Evidence map›Paper›PMID 41749075›Full record

ArticleBMC bioinformatics2026

Semisupervised approach for dominant gene selection and classification.

Reshma Rastogi, Mamta Bhattarai Lamsal

Abstract read
In one paragraph

Article in BMC bioinformatics, 2026. 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.

Reshma RastogiMLSI Lab, Dept. of Computer Science and Engineering, South Asian University, Rajpur Road, Maidan Garhi, 110068, New Delhi, India.ORCID http://orcid.org/0000-0002-9322-4251
Mamta Bhattarai LamsalMLSI Lab, Dept. of Computer Science and Engineering, South Asian University, Rajpur Road, Maidan Garhi, 110068, New Delhi, India. mamta@students.sau.ac.in.ORCID http://orcid.org/0009-0000-1490-8034

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSemisupervised learning has attracted significant interest in gene expression analysis due to its ability to improve classification performance under limited labeled data, a common challenge arising from high dimensionality and small sample sizes. Existing semisupervised methods often rely on manifold learning to propagate label information; however, weak label connections in early learning stages can reduce their effectiveness.

resultsTo address these limitations, we propose a semisupervised approach for dominant gene selection and classification (SADGSC) that employs feature decomposition to identify essential features while suppressing noise and redundancy. The proposed method adopts hinge loss instead of square loss for label prediction and constructs a projection matrix based on confidence-weighted features, leading to improved classification accuracy and interpretability. Biological analysis of the top-ranked genes (e.g., PGR, KRT14, TOX3, and FGF10) reveals enrichment in hormone signaling epithelial-mesenchymal transition, apoptosis, and oxidative stress pathways, demonstrating the biological relevance of the selected genes. Experimental evaluations conducted on eleven datasets, primarily gene expression datasets, show that SADGSC achieves competitive performance compared with state-of-the-art methods.

conclusionsThe proposed SADGSC framework effectively addresses the challenges of limited labeled data and high dimensionality in gene expression analysis, providing strong classification performance and biologically meaningful gene selection. These findings highlight the potential of semisupervised learning for dominant gene discovery and robust classification in high-dimensional biological datasets.

Indexed as

Computational BiologyGene Expression ProfilingGenes, DominantSupervised Machine LearningAlgorithmsClassification AlgorithmsHumansDominant featuresFeature decompositionGene selectionNoisy featuresSemisupervised learning

Identifiers

PMID41749075
PMCPMC13041400

What Socratic 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 Socratic graph.