Evidence map›Paper›PMID 40432791›Full record

ArticleNAR genomics and bioinformatics2025

TCRCluster: a novel approach to T-cell receptor latent featurization and clustering using contrastive learning-guided two-stage variational autoencoders.

Yat-Tsai Richie Wan, Morten Nielsen

Abstract read
In one paragraph

Article in NAR genomics and bioinformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Yat-Tsai Richie WanDepartment of Health Technology, Technical University of Denmark, Kgs Lyngby DK 28002, Denmark.ORCID https://orcid.org/0000-0003-0814-0289
Morten NielsenDepartment of Health Technology, Technical University of Denmark, Kgs Lyngby DK 28002, Denmark.ORCID https://orcid.org/0000-0001-7885-4311

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

T cells play a vital role in adaptive immunity by targeting pathogen-infected or cancerous cells, but predicting their specificity remains challenging. Encoding T-cell receptor (TCR) sequences into informative feature spaces is therefore crucial for advancing specificity prediction and downstream applications. For this, we developed a variational autoencoder (VAE)-based model trained on paired TCR α-β chain data, incorporating all six complementarity-determining regions. A semi-supervised 'two-stage VAE' framework, integrating cosine triplet loss and a classifier, was found to further refine peptide-specific latent representations, outperforming sequence-based methods in specificity prediction. Clustering analyses leveraging our VAE latent space were evaluated using

Indexed as

Receptors, Antigen, T-CellReceptors, Antigen, T-Cell, alpha-betaAlgorithmsAutoencoderCluster AnalysisComplementarity Determining RegionsHumansComplementarity Determining RegionsReceptors, Antigen, T-CellReceptors, Antigen, T-Cell, alpha-beta

Identifiers

PMID40432791
PMCPMC12107435

What OpenQuestion holds

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LicenceCC BY-NC
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.