Evidence map›Paper›PMID 39820437›Full record

ArticleBriefings in bioinformatics2024

scGO: interpretable deep neural network for cell status annotation and disease diagnosis.

You Wu, Pengfei Xu, Liyuan Wang, Shuai Liu, Yingnan Hou, Hui Lu, Peng Hu, Xiaofei Li, Xiang Yu

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Pathway-guided architectures for interpretable AI in biological research.Computational and structural biotechnology journal · 2025
    Review
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

9 authors.

You WuSchool of Life Sciences and Biotechnology, Shanghai Jiao Tong University, No. 800 Dong Chuan Road, Shanghai 200240, China.
Pengfei XuSchool of Life Sciences and Biotechnology, Shanghai Jiao Tong University, No. 800 Dong Chuan Road, Shanghai 200240, China.
Liyuan WangSchool of Agriculture and Biology, Shanghai Jiao Tong University, No. 800 Dong Chuan Road, Shanghai 200240, China.
Shuai LiuSchool of Life Sciences and Biotechnology, Shanghai Jiao Tong University, No. 800 Dong Chuan Road, Shanghai 200240, China.
Yingnan HouSchool of Agriculture and Biology, Shanghai Jiao Tong University, No. 800 Dong Chuan Road, Shanghai 200240, China.
Hui LuSchool of Life Sciences and Biotechnology, Shanghai Jiao Tong University, No. 800 Dong Chuan Road, Shanghai 200240, China.
Peng HuMinistry of Education, Shanghai Ocean University, No. 999, Huchenghuan Road, Shanghai 201306, China.
Xiaofei LiSchool of Life Sciences and Biotechnology, Shanghai Jiao Tong University, No. 800 Dong Chuan Road, Shanghai 200240, China.
Xiang YuSchool of Life Sciences and Biotechnology, Shanghai Jiao Tong University, No. 800 Dong Chuan Road, Shanghai 200240, China.ORCID 0000-0002-5730-8802

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Machine learning has emerged as a transformative tool for elucidating cellular heterogeneity in single-cell RNA sequencing. However, a significant challenge lies in the "black box" nature of deep learning models, which obscures the decision-making process and limits interpretability in cell status annotation. In this study, we introduced scGO, a Gene Ontology (GO)-inspired deep learning framework designed to provide interpretable cell status annotation for scRNA-seq data. scGO employs sparse neural networks to leverage the intrinsic biological relationships among genes, transcription factors, and GO terms, significantly augmenting interpretability and reducing computational cost. scGO outperforms state-of-the-art methods in the precise characterization of cell subtypes across diverse datasets. Our extensive experimentation across a spectrum of scRNA-seq datasets underscored the remarkable efficacy of scGO in disease diagnosis, prediction of developmental stages, and evaluation of disease severity and cellular senescence status. Furthermore, we incorporated in silico individual gene manipulations into the scGO model, introducing an additional layer for discovering therapeutic targets. Our results provide an interpretable model for accurately annotating cell status, capturing latent biological knowledge, and informing clinical practice.

Indexed as

Computational BiologyDeep LearningGene OntologyNeural Networks, ComputerSingle-Cell AnalysisHumansMolecular Sequence Annotationcell status annotationdisease diagnosisinterpretable modelscRNA-seqsparse neural networks

Identifiers

PMID39820437
PMCPMC11737892

What Socratic 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 Socratic graph.