| Literature DB >> 25708305 |
Scott E Nixon1, Dianelys González-Peña, Marcus A Lawson, Robert H McCusker, Alvaro G Hernandez, Jason C O'Connor, Robert Dantzer, Keith W Kelley, Sandra L Rodriguez-Zas.
Abstract
Comprehensive and simultaneous analysis of all genes in a biological sample is a capability of RNA-Seq technology. Analysis of the entire transcriptome benefits from summarization of genes at the functional level. As a cellular response of interest not previously explored with RNA-Seq, peritoneal macrophages from mice under two conditions (control and immunologically challenged) were analyzed for gene expression differences. Quantification of individual transcripts modeled RNA-Seq read distribution and uncertainty (using a Beta Negative Binomial distribution), then tested for differential transcript expression (False Discovery Rate-adjusted p-value < 0.05). Enrichment of functional categories utilized the list of differentially expressed genes. A total of 2079 differentially expressed transcripts representing 1884 genes were detected. Enrichment of 92 categories from Gene Ontology Biological Processes and Molecular Functions, and KEGG pathways were grouped into 6 clusters. Clusters included defense and inflammatory response (Enrichment Score = 11.24) and ribosomal activity (Enrichment Score = 17.89). Our work provides a context to the fine detail of individual gene expression differences in murine peritoneal macrophages during immunological challenge with high throughput RNA-Seq.Entities:
Keywords: RNA-Seq; functional analysis; macrophage; transcriptome
Mesh:
Year: 2015 PMID: 25708305 PMCID: PMC4539142 DOI: 10.1142/S0219720015500109
Source DB: PubMed Journal: J Bioinform Comput Biol ISSN: 0219-7200 Impact factor: 1.122