Evidence map›Paper›PMID 36688699›Full record

ArticleBioinformatics (Oxford, England)2023

Accurately modeling biased random walks on weighted networks using node2vec.

Renming Liu, Matthew Hirn, Arjun Krishnan

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Molecular maps of diseases from omics data and network embeddings.NPJ systems biology and applications · 2026
    Article
  2. Article
  3. Review
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  5. SPACE: STRING proteins as complementary embeddings.Bioinformatics (Oxford, England) · 2025
    Article
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  12. Review
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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

3 authors.

Renming LiuDepartment of Computational Mathematics, Science & Engineering, Michigan State University, East Lansing, MI 48824, USA.ORCID 0000-0002-6025-6492
Matthew HirnDepartment of Computational Mathematics, Science & Engineering, Michigan State University, East Lansing, MI 48824, USA.ORCID 0000-0003-0290-4292
Arjun KrishnanDepartment of Computational Mathematics, Science & Engineering, Michigan State University, East Lansing, MI 48824, USA.ORCID 0000-0002-7980-4110

Funding

Resolving and understanding the genomic basis of heterogeneous complex traits and diseasesR35GM128765 · NIGMS · UNIVERSITY OF COLORADO DENVER · PI KRISHNAN, ARJUN · 2018 to 2022
$2.0M
Finding emergent structure in multi-sample biological data with the dual geometry of cells and features R01GM135929 · NIGMS · MICHIGAN STATE UNIVERSITY · PI BROWN, EDWARD · 2019 to 2022
$1.4M
NIGMS NIH HHS R01 GM135929NIGMS NIH HHS R35 GM128765NSF
6 · The paper itself

Abstract

motivationAccurately representing biological networks in a low-dimensional space, also known as network embedding, is a critical step in network-based machine learning and is carried out widely using node2vec, an unsupervised method based on biased random walks. However, while many networks, including functional gene interaction networks, are dense, weighted graphs, node2vec is fundamentally limited in its ability to use edge weights during the biased random walk generation process, thus under-using all the information in the network.

resultsHere, we present node2vec+, a natural extension of node2vec that accounts for edge weights when calculating walk biases and reduces to node2vec in the cases of unweighted graphs or unbiased walks. Using two synthetic datasets, we empirically show that node2vec+ is more robust to additive noise than node2vec in weighted graphs. Then, using genome-scale functional gene networks to solve a wide range of gene function and disease prediction tasks, we demonstrate the superior performance of node2vec+ over node2vec in the case of weighted graphs. Notably, due to the limited amount of training data in the gene classification tasks, graph neural networks such as GCN and GraphSAGE are outperformed by both node2vec and node2vec+. AVAILABILITY AND IMPLEMENTATION: The data and code are available on GitHub at https://github.com/krishnanlab/node2vecplus_benchmarks. All additional data underlying this article are available on Zenodo at https://doi.org/10.5281/zenodo.7007164. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Indexed as

Machine LearningNeural Networks, ComputerEpistasis, GeneticGene Regulatory NetworksPhenotype

Identifiers

PMID36688699
PMCPMC9891245

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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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.