Evidence map›Paper›PMID 41244204›Full record

ArticlePeerJ2025

TSCytoPred: a deep learning framework for inferring cytokine expression trajectories from irregular longitudinal gene expression data to enhance multi-omics analyses.

Joung Min Choi, Heejoon Chae

Abstract read
In one paragraph

Article in PeerJ, 2025. 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

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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

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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. Longitudinal omics data analysis: approaches and applications.Computational and structural biotechnology journal · 2026
    Review
4 · The record

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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.

Joung Min ChoiDepartment of Computer Science, Virginia Polytechnic Institute and State University (Virginia Tech), Blacksburg, VA, United States of America.
Heejoon ChaeDivision of Computer Science, Sookmyung Women's University, Seoul, Republic of South Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cytokines play a crucial role in immune system regulation, mediating responses from pathogen defense to tissue-damaging inflammation. Excessive cytokine production is implicated in severe conditions such as cancer progression, hemophagocytic lymphohistiocytosis, and severe cases of Coronavirus disease-2019 (COVID-19). Studies have shown that cytokine expression profiles serve as biomarkers for disease severity and mortality prediction, with machine learning (ML) methods increasingly employed for predictive analysis. To improve patient outcome predictions, treatment adaptation, and survival rates, longitudinal analysis of cytokine profiles is essential. Time-series cytokine profiling has been linked to tumor response, overall survival in various cancers, and acute encephalopathy. Similarly, COVID-19 severity and patient outcomes correlate with cytokine expression dynamics over time. However, challenges remain due to the limited availability of time-series cytokine data, restricting broader experimental applications and robust predictive modeling. Recent advancements indicate that cytokine expression can be computationally inferred using gene expression data and transcription factor interactions. Inferring cytokine levels from existing gene expression datasets could enhance early disease detection and treatment response predictions while reducing profiling costs. This work proposes TSCytoPred, a deep learning-based model trained on time-series gene expression data to infer cytokine expression trajectories. TSCytoPred identifies genes relevant for predicting target cytokines through interaction relationships and high correlation. These identified genes are subsequently utilized in a neural network incorporating an interpolation block to estimate cytokine expression trajectories between observed time points. Performance evaluations using a COVID-19 dataset demonstrate that TSCytoPred significantly outperforms baseline regression methods, achieving the highest coefficient of determinataion (R

Indexed as

COVID-19CytokinesDeep LearningGene Expression ProfilingHumansMultiomicsSARS-CoV-2CytokinesCytokine expressionDeep learningGene expressionTime-series inference

Identifiers

PMID41244204
PMCPMC12614104

What Socratic holds

Textmetadata
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 Socratic graph.