bellville, 7535, South Africa.
Maria Eugenia D'AmatoForensic DNA Laboratory, Department of Biotechnology, University of the Western Cape, Bellville, 7535, South Africa. medamato@uwc.ac.za.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In forensic casework, Y-chromosome short tandem repeats (Y-STRs) are essential for differentiating between unrelated males and resolving the male component of admixed biological evidence. While the majority of Y-STRs are adequate for discriminating between different paternal lineages, rapidly mutating Y-STRs are necessary for improving discrimination between males within populations of low Y-chromosome diversity and between paternal relatives. Alternatively, sequencing of Y-STRs may also improve the discrimination between isometric Y-STR alleles by identifying variation in the repeat unit pattern arrangements and by identifying SNPs in the flanking region or within the STR repeat unit itself. In this report, a total of 153 DNA sequences are presented across the Y-STR loci DYS710, DYS518, DYS385, DYS644, DYS612, DYS626, DYS504, DYS481, DYS447 and DYS449. A total of 94 Y-STR sequences provided herein are reported for the first time, of which 37 sequences represent alleles showing size homoplasy, 34 sequences of known alleles for which sequence data has been unavailable and a total of 23 novel allele sequences across loci DYS644, DS447, DYS710 and DYS504. This study further encountered a rare sequence variant in the 5' flanking region of DYS385 and a total of two SNPs in the repeat structure at DYS481 and DYS449.

Indexed as

Chromosomes, Human, YGenetic VariationMicrosatellite RepeatsSequence Analysis, DNA5' Flanking RegionAllelesDNA FingerprintingGenetic MarkersHumansMalePolymerase Chain ReactionGenetic MarkersForensicRapidly mutatingSequence variationSize homoplasyY-chromosome; haplotype

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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.