ArticleBioinformatics (Oxford, England)2025
Incorporating hierarchical information into multiple instance learning for patient phenotype prediction with single-cell RNA-sequencing data.
Article in Bioinformatics (Oxford, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed.
- Cell-level random splits leak group-owned answers in single-cell benchmarks.bioRxiv : the preprint server for biology · 2026Article
- Annotation-free phenotype prediction using knowledge-augmented clustering from single-cell RNA sequencing data.Briefings in bioinformatics · 2026Article
- scVIP: personalized modeling of single-cell transcriptomes for developmental and disease phenotypes.bioRxiv : the preprint server for biology · 2026Article
- DREAMER-S: Deep leaRning-Enabled Attention-based Multiple-instance approaches with Explainable Representations for Spatial biology.PLoS computational biology · 2026Article
- scMILD: Single-cell multiple instance learning for sample classification and associated subpopulation discovery.iScience · 2026Article
- Exploring phenotype-related single-cells through attention-enhanced representation learning.Genome medicine · 2026Article
- ClinIAN: Clinically Informed Attention Network.Bioinformatics advances · 2026Article
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2 authors.
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Abstract
motivationMultiple instance learning (MIL) provides a structured approach to patient phenotype prediction with single-cell RNA-sequencing (scRNA-seq) data. However, existing MIL methods tend to overlook the hierarchical structure inherent in scRNA-seq data, especially the biological groupings of cells or cell types. This limitation may lead to suboptimal performance and poor interpretability at higher levels of cellular division.
resultsTo address this gap, we present a novel approach to incorporate hierarchical information into the attention-based MIL framework. Specifically, our model applies the attention-based aggregation mechanism over both cells and cell types, thus enforcing a hierarchical structure on the flow of information throughout the model. Across extensive experiments, our proposed approach demonstrates highly competitive performance and shows robustness against limited sample sizes. Moreover, ablation test results show that simply applying the attention mechanism on cell types instead of cells leads to improved performance, underscoring the benefits of incorporating the hierarchical groupings. By identifying the critical cell types that are most relevant for prediction, we show that our model is capable of capturing biologically meaningful associations, suggesting its potential to facilitate biological discoveries. AVAILABILITY AND IMPLEMENTATION: Our source code is available at https://github.com/minhchaudo/hier-mil. All datasets used in this study are publicly available online.
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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.