Evidence map›Paper›PMID 31060502›Full record

ArticleBMC bioinformatics2019

GeneSurrounder: network-based identification of disease genes in expression data.

Sahil D Shah, Rosemary Braun

Open access · goldAbstract read
In one paragraph

Article in BMC bioinformatics, 2019. 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
0.4field-weighted citation impact, top 38% 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, 11 citations in OpenAlex.

  1. Article
  2. Transcription-based comparison ofMicrobiology spectrum · 2026
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  3. Article
  4. Network analysis of driver genes in human cancers.Frontiers in bioinformatics · 2024
    Article
  5. Article
  6. 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

2 authors at 1 institution in 1 country.

Sahil D ShahEngineering Sciences and Applied Mathematics, Northwestern University, Evanston, USA.ORCID http://orcid.org/0000-0002-7644-1166
Rosemary BraunEngineering Sciences and Applied Mathematics, Northwestern University, Evanston, USA. rbraun@northwestern.edu.
Northwestern University · US

Funding

Multiscale Modeling of Myelodysplastic SyndromesR01HL128173 · NHLBI · VIRGINIA COMMONWEALTH UNIVERSITY · PI COREY, SETH JOEL, KIMMEL, MAREK · 2015 to 2019
$3.8M
James S. McDonnell Foundation (US) 220020394National Heart, Lung, and Blood Institute (US) R01HL128173NHLBI NIH HHS R01 HL128173
6 · The paper itself

Abstract

backgroundA key challenge of identifying disease-associated genes is analyzing transcriptomic data in the context of regulatory networks that control cellular processes in order to capture multi-gene interactions and yield mechanistically interpretable results. One existing category of analysis techniques identifies groups of related genes using interaction networks, but these gene sets often comprise tens or hundreds of genes, making experimental follow-up challenging. A more recent category of methods identifies precise gene targets while incorporating systems-level information, but these techniques do not determine whether a gene is a driving source of changes in its network, an important characteristic when looking for potential drug targets.

resultsWe introduce GeneSurrounder, an analysis method that integrates expression data and network information in a novel procedure to detect genes that are sources of dysregulation on the network. The key idea of our method is to score genes based on the evidence that they influence the dysregulation of their neighbors on the network in a manner that impacts cell function. Applying GeneSurrounder to real expression data, we show that our method is able to identify biologically relevant genes, integrate pathway and expression data, and yield more reproducible results across multiple studies of the same phenotype than competing methods.

conclusionsTogether these findings suggest that GeneSurrounder provides a new avenue for identifying individual genes that can be targeted therapeutically. The key innovation of GeneSurrounder is the combination of pathway network information with gene expression data to determine the degree to which a gene is a source of dysregulation on the network. By prioritizing genes in this way, our method provides insights into disease mechanisms and suggests diagnostic and therapeutic targets. Our method can be used to help biologists select among tens or hundreds of genes for further validation. The implementation in R is available at github.com/sahildshah1/gene-surrounder.

Indexed as

AlgorithmsComputational BiologyGene ExpressionGene Regulatory NetworksHumansAlgorithmsGene expressionNetworksPathwaysSystems biology

Identifiers

PMID31060502
PMCPMC6503437
OpenAlexW2945138188

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.