Evidence map›Paper›PMID 23368633›Full record

ArticleBMC genomics2013

A genome-wide cis-regulatory element discovery method based on promoter sequences and gene co-expression networks.

Zhen Gao, Ruizhe Zhao, Jianhua Ruan

Abstract read
In one paragraph

Article in BMC genomics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

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0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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3 · Its place in the literature

Who cites it

6 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.

Zhen GaoDepartment of Computer Science, The University of Texas at San Antonio, One UTSA Circle, San Antonio, TX 78249, USA. zgao@cs.utsa.edu
Ruizhe Zhao
Jianhua Ruan

Funding

Predicting Drug Resistance in Cancer Genomes by DMA Methylation ProfilingU54CA113001 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI HUANG, TIM H.-M. · 2004 to 2014
$16.1M
RCMI Center for Interdiscplinary Health Research CIHRG12MD007591 · NIMHD · UNIVERSITY OF TEXAS SAN ANTONIO · PI PERRY, GEORGE · 2012 to 2016
$10.4M
Computational Discovery and Analysis of Community Structures in Biology NetworksSC3GM086305 · NIGMS · UNIVERSITY OF TEXAS SAN ANTONIO · PI RUAN, JIANHUA · 2009 to 2012
$555k
NCI NIH HHS U54CA113001NIGMS NIH HHS SC3 GM086305NIGMS NIH HHS SC3GM086305NIMHD NIH HHS G12 MD007591NIMHD NIH HHS G12MD007591
6 · The paper itself

Abstract

backgroundDeciphering cis-regulatory networks has become an attractive yet challenging task. This paper presents a simple method for cis-regulatory network discovery which aims to avoid some of the common problems of previous approaches.

resultsUsing promoter sequences and gene expression profiles as input, rather than clustering the genes by the expression data, our method utilizes co-expression neighborhood information for each individual gene, thereby overcoming the disadvantages of current clustering based models which may miss specific information for individual genes. In addition, rather than using a motif database as an input, it implements a simple motif count table for each enumerated k-mer for each gene promoter sequence. Thus, it can be used for species where previous knowledge of cis-regulatory motifs is unknown and has the potential to discover new transcription factor binding sites. Applications on Saccharomyces cerevisiae and Arabidopsis have shown that our method has a good prediction accuracy and outperforms a phylogenetic footprinting approach. Furthermore, the top ranked gene-motif regulatory clusters are evidently functionally co-regulated, and the regulatory relationships between the motifs and the enriched biological functions can often be confirmed by literature.

conclusionsSince this method is simple and gene-specific, it can be readily utilized for insufficiently studied species or flexibly used as an additional step or data source for previous transcription regulatory networks discovery models.

Indexed as

Genome, FungalGenome, PlantArabidopsisCluster AnalysisComputational BiologyGene Expression ProfilingGene Regulatory NetworksMultigene FamilyPromoter Regions, GeneticSaccharomyces cerevisiaeTranscription FactorsTranscription Factors

Identifiers

PMID23368633
PMCPMC3549801

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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.