Evidence map›Paper›PMID 18564431›Full record

ArticleBMC bioinformatics2008

Genome-scale cluster analysis of replicated microarrays using shrinkage correlation coefficient.

Jianchao Yao, Chunqi Chang, Mari L Salmi, Yeung Sam Hung, Ann Loraine, Stanley J Roux

Abstract read
In one paragraph

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 13 papers.

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0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Jianchao YaoInstitute for Cellular and Molecular Biology and Department of Mathematics, University of Texas at Austin, Austin, Texas 78712, USA. jcyao@mail.utexas.edu
Chunqi Chang
Mari L Salmi
Yeung Sam Hung
Ann Loraine
Stanley J Roux

Funding

Beta Amyloid and Presynaptic Nicotinic ReceptorsR01AG021586 · NIA · UNIVERSITY OF HAWAII AT MANOA · PI NICHOLS, ROBERT ALAN · 2004 to 2007
$887k
NIA NIH HHS R01 AG021586
6 · The paper itself

Abstract

backgroundCurrently, clustering with some form of correlation coefficient as the gene similarity metric has become a popular method for profiling genomic data. The Pearson correlation coefficient and the standard deviation (SD)-weighted correlation coefficient are the two most widely-used correlations as the similarity metrics in clustering microarray data. However, these two correlations are not optimal for analyzing replicated microarray data generated by most laboratories. An effective correlation coefficient is needed to provide statistically sufficient analysis of replicated microarray data.

resultsIn this study, we describe a novel correlation coefficient, shrinkage correlation coefficient (SCC), that fully exploits the similarity between the replicated microarray experimental samples. The methodology considers both the number of replicates and the variance within each experimental group in clustering expression data, and provides a robust statistical estimation of the error of replicated microarray data. The value of SCC is revealed by its comparison with two other correlation coefficients that are currently the most widely-used (Pearson correlation coefficient and SD-weighted correlation coefficient) using statistical measures on both synthetic expression data as well as real gene expression data from Saccharomyces cerevisiae. Two leading clustering methods, hierarchical and k-means clustering were applied for the comparison. The comparison indicated that using SCC achieves better clustering performance. Applying SCC-based hierarchical clustering to the replicated microarray data obtained from germinating spores of the fern Ceratopteris richardii, we discovered two clusters of genes with shared expression patterns during spore germination. Functional analysis suggested that some of the genetic mechanisms that control germination in such diverse plant lineages as mosses and angiosperms are also conserved among ferns.

conclusionThis study shows that SCC is an alternative to the Pearson correlation coefficient and the SD-weighted correlation coefficient, and is particularly useful for clustering replicated microarray data. This computational approach should be generally useful for proteomic data or other high-throughput analysis methodology.

Indexed as

ProbabilityArtificial IntelligenceCluster AnalysisComputational BiologyComputer SimulationConfidence IntervalsGene ExpressionGene Expression ProfilingGenomicsGerminationOligonucleotide Array Sequence AnalysisPteridaceaeResearch DesignSaccharomyces cerevisiae

Identifiers

PMID18564431
PMCPMC2459189

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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.