Evidence map›Paper›PMID 37976327›Full record

ArticlePLoS computational biology2023

Gene communities in co-expression networks across different tissues.

Madison Russell, Alber Aqil, Marie Saitou, Omer Gokcumen, Naoki Masuda

Abstract read
In one paragraph

Article in PLoS computational biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Computational modelling of cell identity.The Biochemical journal · 2026
    Review
  5. Article
  6. Article
  7. Article
  8. Spatial Modularity of Innate Immune Networks Across Bactrian Camel Tissues.Animals : an open access journal from MDPI · 2025
    Article
  9. Read mismapping from segmental duplications drives spuriousbioRxiv : the preprint server for biology · 2025
    Article
  10. Article
  11. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Madison RussellDepartment of Mathematics, State University of New York at Buffalo, Buffalo, New York, United States of America.ORCID 0009-0007-6337-3735
Alber AqilDepartment of Biological Sciences, State University of New York at Buffalo, Buffalo, New York, United States of America.
Marie SaitouFaculty of Biosciences, Norwegian University of Life Sciences, Ås, Norway.
Omer GokcumenDepartment of Biological Sciences, State University of New York at Buffalo, Buffalo, New York, United States of America.
Naoki MasudaDepartment of Mathematics, State University of New York at Buffalo, Buffalo, New York, United States of America.ORCID 0000-0003-1567-801X

Funding

DMS/NIGMS 1: Multilayer network approach to tandem repeat variation in genomesR01GM148973 · NIGMS · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI MASUDA, NAOKI · 2022 to 2024
$444k
NIGMS NIH HHS R01 GM148973
6 · The paper itself

Abstract

With the recent availability of tissue-specific gene expression data, e.g., provided by the GTEx Consortium, there is interest in comparing gene co-expression patterns across tissues. One promising approach to this problem is to use a multilayer network analysis framework and perform multilayer community detection. Communities in gene co-expression networks reveal groups of genes similarly expressed across individuals, potentially involved in related biological processes responding to specific environmental stimuli or sharing common regulatory variations. We construct a multilayer network in which each of the four layers is an exocrine gland tissue-specific gene co-expression network. We develop methods for multilayer community detection with correlation matrix input and an appropriate null model. Our correlation matrix input method identifies five groups of genes that are similarly co-expressed in multiple tissues (a community that spans multiple layers, which we call a generalist community) and two groups of genes that are co-expressed in just one tissue (a community that lies primarily within just one layer, which we call a specialist community). We further found gene co-expression communities where the genes physically cluster across the genome significantly more than expected by chance (on chromosomes 1 and 11). This clustering hints at underlying regulatory elements determining similar expression patterns across individuals and cell types. We suggest that KRTAP3-1, KRTAP3-3, and KRTAP3-5 share regulatory elements in skin and pancreas. Furthermore, we find that CELA3A and CELA3B share associated expression quantitative trait loci in the pancreas. The results indicate that our multilayer community detection method for correlation matrix input extracts biologically interesting communities of genes.

Indexed as

Gene Regulatory NetworksQuantitative Trait LociHumansPancreatic ElastaseCELA3B protein, humanPancreatic Elastase

Identifiers

PMID37976327
PMCPMC10691702

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Registered trials

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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.