Evidence map›Paper›PMID 42157103›Full record

ArticleBMC genomics2026

lcUMAPtSNE: use of non-linear dimensionality reduction techniques with genotype likelihoods.

Kerem Uzel, Christine Grossen, F Gözde Çilingir

Abstract read
In one paragraph

Article in BMC genomics, 2026. 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. Article
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

3 authors.

Kerem UzelBrain Research Institute, Laboratory of Neuroepigenetics, University of Zurich, Zurich, Switzerland.
Christine GrossenSwiss Federal Research Institute WSL, Biodiversity and Conservation Biology Research Unit, Birmensdorf, Switzerland.
F Gözde ÇilingirSwiss Federal Research Institute WSL, Biodiversity and Conservation Biology Research Unit, Birmensdorf, Switzerland. fgcilingir@gmail.com.

Funding

UZH Postdoc Grant FK-22-109
6 · The paper itself

Abstract

backgroundUnderstanding population structure is essential for conservation genetics, as it provides insights into population connectivity and supports the development of targeted strategies to preserve genetic diversity and adaptability. T-distributed stochastic neighbor embedding (t-SNE) and uniform manifold approximation and projection (UMAP) have proven effective for revealing population genetic structures in human and model organisms using hard-called genotypes, but their application in wild species using genotype likelihoods from low coverage sequencing (as a cost-saving measure) remains underexplored.

resultsHere, we present a Jupyter Notebook-based workflow that facilitates the use of UMAP and t-SNE on genotype likelihood-derived principal components. This workflow is demonstrated using medium to low-coverage whole-genome sequencing data from scimitar-horned oryx, which has been reintroduced into the wild and faces multiple conservation challenges.

conclusionDetailed guidance on hyperparameter tuning and practical implementation is also provided, enhancing the application of these methods in wildlife genetics to potentially support biodiversity conservation. lcUMAPtSNE is designed as a complementary and exploratory dimensionality reduction tool, rather than a replacement or benchmarking framework, and its strengths are demonstrated here using empirical data.

Indexed as

GenomicsGenotypeSoftwareAlgorithmsAnimalsDimensionality ReductionGenetics, PopulationLikelihood FunctionsConservation genomicsGenotype likelihoodsLow-coverage sequencingNon-linear dimensionality reductiont-SNEUMAP

Identifiers

PMID42157103
PMCPMC13353002

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.