Evidence map›Paper›PMID 18433478›Full record

ArticleBMC bioinformatics2008

Identification of coherent patterns in gene expression data using an efficient biclustering algorithm and parallel coordinate visualization.

Kin-On Cheng, Ngai-Fong Law, Wan-Chi Siu, Alan Wee-Chung Liew

Abstract read
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Article in BMC bioinformatics, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

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15citing papers in PubMed
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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

15 citing papers in PubMed.

  1. RUBic: rapid unsupervised biclustering.BMC bioinformatics · 2023
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  12. Mining functionally relevant gene sets for analyzing physiologically novel clinical expression data.Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing · 2011
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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Kin-On ChengSchool of Information and Communication Technology, Griffith University, Gold Coast Campus, QLD 4222, Queensland, Australia. k.o.cheng@polyu.edu.hk
Ngai-Fong Law
Wan-Chi Siu
Alan Wee-Chung Liew

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe DNA microarray technology allows the measurement of expression levels of thousands of genes under tens/hundreds of different conditions. In microarray data, genes with similar functions usually co-express under certain conditions only 1. Thus, biclustering which clusters genes and conditions simultaneously is preferred over the traditional clustering technique in discovering these coherent genes. Various biclustering algorithms have been developed using different bicluster formulations. Unfortunately, many useful formulations result in NP-complete problems. In this article, we investigate an efficient method for identifying a popular type of biclusters called additive model. Furthermore, parallel coordinate (PC) plots are used for bicluster visualization and analysis.

resultsWe develop a novel and efficient biclustering algorithm which can be regarded as a greedy version of an existing algorithm known as pCluster algorithm. By relaxing the constraint in homogeneity, the proposed algorithm has polynomial-time complexity in the worst case instead of exponential-time complexity as in the pCluster algorithm. Experiments on artificial datasets verify that our algorithm can identify both additive-related and multiplicative-related biclusters in the presence of overlap and noise. Biologically significant biclusters have been validated on the yeast cell-cycle expression dataset using Gene Ontology annotations. Comparative study shows that the proposed approach outperforms several existing biclustering algorithms. We also provide an interactive exploratory tool based on PC plot visualization for determining the parameters of our biclustering algorithm.

conclusionWe have proposed a novel biclustering algorithm which works with PC plots for an interactive exploratory analysis of gene expression data. Experiments show that the biclustering algorithm is efficient and is capable of detecting co-regulated genes. The interactive analysis enables an optimum parameter determination in the biclustering algorithm so as to achieve the best result. In future, we will modify the proposed algorithm for other bicluster models such as the coherent evolution model.

Indexed as

AlgorithmsCluster AnalysisComputer GraphicsUser-Computer InterfaceArtificial IntelligenceGene Expression ProfilingOligonucleotide Array Sequence AnalysisPattern Recognition, AutomatedProgramming Languages

Identifiers

PMID18433478
PMCPMC2396181

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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.