| Literature DB >> 25984395 |
Julian Dymacek1, Nancy Lan Guo1.
Abstract
This study presents a novel computational approach to find relevant pathways from dose-dependent time series gene expression data which are significantly associated with a phenotype pattern pathological patterns in the comprehensive evaluation of database of pathways. Our system uses four steps: 1) identify a set of genes which change significantly in dose or time; 2) find phenotype patterns and gene coefficients for the genes found in step 1; 3) expand to genome-wide coefficients, and 4) identify pathways which are significantly relevant to a phenotype pattern. Our technique finds biologically relevant pathways with and without phenotype-constraints. Our system has been used on genome-wide expression profiles of mouse lungs (n=160) following aspiration of well dispersed multi-walled carbon nanotubes (MWCNT), in order to detect MWCNT-induced lung inflammation and related pathways. The identified significant pathways are supported by evidence in the literature and biological validation.Entities:
Keywords: dose-dependent time series microarray data; nanoparticles; pathways; toxicogenomics
Year: 2011 PMID: 25984395 PMCID: PMC4429298 DOI: 10.1109/BIBM.2011.76
Source DB: PubMed Journal: Proceedings (IEEE Int Conf Bioinformatics Biomed) ISSN: 2156-1125