Sep 2026· Frontiers in Bioinformatics· 0 citations· 33 references
TL;DR
DeepCelllify is introduced, a novel deep learning-based framework that harnesses convolutional neural networks (CNNs) to classify patients using their individual cell expression profiles, and demonstrates competitive performance compared to state-of-the-art approaches.
Abstract
Single-cell RNA sequencing (scRNA-seq) enables gene expression profiling at the resolution of individual cells, revealing cellular heterogeneity that is obscured in bulk RNA-seq. While this offers a powerful lens to study disease-specific changes, leveraging scRNA-seq data for patient phenotype classification remains challenging due to limited sample numbers, cell count variability, high dimensionality, and dependence on cell-type annotations. Existing tools attempt to address these issues using probabilistic models or attention mechanisms, but face limitations in scalability, interpretability, or representational power.
In this work, we introduce DeepCelllify, a novel deep learning-based framework that harnesses convolutional neural networks (CNNs) to classify patients using their individual cell expression profiles. Our approach converts tabular gene expression data into image-like representations, enabling CNNs to learn spatial feature relationships between genes. Each cell is treated as an independent input labeled by its originating patient’s condition (e.g., disease or control), allowing us to sidestep the limitations posed by small patient cohorts and heterogeneous cell counts. The DeepCelllify pipeline includes a transformation module for data preprocessing and a classification module, culminating in CNN models trained through cross-validation to differentiate between disease states based on single-cell inputs.
Our method demonstrates competitive performance compared to state-of-the-art approaches, with added benefits in scalability, interpretability, and practical applicability. DeepCelllify further addresses critical bottlenecks in scRNA-seq-based phenotype prediction, including overfitting from low patient counts, challenges in feature matrix construction, and dimensionality issues. Additionally, our method provides interpretability by assigning weights to individual cells, helping to down-weight misclassified or noisy cells.
This work introduces deep learning framework for patient phenotype prediction from scRNA-seq data, with potential applications in precision medicine and biomarker discovery.
This work introduces a two-stage statistical framework for interpretable patient-level disease classification from single-cell data, and recovered biologically coherent, cell-type specific gene signatures consistent with known disease mechanisms, demonstrating improved interpretability without sacrificing predictive ac...
Zhi-Wei Xiao, William Torous, Jeffrey B. Cheng et al.· bioRxiv· 0 citations
Single-cell transcriptomics has been revolutionising the discovery of human cell types and disease mechanisms. Accurate human cell-subtype annotation in complex neural tissues and disorders remains challenging due to the scarcity of postmortem tissue availability, in vitro culture-specific influences in surrogate m...
Muhammad Umar, András Lakatos, Arif Mahmood et al.· Scientific Reports· 0 citations
Automated cell-type annotation is a prerequisite for nearly all single-cell RNA-sequencing (scRNA-seq) analysis, and the proliferation of annotation tools — spanning marker-based, similarity-based, classical machine-learning, deep-learning, semi-supervised, large language model (LLM), and transformer foundation-model f...
AI and deep learning have transformed single-cell transcriptomics, empowering unsupervised annotation, trajectory inference, and cross-dataset integration at scale. Here, we propose bulk RNA-seq deconvolution as a novel task for single-cell foundation models. Deconvolution estimates cell type proportions from bulk RNA-...
Ali Oku, Heather Geiger, N. Robine et al.· bioRxiv· 0 citations
How scRNA-seq can be used to identify important areas of glioblastoma treatment resistance, evaluate current glioblastoma scRNA-seq-based deep learning models, and outline relevant training datasets to overcome patient scRNA-seq data availability limitations are explained.
Marybeth G. Yonk, Mainak Mustafi, Megan A Lim et al.· Frontiers in Genetics· 0 citations
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