Evidence map›Paper›PMID 38950178›Full record

ArticleBioinformatics (Oxford, England)2024

DeepGSEA: explainable deep gene set enrichment analysis for single-cell transcriptomic data.

Guangzhi Xiong, Nathan J LeRoy, Stefan Bekiranov, Nathan C Sheffield, Aidong Zhang

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Article in Bioinformatics (Oxford, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

5 authors.

Guangzhi XiongDepartment of Computer Science, University of Virginia, Charlottesville, VA, 22904, United States.ORCID 0000-0002-8049-5298
Nathan J LeRoyCenter for Public Health Genomics, University of Virginia, Charlottesville, VA, 22904, United States.ORCID 0000-0002-7354-7213
Stefan BekiranovDepartment of Biochemistry and Molecular Genetics, University of Virginia, Charlottesville, VA, 22908, United States.
Nathan C SheffieldCenter for Public Health Genomics, University of Virginia, Charlottesville, VA, 22904, United States.ORCID 0000-0001-5643-4068
Aidong ZhangDepartment of Computer Science, University of Virginia, Charlottesville, VA, 22904, United States.ORCID 0000-0001-9723-3246

Funding

Novel methods for large-scale genomic interval comparisonR01HG012558 · NHGRI · UNIVERSITY OF VIRGINIA · PI SHEFFIELD, NATHAN · 2022 to 2025
$1.8M
Continually Adaptive Machine Learning Platform for Personalized Biomedical Literature Curation and ExplorationR01LM014012 · NLM · UNIVERSITY OF VIRGINIA · PI TIMOTHY W CLARK, Nathan Sheffield · 2023 to 2026
$1.3M
National Science Foundation 2313865NHGRI NIH HHS R01 HG012558NIH HHS 1R01LM014012
6 · The paper itself

Abstract

motivationGene set enrichment (GSE) analysis allows for an interpretation of gene expression through pre-defined gene set databases and is a critical step in understanding different phenotypes. With the rapid development of single-cell RNA sequencing (scRNA-seq) technology, GSE analysis can be performed on fine-grained gene expression data to gain a nuanced understanding of phenotypes of interest. However, with the cellular heterogeneity in single-cell gene profiles, current statistical GSE analysis methods sometimes fail to identify enriched gene sets. Meanwhile, deep learning has gained traction in applications like clustering and trajectory inference in single-cell studies due to its prowess in capturing complex data patterns. However, its use in GSE analysis remains limited, due to interpretability challenges.

resultsIn this paper, we present DeepGSEA, an explainable deep gene set enrichment analysis approach which leverages the expressiveness of interpretable, prototype-based neural networks to provide an in-depth analysis of GSE. DeepGSEA learns the ability to capture GSE information through our designed classification tasks, and significance tests can be performed on each gene set, enabling the identification of enriched sets. The underlying distribution of a gene set learned by DeepGSEA can be explicitly visualized using the encoded cell and cellular prototype embeddings. We demonstrate the performance of DeepGSEA over commonly used GSE analysis methods by examining their sensitivity and specificity with four simulation studies. In addition, we test our model on three real scRNA-seq datasets and illustrate the interpretability of DeepGSEA by showing how its results can be explained. AVAILABILITY AND IMPLEMENTATION: https://github.com/Teddy-XiongGZ/DeepGSEA.

Indexed as

Deep LearningSingle-Cell AnalysisTranscriptomeComputational BiologyGene Expression ProfilingHumansNeural Networks, ComputerSequence Analysis, RNASoftware

Identifiers

PMID38950178
PMCPMC11236288

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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.