Evidence map›Paper›PMID 22369275›Full record

ArticleBMC genomics2011

Extracting regulatory modules from gene expression data by sequential pattern mining.

Mingoo Kim, Hyunjung Shin, Tae Su Chung, Je-Gun Joung, Ju Han Kim

Abstract read
In one paragraph

Article in BMC genomics, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

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4 · The record

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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

5 authors.

Mingoo KimSeoul National University Biomedical Informatics, Seoul National University College of Medicine, Seoul 110799, Korea.
Hyunjung Shin
Tae Su Chung
Je-Gun Joung
Ju Han Kim

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIdentifying a regulatory module (RM), a bi-set of co-regulated genes and co-regulating conditions (or samples), has been an important challenge in functional genomics and bioinformatics. Given a microarray gene-expression matrix, biclustering has been the most common method for extracting RMs. Among biclustering methods, order-preserving biclustering by a sequential pattern mining technique has native advantage over the conventional biclustering approaches since it preserves the order of genes (or conditions) according to the magnitude of the expression value. However, previous sequential pattern mining-based biclustering has several weak points in that they can easily be computationally intractable in the real-size of microarray data and sensitive to inherent noise in the expression value.

resultsIn this paper, we propose a novel sequential pattern mining algorithm that is scalable in the size of microarray data and robust with respect to noise. When applied to the microarray data of yeast, the proposed algorithm successfully found long order-preserving patterns, which are biologically significant but cannot be found in randomly shuffled data. The resulting patterns are well enriched to known annotations and are consistent with known biological knowledge. Furthermore, RMs as well as inter-module relations were inferred from the biologically significant patterns.

conclusionsOur approach for identifying RMs could be valuable for systematically revealing the mechanism of gene regulation at a genome-wide level.

Indexed as

AlgorithmsData MiningGene Expression RegulationDatabases, GeneticOligonucleotide Array Sequence AnalysisSaccharomyces cerevisiae

Identifiers

PMID22369275
PMCPMC3333188

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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.