ArticleJournal of biomedicine & biotechnology2009
Integrating diverse information to gain more insight into microarray analysis.
Article in Journal of biomedicine & biotechnology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
1 citing paper in PubMed, 2 citations in OpenAlex.
- Genomic Copy Number Variation Affecting Genes Involved in the Cell Cycle Pathway: Implications for Somatic Mosaicism.International journal of genomics · 2015Article
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2 authors at 2 institutions in 1 country.
Funding
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Abstract
Microarray technology provides an opportunity to view transcriptions at genomic level under different conditions controlled by an experiment. From an array experiment using a human cancer cell line that is engineered to differ in expression of tumor antigen, integrin alpha6beta4, few hundreds of differentially expressed genes are selected and are clustered using one of several standard algorithms. The set of genes in a cluster is expected to have similar expression patterns and are most likely to be coregulated and thereby expected to have similar function. The highly expressed set of upregulated genes become candidates for further evaluation as potential biomarkers. Besides these benefits, microarray experiment by itself does not help us to understand or discover potential pathways or to identify important set of genes for potential drug targets. In this paper we discuss about integrating protein-to-protein interaction information, pathway information with array expression data set to identify a set of "important" genes, and potential signal transduction networks that help to target and reverse the oncogenic phenotype induced by tumor antigen such as integrin alpha6beta4. We will illustrate the proposed method with our recent microarray experiment conducted for identifying transcriptional targets of integrin alpha6beta4 for cancer progression.
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Registered trials
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