Evidence map›Paper›PMID 34743699›Full record

ArticleBMC bioinformatics2021

Identifying stress responsive genes using overlapping communities in co-expression networks.

Camila Riccio-Rengifo, Jorge Finke, Camilo Rocha

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 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

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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.

Camila Riccio-RengifoDepartment of Natural Sciences and Mathematics, Pontificia Universidad Javeriana, Cali, Colombia. camila.riccio@javerianacali.edu.co.ORCID http://orcid.org/0000-0002-3945-7820
Jorge FinkeDepartment of Electronics and Computer Science, Pontificia Universidad Javeriana, Cali, Colombia.
Camilo RochaDepartment of Electronics and Computer Science, Pontificia Universidad Javeriana, Cali, Colombia.

Funding

World Bank Group FP44842-217-2018
6 · The paper itself

Abstract

backgroundThis paper proposes a workflow to identify genes that respond to specific treatments in plants. The workflow takes as input the RNA sequencing read counts and phenotypical data of different genotypes, measured under control and treatment conditions. It outputs a reduced group of genes marked as relevant for treatment response. Technically, the proposed approach is both a generalization and an extension of WGCNA. It aims to identify specific modules of overlapping communities underlying the co-expression network of genes. Module detection is achieved by using Hierarchical Link Clustering. The overlapping nature of the systems' regulatory domains that generate co-expression can be identified by such modules. LASSO regression is employed to analyze phenotypic responses of modules to treatment.

resultsThe workflow is applied to rice (Oryza sativa), a major food source known to be highly sensitive to salt stress. The workflow identifies 19 rice genes that seem relevant in the response to salt stress. They are distributed across 6 modules: 3 modules, each grouping together 3 genes, are associated to shoot K content; 2 modules of 3 genes are associated to shoot biomass; and 1 module of 4 genes is associated to root biomass. These genes represent target genes for the improvement of salinity tolerance in rice.

conclusionsA more effective framework to reduce the search-space for target genes that respond to a specific treatment is introduced. It facilitates experimental validation by restraining efforts to a smaller subset of genes of high potential relevance.

Indexed as

OryzaGenotypeSalt ToleranceSequence Analysis, RNAStress, PhysiologicalCo-expression networkLASSOOryza sativaOverlapping communitiesPhenotypic traitsRiceSalinityStress-responsive genes

Identifiers

PMID34743699
PMCPMC8574028

What OpenQuestion holds

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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.