Evidence map›Paper›PMID 31074376›Full record

ArticleBMC bioinformatics2019

Generalized gene co-expression analysis via subspace clustering using low-rank representation.

Tongxin Wang, Jie Zhang, Kun Huang

Abstract 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 4 papers.

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4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Tongxin WangDepartment of Computer Science, Indiana University Bloomington, Bloomington, 47408, IN, USA.
Jie ZhangDepartment of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, 46202, IN, USA.
Kun HuangDepartment of Medicine, Indiana University School of Medicine, Indianapolis, 46202, IN, USA. kunhuang@iu.edu.

Funding

Informatics Links Between Histological Features and Genetics in CancerU01CA188547 · NCI · OHIO STATE UNIVERSITY · PI HUANG, KUN · 2015 to 2017
$1.2M
NCI NIH HHS U01 CA188547
6 · The paper itself

Abstract

backgroundGene Co-expression Network Analysis (GCNA) helps identify gene modules with potential biological functions and has become a popular method in bioinformatics and biomedical research. However, most current GCNA algorithms use correlation to build gene co-expression networks and identify modules with highly correlated genes. There is a need to look beyond correlation and identify gene modules using other similarity measures for finding novel biologically meaningful modules.

resultsWe propose a new generalized gene co-expression analysis algorithm via subspace clustering that can identify biologically meaningful gene co-expression modules with genes that are not all highly correlated. We use low-rank representation to construct gene co-expression networks and local maximal quasi-clique merger to identify gene co-expression modules. We applied our method on three large microarray datasets and a single-cell RNA sequencing dataset. We demonstrate that our method can identify gene modules with different biological functions than current GCNA methods and find gene modules with prognostic values.

conclusionsThe presented method takes advantage of subspace clustering to generate gene co-expression networks rather than using correlation as the similarity measure between genes. Our generalized GCNA method can provide new insights from gene expression datasets and serve as a complement to current GCNA algorithms.

Indexed as

Gene Expression Regulation, NeoplasticGene Regulatory NetworksAlgorithmsCluster AnalysisComputational BiologyGene Expression ProfilingHumansNeoplasm ProteinsNeoplasmsNeoplasm ProteinsGene co-expression network analysisLow-rank representationSubspace clustering

Identifiers

PMID31074376
PMCPMC6509871

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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.