Evidence map›Paper›PMID 40194517›Full record

ArticleGenetics2026

Dimensionality reduction of genetic data using contrastive learning.

Filip Thor, Carl Nettelblad

Abstract read
In one paragraph

Article in Genetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Advancing Normal Tissue Complication Probability Modeling with Supervised Contrastive Learning for Predicting Osteoradionecrosis.Proceedings of the ... Symposium on Applied Computing. Symposium on Applied Computing · 2026
    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

2 authors.

Filip ThorDivision of Scientific Computing, Department of Information Technology, Science for Life Laboratory, Uppsala University, Uppsala SE-752 37, Sweden.ORCID 0009-0008-5041-3256
Carl NettelbladDivision of Scientific Computing, Department of Information Technology, Science for Life Laboratory, Uppsala University, Uppsala SE-752 37, Sweden.ORCID 0000-0003-0458-6902

Funding

Formas 2020-00712Linköping University 2022-165Linköping University 2022-17Linköping University 2023-258Linköping University 2024-121National Supercomputer Centre
6 · The paper itself

Abstract

We introduce a framework for using contrastive learning for dimensionality reduction on genetic datasets to create principal component analysis (PCA)-like population visualizations. Contrastive learning is a self-supervised deep learning method that uses similarities between samples to train the neural network to discriminate between samples. Many of the advances in these types of models have been made for computer vision, but some common methodology does not translate well from image to genetic data. We define a loss function that outperforms loss functions commonly used in contrastive learning, and a data augmentation scheme tailored specifically towards SNP genotype datasets. We compare the performance of our method to PCA and contemporary nonlinear methods with respect to how well they preserve local and global structure, and how well they generalize to new data. Our method displays good preservation of global structure and has improved generalization properties over t-distributed stochastic neighbor embedding, Uniform Manifold Approximation and Projection, and popvae, while preserving relative distances between individuals to a high extent. A strength of the deep learning framework is the possibility of projecting new samples and fine-tuning to new datasets using a pretrained model without access to the original training data, and the ability to incorporate more domain-specific information in the model. We show examples of population classification on two datasets of dog and human genotypes.

Indexed as

Deep LearningAlgorithmsAnimalsDimensionality ReductionHumansNeural Networks, ComputerPolymorphism, Single NucleotidePrincipal Component Analysisdeep learningdimensionality reductionmachine learningPCApopulation genetics

Identifiers

PMID40194517
PMCPMC12774828

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.