Evidence map›Paper›PMID 40341774›Full record

ArticleEuropean journal of human genetics : EJHG2025

UYSD: a novel data repository accessible via public website for worldwide population frequencies of Y-SNP haplogroups.

Arwin Ralf, Dion Zandstra, Bram van Wersch, Zehra Köksal, Maarten H D Larmuseau, Alexandra Rosa, Mark A Jobling, Maria E D'Amato, Cornelius Courts, Mario Gysi and 45 more

Abstract read
In one paragraph

Article in European journal of human genetics : EJHG, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Forensic genetics in the omics era.Nature reviews. Genetics · 2026
    Review
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

55 authors.

Arwin RalfDepartment of Genetic Identification, Erasmus MC University Medical Center Rotterdam, Rotterdam, the Netherlands. a.ralf@erasmusmc.nl.ORCID 0000-0001-6052-0807
Dion ZandstraDepartment of Genetic Identification, Erasmus MC University Medical Center Rotterdam, Rotterdam, the Netherlands.ORCID 0000-0002-2197-6315
Bram van WerschDepartment of Genetic Identification, Erasmus MC University Medical Center Rotterdam, Rotterdam, the Netherlands.
Zehra KöksalDepartment of Genetic Identification, Erasmus MC University Medical Center Rotterdam, Rotterdam, the Netherlands.ORCID 0000-0002-0914-9384
Maarten H D LarmuseauLaboratory of Human Genetic Genealogy, Department Human Genetics, KU Leuven, Leuven, Belgium.ORCID 0000-0002-5974-7235
Alexandra RosaUniversity of Madeira, Funchal, Portugal.
Mark A JoblingUniversity of Leicester, Leicester, United Kingdom.
Maria E D'AmatoUniversity of the Western Cape, Western Cape, South Africa.
Cornelius CourtsUniversity Hospital of Cologne, Institute of Legal Medicine, Cologne, Germany.ORCID 0000-0002-9811-8482
Mario GysiUniversity of Zurich, Zurich, Switzerland.
Cordula HaasUniversity of Zurich, Zurich, Switzerland.ORCID 0000-0001-8122-1427
Rodrigo FloresUniversity of Tartu, Tartu, Estonia.
Maximilian NeisUniversity Hospital of Cologne, Institute of Legal Medicine, Cologne, Germany.ORCID 0000-0002-8817-8668
Jon H WettonUniversity of Leicester, Leicester, United Kingdom.ORCID 0000-0001-8337-4654
Kevin KieslerNational Institute of Standards and Technology, Gaithersburg, MD, USA.
Adam AmeurDepartment of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.ORCID 0000-0001-6085-6749
Simon AzonbakinUniversity of Madeira, Funchal, Portugal.
Alexandra BôžikováInstitute of Forensic Science, Bratislava, Slovak Republic.
Andrej ChomaInstitute of Forensic Science, Bratislava, Slovak Republic.
Maria Corazon De UngriaUniversity of the Philippines Diliman, Quezon City, Philippines.
Beatrice CorradiniInstitute of Legal Medicine, University of Modena and Reggio Emilia, Modena, Italy.
Catarina CruzUniversity of Madeira, Funchal, Portugal.
Bettina DunkelmannUniversity of Salzburg, Salzburg, Austria.
Gianmarco FerriInstitute of Legal Medicine, University of Modena and Reggio Emilia, Modena, Italy.
Jan FleckhausLudwig Maximilian University, Institute of Legal Medicine, Munich, Germany.
Domniki FragouAristotle University of Thessaloniki, Thessaloniki, Greece.
Noah GaensLaboratory of Human Genetic Genealogy, Department Human Genetics, KU Leuven, Leuven, Belgium.ORCID 0009-0006-4871-2287
Rita GonçalvesUniversity of Madeira, Funchal, Portugal.
Dubravka Havaš AuguštinInstitute for Anthropological Research, Zagreb, Croatia.
Katharina HelmUniversity of Salzburg, Salzburg, Austria.
Petra Hölzl-MüllerInstitute of Legal Medicine, Medical University of Innsbruck, Innsbruck, Austria.
Michał KaliszanMedical University of Gdansk, Gdańsk, Poland.
Mohaimin KasuUniversity of the Western Cape, Western Cape, South Africa.
Leda KovatsiAristotle University of Thessaloniki, Thessaloniki, Greece.
Mpasi LesaoanaUniversity of the Western Cape, Western Cape, South Africa.
Natsuko MizunoNational Research Institute of Police Science, Kashiwa, Japan.
Franz NeuhuberUniversity of Salzburg, Salzburg, Austria.
Jana NováčkováInstitute of Criminalistics, Prague, Czech Republic.
Alena ŇuňukováInstitute of Forensic Science, Bratislava, Slovak Republic.
Horolma PamjavHungarian Institute for Forensic Sciences, Institute of Forensic Genetics, Budapest, Hungary.
Walther ParsonInstitute of Legal Medicine, Medical University of Innsbruck, Innsbruck, Austria.ORCID 0000-0002-5692-2392
Yerlan RamankulovNazarbayev University, Astana, Kazakhstan.
Héctor Rangel VillalobosUniversity of Guadalajara, Guadalajara, Mexico.
Krzysztof RębałaMedical University of Gdansk, Gdańsk, Poland.
Siiri RootsiUniversity of Tartu, Tartu, Estonia.
Jazelyn SalvadorUniversity of the Philippines Diliman, Quezon City, Philippines.ORCID 0000-0003-0223-4532
Jelena ŠaracInstitute for Anthropological Research, Zagreb, Croatia.
Carolyn R SteffenNational Institute of Standards and Technology, Gaithersburg, MD, USA.
Vlastimil StenzlInstitute of Criminalistics, Prague, Czech Republic.
Tibor TörökUniversity of Szeged, Szeged, Hungary.
Richard VillemsUniversity of Tartu, Tartu, Estonia.
Haruhiko WatahikiNational Research Institute of Police Science, Kashiwa, Japan.
Maxat ZhabaginNazarbayev University, Astana, Kazakhstan.ORCID 0000-0003-3414-0610
Peter M SchneiderUniversity Hospital of Cologne, Institute of Legal Medicine, Cologne, Germany.
Manfred KayserDepartment of Genetic Identification, Erasmus MC University Medical Center Rotterdam, Rotterdam, the Netherlands. m.kayser@erasmusmc.nl.ORCID 0000-0002-4958-847X

Funding

EC | Horizon 2020 Framework Programme (EU Framework Programme for Research and Innovation H2020) 101080117Eesti Teadusagentuur (Estonian Research Council) PRG1071
6 · The paper itself

Abstract

For decades, there has been scientific interest in the variation and geographic distribution of paternal lineages associated with the human Y chromosome. However, the relevant data have been dispersed across numerous publications, making it difficult to consolidate. Additionally, understanding the relationships between different variants, and the tools used to analyze them, have evolved over time, further complicating efforts to harmonize this information. The Universal Y-SNP Database (UYSD) marks a substantial advancement by providing a comprehensive and accessible platform for Y-SNP and haplogroup data from populations around the world. UYSD harmonizes diverse datasets into a unified repository, facilitating the exploration of global Y-chromosomal variation. The platform handles data generated with both high- and low-throughput technology and is compatible with the automated analysis software tool, Yleaf v3. Key functionalities include the ability to: i) visualize haplogroup distributions on an interactive world map, ii) estimate haplogroup frequencies in geographic regions with sparse data through interpolation, and iii) display detailed phylogenetic trees of Y-chromosomal haplogroups. Currently, UYSD encompasses data from over 6,600 males across 27 populations. This dataset largely aligns with known global Y-haplogroup patterns, but also reveals unexplored finer-scale geographic variations. While the present dataset is largely European-centered, UYSD is designed for ongoing expansion by the scientific community, aiming to include more global data and higher-resolution population sequencing data. The platform thus offers valuable insights into human genetic diversity and migration patterns, serving several fields of research such as: human population genetics, genetic anthropology, ancient DNA analysis and forensic genetics.

Indexed as

Chromosomes, Human, YDatabases, GeneticHaplotypesPolymorphism, Single NucleotideGenetics, PopulationHumansMalePhylogenySoftware

Identifiers

PMID40341774
PMCPMC12229683

What OpenQuestion holds

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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.