Evidence map›Paper›PMID 33726666›Full record

ArticleBMC bioinformatics2021

Juxtapose: a gene-embedding approach for comparing co-expression networks.

Katie Ovens, Farhad Maleki, B Frank Eames, Ian McQuillan

Abstract read
In one paragraph

Article in BMC bioinformatics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Biclustering data analysis: a comprehensive survey.Briefings in bioinformatics · 2024
    Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Translational Informatics for Natural Products as Antidepressant Agents.Frontiers in cell and developmental biology · 2021
    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

4 authors.

Katie OvensDepartment of Computer Science, University of Saskatchewan, Saskatoon, S7N 5C9, Canada. katie.ovens@usask.ca.ORCID http://orcid.org/0000-0001-5956-7739
Farhad MalekiAugmented Intelligence & Precision Health Laboratory (AIPHL), Research Institute of the McGill University Health Centre, Montreal, H4A 3S5, Canada.
B Frank EamesDepartment of Anatomy, Physiology, and Pharmacology, University of Saskatchewan, Saskatoon, S7N 5E5, Canada.
Ian McQuillanDepartment of Computer Science, University of Saskatchewan, Saskatoon, S7N 5C9, Canada.

Funding

Natural Sciences and Engineering Research Council of Canada 2016-06172Natural Sciences and Engineering Research Council of Canada 2019-05977Natural Sciences and Engineering Research Council of Canada 435655-201
6 · The paper itself

Abstract

backgroundGene co-expression networks (GCNs) are not easily comparable due to their complex structure. In this paper, we propose a tool, Juxtapose, together with similarity measures that can be utilized for comparative transcriptomics between a set of organisms. While we focus on its application to comparing co-expression networks across species in evolutionary studies, Juxtapose is also generalizable to co-expression network comparisons across tissues or conditions within the same species.

methodsA word embedding strategy commonly used in natural language processing was utilized in order to generate gene embeddings based on walks made throughout the GCNs. Juxtapose was evaluated based on its ability to embed the nodes of synthetic structures in the networks consistently while also generating biologically informative results. Evaluation of the techniques proposed in this research utilized RNA-seq datasets from GTEx, a multi-species experiment of prefrontal cortex samples from the Gene Expression Omnibus, as well as synthesized datasets. Biological evaluation was performed using gene set enrichment analysis and known gene relationships in literature.

resultsWe show that Juxtapose is capable of globally aligning synthesized networks as well as identifying areas that are conserved in real gene co-expression networks without reliance on external biological information. Furthermore, output from a matching algorithm that uses cosine distance between GCN embeddings is shown to be an informative measure of similarity that reflects the amount of topological similarity between networks.

conclusionsJuxtapose can be used to align GCNs without relying on known biological similarities and enables post-hoc analyses using biological parameters, such as orthology of genes, or conserved or variable pathways. AVAILABILITY: A development version of the software used in this paper is available at https://github.com/klovens/juxtapose.

Indexed as

Computational BiologyGene Regulatory NetworksAlgorithmsSoftwareEmbeddingEvolutionGene co-expression networksMachine learningTranscriptomicsWord2vec

Identifiers

PMID33726666
PMCPMC7968242

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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.