Evidence map›Paper›PMID 40662783›Full record

ArticleBioinformatics (Oxford, England)2025

Incorporating hierarchical information into multiple instance learning for patient phenotype prediction with single-cell RNA-sequencing data.

Chau Do, Harri Lähdesmäki

Abstract read
In one paragraph

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.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
4 · The record

Corrections and comments

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.

Chau DoDepartment of Computer Science, Aalto University, Espoo 11000, Finland.
Harri LähdesmäkiDepartment of Computer Science, Aalto University, Espoo 11000, Finland.

Funding

Cancer Foundation of FinlandResearch Council of Finland 359135Sigrid Jusélius Foundation
6 · The paper itself

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.

Indexed as

Machine LearningRNA-SeqSequence Analysis, RNASingle-Cell AnalysisAlgorithmsComputational BiologyHumansMultiple-Instance Learning AlgorithmsPhenotype

Identifiers

PMID40662783
PMCPMC12261414

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.