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TSCytoPred: a deep learning framework for inferring cytokine expression trajectories from irregular longitudinal gene
Joung Min Choi1, Heejoon Chae2
1Department of Computer Science, Virginia Polytechnic Institute and State University (Virginia Tech), Blacksburg, VA, United States of America.
This study introduces TSCytoPred, a deep learning model that infers cytokine expression trajectories from gene expression data. This method enhances disease severity prediction and aids in analyzing longitudinal data for improved patient outcomes.
Area of Science:
- Immunology and Computational Biology
- Biomarker Discovery and Predictive Modeling
Background:
- Cytokines are critical immune regulators, but their dysregulation is linked to severe diseases like cancer and COVID-19.
- Longitudinal cytokine profiling is essential for predicting disease severity and patient outcomes, yet data is often limited.
- Computational inference of cytokine expression from gene expression data offers a promising approach to overcome data scarcity.
Purpose of the Study:
- To develop and validate TSCytoPred, a deep learning model for inferring time-series cytokine expression trajectories from gene expression data.
- To assess the model's performance in predicting cytokine dynamics and its utility in clinical disease prediction.
- To address limitations in current time-series cytokine data availability for robust predictive modeling.
Main Methods:
- TSCytoPred utilizes deep learning on time-series gene expression data, identifying key genes through interaction relationships and correlations.
- A neural network with an interpolation block estimates cytokine expression trajectories between observed time points.
- The model was evaluated using a COVID-19 dataset, comparing its performance against baseline regression methods.
Main Results:
- TSCytoPred significantly outperformed baseline methods, achieving high R² and low MAE in cytokine expression trajectory inference.
- Inferred cytokine data from TSCytoPred improved the prediction of COVID-19 patient severity risk.
- The model demonstrated effectiveness on datasets with limited time points and irregular temporal gaps.
Conclusions:
- TSCytoPred provides a robust method for inferring cytokine expression dynamics, addressing limitations of sparse time-series data.
- The model enhances the clinical utility of multi-omics data for disease outcome analysis, particularly in contexts like COVID-19.
- TSCytoPred facilitates early disease detection, treatment response prediction, and expands the application of multi-omics in rare diseases.
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