Evidence map›Paper›PMID 34252965›Full record

ArticleBioinformatics (Oxford, England)2021

KG4SL: knowledge graph neural network for synthetic lethality prediction in human cancers.

Shike Wang, Fan Xu, Yunyang Li, Jie Wang, Ke Zhang, Yong Liu, Min Wu, Jie Zheng

Open access · hybridAbstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 1 pooled it
7.2field-weighted citation impact, top 2% 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

40 citing papers in PubMed, 1 synthesis or guideline pooled it, 73 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Target identification and assessment in the era of AI.Nature reviews. Drug discovery · 2026
    Review
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  8. Article
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  15. A Survey on Unifying Large Language Models and Knowledge Graphs for Biomedicine and Healthcare.KDD : proceedings. International Conference on Knowledge Discovery & Data Mining · 2025
    Article
  16. Review
  17. Article
  18. Overview and Prospects of DNA Sequence Visualization.International journal of molecular sciences · 2025
    Review
  19. Machine Learning Approaches for the Identification of Genetic Interactions.Methods in molecular biology (Clifton, N.J.) · 2025
    Review
  20. 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

8 authors at 3 institutions in 2 countries.

Shike WangSchool of Information Science and Technology, ShanghaiTech University, Shanghai 201210, China.
Fan XuSchool of Information Science and Technology, ShanghaiTech University, Shanghai 201210, China.
Yunyang LiSchool of Life Science and Technology, ShanghaiTech University, Shanghai 201210, China.
Jie WangSchool of Information Science and Technology, ShanghaiTech University, Shanghai 201210, China.
Ke ZhangSchool of Information Science and Technology, ShanghaiTech University, Shanghai 201210, China.
Yong LiuJoint NTU-UBC Research Centre of Excellence in Active Living for the Elderly, Nanyang Technological University, Singapore 639798, Singapore.
Min WuInstitute for Infocomm Research, Agency for Science, Technology and Research (A*STAR), Singapore 138632, Singapore.ORCID 0000-0003-0977-3600
Jie ZhengSchool of Information Science and Technology, ShanghaiTech University, Shanghai 201210, China.
ShanghaiTech University · CNAgency for Science, Technology and Research · SGNanyang Technological University · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

motivationSynthetic lethality (SL) is a promising gold mine for the discovery of anti-cancer drug targets. Wet-lab screening of SL pairs is afflicted with high cost, batch-effect, and off-target problems. Current computational methods for SL prediction include gene knock-out simulation, knowledge-based data mining and machine learning methods. Most of the existing methods tend to assume that SL pairs are independent of each other, without taking into account the shared biological mechanisms underlying the SL pairs. Although several methods have incorporated genomic and proteomic data to aid SL prediction, these methods involve manual feature engineering that heavily relies on domain knowledge.

resultsHere, we propose a novel graph neural network (GNN)-based model, named KG4SL, by incorporating knowledge graph (KG) message-passing into SL prediction. The KG was constructed using 11 kinds of entities including genes, compounds, diseases, biological processes and 24 kinds of relationships that could be pertinent to SL. The integration of KG can help harness the independence issue and circumvent manual feature engineering by conducting message-passing on the KG. Our model outperformed all the state-of-the-art baselines in area under the curve, area under precision-recall curve and F1. Extensive experiments, including the comparison of our model with an unsupervised TransE model, a vanilla graph convolutional network model, and their combination, demonstrated the significant impact of incorporating KG into GNN for SL prediction. AVAILABILITY AND IMPLEMENTATION: : KG4SL is freely available at https://github.com/JieZheng-ShanghaiTech/KG4SL. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Indexed as

NeoplasmsSynthetic Lethal MutationsHumansNeural Networks, ComputerPattern Recognition, AutomatedProteomics

Identifiers

PMID34252965
PMCPMC8336442
OpenAlexW3181518724

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.