Evidence map›Paper›PMID 34419588›Full record

ArticleMethods (San Diego, Calif.)2022

Heterogeneous graph attention networks for drug virus association prediction.

Yahui Long, Yu Zhang, Min Wu, Shaoliang Peng, Chee Keong Kwoh, Jiawei Luo, Xiaoli Li

Open access · greenAbstract read
In one paragraph

Article in Methods (San Diego, Calif.), 2022. 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
2.4field-weighted citation impact, top 10% 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

7 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. Proceedings of machine learning research · 2024
    Article
  4. Article
  5. Article
  6. A geometric deep learning model for display and prediction of potential drug-virus interactions against SARS-CoV-2.Chemometrics and intelligent laboratory systems : an international journal sponsored by the Chemometrics Society · 2022
    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

7 authors at 4 institutions in 2 countries.

Yahui LongCollege of Computer Science and Electronic Engineering, Hunan University, Changsha 410000, China; School of Computer Science and Engineering, Nanyang Technological University, Singapore 639798, Singapore.
Yu ZhangSchool of Computer Science and Engineering, Nanyang Technological University, Singapore 639798, Singapore.
Min WuInstitute for Infocomm Research, Agency for Science, Technology and Research (A*STAR), 138632, Singapore.
Shaoliang PengCollege of Computer Science and Electronic Engineering, Hunan University, Changsha 410000, China.
Chee Keong KwohSchool of Computer Science and Engineering, Nanyang Technological University, Singapore 639798, Singapore.
Jiawei LuoCollege of Computer Science and Electronic Engineering, Hunan University, Changsha 410000, China. Electronic address: luojiawei@hnu.edu.cn.
Xiaoli LiInstitute for Infocomm Research, Agency for Science, Technology and Research (A*STAR), 138632, Singapore. Electronic address: xlli@i2r.a-star.edu.sg.
Hunan University · CNNanyang Technological University · SGAgency for Science, Technology and Research · SGInstitute for Infocomm Research · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Coronavirus Disease-19 (COVID-19) has lead global epidemics with high morbidity and mortality. However, there are currently no proven effective drugs targeting COVID-19. Identifying drug-virus associations can not only provide insights into the understanding of drug-virus interaction mechanism, but also guide and facilitate the screening of compound candidates for antiviral drug discovery. Since conventional experiment methods are time-consuming, laborious and expensive, computational methods to identify potential drug candidates for viruses (e.g., COVID-19) provide an alternative strategy. In this work, we propose a novel framework of Heterogeneous Graph Attention Networks for Drug-Virus Association predictions, named HGATDVA. First, we fully incorporate multiple sources of biomedical data, e.g., drug chemical information, virus genome sequences and viral protein sequences, to construct abundant features for drugs and viruses. Second, we construct two drug-virus heterogeneous graphs. For each graph, we design a self-enhanced graph attention network (SGAT) to explicitly model the dependency between a node and its local neighbors and derive the graph-specific representations for nodes. Third, we further develop a neural network architecture with tri-aggregator to aggregate the graph-specific representations to generate the final node representations. Extensive experiments were conducted on two datasets, i.e., DrugVirus and MDAD, and the results demonstrated that our model outperformed 7 state-of-the-art methods. Case study on SARS-CoV-2 validated the effectiveness of our model in identifying potential drugs for viruses.

Indexed as

COVID-19Pharmaceutical PreparationsDrug InteractionsHumansNeural Networks, ComputerSARS-CoV-2Pharmaceutical PreparationsAssociation predictionCOVID-19DrugHeterogeneous graph attention networksSARS-CoV-2

Identifiers

PMID34419588
PMCPMC8376526
OpenAlexW3194220893

What OpenQuestion holds

Textmetadata
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.