Evidence map›Paper›PMID 38670157›Full record

ArticleBriefings in bioinformatics2024

Prior knowledge-guided multilevel graph neural network for tumor risk prediction and interpretation via multi-omics data integration.

Hongxi Yan, Dawei Weng, Dongguo Li, Yu Gu, Wenji Ma, Qingjie Liu

Open access · goldAbstract 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 30 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 2 pooled it
6.3field-weighted citation impact, top 3% of its field
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

30 citing papers in PubMed, 2 syntheses or guidelines pooled it, 27 citations in OpenAlex.

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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

6 authors at 3 institutions in 1 country.

Hongxi YanDepartment of Computer Science, Beihang University, XueYuan Road, 100191, BeiJing, China.
Dawei WengSchool of Biomedical Engineering, Capital Medical University, 10 You An Men WaiXi Tou Tiao, 100069, Beijing, China.
Dongguo LiSchool of Biomedical Engineering, Capital Medical University, 10 You An Men WaiXi Tou Tiao, 100069, Beijing, China.
Yu GuSchool of Biomedical Engineering, Capital Medical University, 10 You An Men WaiXi Tou Tiao, 100069, Beijing, China.
Wenji MaCenter for Single-Cell Omics, School of Public Health, Shanghai Jiao Tong University School of Medicine, 227 South Chongqing Road, 200025, Shanghai, China.
Qingjie LiuDepartment of Computer Science, Beihang University, XueYuan Road, 100191, BeiJing, China.
Capital Medical University · CNBeihang University · CNShanghai Jiao Tong University · CN

Funding

Beijing Natural Science Foundation L232103China Association for Science and Technology 2020QNRC001National Key R&D Program of China 2022YFC3502500National Natural Science Foundation of China 32100512National Natural Science Foundation of China 61806010Science and Technology Innovation 2030 - Brain Science and Brain-inspired Artificial Intelligence Key Project 2021ZD0202400
6 · The paper itself

Abstract

The interrelation and complementary nature of multi-omics data can provide valuable insights into the intricate molecular mechanisms underlying diseases. However, challenges such as limited sample size, high data dimensionality and differences in omics modalities pose significant obstacles to fully harnessing the potential of these data. The prior knowledge such as gene regulatory network and pathway information harbors useful gene-gene interaction and gene functional module information. To effectively integrate multi-omics data and make full use of the prior knowledge, here, we propose a Multilevel-graph neural network (GNN): a hierarchically designed deep learning algorithm that sequentially leverages multi-omics data, gene regulatory networks and pathway information to extract features and enhance accuracy in predicting survival risk. Our method achieved better accuracy compared with existing methods. Furthermore, key factors nonlinearly associated with the tumor pathogenesis are prioritized by employing two interpretation algorithms (i.e. GNN-Explainer and IGscore) for neural networks, at gene and pathway level, respectively. The top genes and pathways exhibit strong associations with disease in survival analyses, many of which such as SEC61G and CYP27B1 are previously reported in the literature.

Indexed as

AlgorithmsGene Regulatory NetworksNeoplasmsNeural Networks, ComputerComputational BiologyDeep LearningGenomicsHumansMultiomicsgraph neural networkinterpretabilitymulti-omicspathwayrisk classification

Identifiers

PMID38670157
PMCPMC11052635
OpenAlexW4395660270

What OpenQuestion holds

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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.