Evidence map›Paper›PMID 42832552›Full record

ArticlePLoS computational biology2026

A graph-attentive GAN for rare-cell-aware single-cell RNA-seq data generation.

Ritwik Ganguly, Sana Aafrine, Sk Md Mosaddek Hossain, Sumanta Ray

Abstract read
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Article in PLoS computational biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Ritwik GangulyComputer Science and Engineering, Aliah University, Kolkata, India.ORCID https://orcid.org/0009-0000-4626-3760
Sana AafrineComputer Science and Engineering, Aliah University, Kolkata, India.ORCID https://orcid.org/0009-0000-3520-9216
Sk Md Mosaddek HossainComputer Science and Engineering, Aliah University, Kolkata, India.ORCID https://orcid.org/0000-0003-0174-2359
Sumanta RayData Science, The West Bengal National University of Juridical Sciences, Kolkata, India.ORCID https://orcid.org/0000-0002-3371-8516

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A central challenge in downstream single-cell RNA sequencing (scRNA-seq) analysis is the high-dimensional, small-sample (HDSS) regime, often compounded by class imbalance from rare cell types. These factors hinder robust feature (gene) selection and cell clustering and limit the realism of samples generated by existing simulators. We introduce GARAGE, a Graph-Attentive RAre-cell aware single-cell data GEneration that augments the generator's input with a small, attention-weighted 'leakage' of real cells in addition to prior noise. Specifically, we build a k-nearest-neighbour cell graph and use a graph attention network (GAT) to prioritize nodes that likely represent under-sampled (rare) subpopulations; these high-attention cell embeddings are injected into the generator input to steer synthesis toward biologically plausible regions of the data manifold while respecting cell-type proportions. This attention-guided leakage accelerates training, reduces mode dropping, and yields realistic synthetic cells that preserve rare-cell structure. Across real scRNA-seq benchmarks, GARAGE improves downstream feature selection and clustering compared with state-of-the-art baselines. In summary, GARAGE directly addresses HDSS and rarity in scRNA-seq by coupling graph attention with adversarial generation to produce high-fidelity synthetic cells that enhance downstream analyses. The corresponding software is available at: https://github.com/RitwikGanguly/GARAGE.

Indexed as

RNA-SeqSequence Analysis, RNASingle-Cell AnalysisAlgorithmsAnimalsComputational BiologyGenerative Adversarial NetworksGraph Neural NetworksHumansSingle-Cell Gene Expression AnalysisSoftware

Identifiers

PMID42832552
PMCPMC13638049

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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.