Identification of relevant subpathways from molecular pathways in gene expression data by a probabilistic approach
Seungyoon Nam
Abstract
Seungyoon Nam
Abstract
High throughput gene expression technologies have been widely used in many biological fields. Typical analysis of gene expression data is to find similarly expressed gene groups by clustering approaches and to identify differentially expressed genes by statistical approaches. The analysis, however, still has a difficulty in interpreting molecular level interaction or signaling transduction based on prior biological information. Recently, a Gene Set Analysis (GSA) approach was developed by a MIT group, which paved the first way for inferring molecular pathway mechanisms behind differentially express genes among sample groups. Current GSA approaches do not take hierarchical regulation among gene entries based on prior pathway information (e.g., KEGG pathways) into consideration. Our proposed approach is that GSA can be expanded not only to reflect the hierarchical structures among genes but also to identify specific subpathways that statistically agree with gene expression data as well as that could explain molecular level mechanism differences between two sample groups. We obtained the KEGG pathways (http://www.genome.jp/kegg/pathway.html) of which nodes and edges were taken into consideration by a probabilistic model. A statistic was calculated for each subpathway in every KEGG pathway based on the model. We identified significant subpathways in an expression dataset.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
High throughput gene expression technologies have been widely used in many biological fields. Typical analysis of gene expression data is to find similarly expressed gene groups by clustering approaches and to identify differentially expressed genes by statistical approaches. The analysis, however, still has a difficulty in interpreting molecular level interaction or signaling transduction based on prior biological information. Recently, a Gene Set Analysis (GSA) approach was developed by a MIT group, which paved the first way for inferring molecular pathway mechanisms behind differentially express genes among sample groups. Current GSA approaches do not take hierarchical regulation among gene entries based on prior pathway information (e.g., KEGG pathways) into consideration. Our proposed approach is that GSA can be expanded not only to reflect the hierarchical structures among genes but also to identify specific subpathways that statistically agree with gene expression data as well as that could explain molecular level mechanism differences between two sample groups. We obtained the KEGG pathways (http://www.genome.jp/kegg/pathway.html) of which nodes and edges were taken into consideration by a probabilistic model. A statistic was calculated for each subpathway in every KEGG pathway based on the model. We identified significant subpathways in an expression dataset.
Key concepts: KEGG, Computational biology, Biological pathway, Gene, Identification (biology), Biology, Gene expression, Bioinformatics