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Dammer, L.

Publications and source records attributed to Dammer, L..

2 recordsLinked to original sources

GeDi: Simplifying Gene Set Distances for Enhanced Omics Interpretation in R/Bioconductor

BackgroundFunctional enrichment analysis is a standard component in many omics data analysis workflows, supported by a variety of methods and algorithms. However, despite their utility and wide application, these methods often return the results as an extensive and redundant list of gene sets, impeding interpretation and hypothesis generation. Moreover, network based information can provide additional biological context through functional interaction data, yet this is often overlooked by existing tools. ResultsWe developed GeDi, an R/Bioconductor package designed to streamline and standardize the interpretation of functional enrichment results. GeDi aggregates gene sets into biologically meaningful clusters using a suite of gene set distance metrics and clustering algorithms, aimed to reduce redundancy and improve clarity. GeDi also enables the integration of protein-protein interaction (PPI) data, through the implementation of a weighted distance metric, providing a richer biological context by capturing functional connectivity between pathways and their components. The package offers visualizations, aggregation, and automated reporting, and is available as both a stand-alone R-package and an interactive Shiny application. ConclusionGeDi facilitates clearer, faster interpretation of enrichment results by combining clustering and network context. Application to a public RNA-seq dataset revealed coherent biological themes, supporting both experimental and computational research. GeDi is freely available in the Bioconductor project under the MIT license (https://bioconductor.org/packages/GeDi), and a demo instance is accessible on the Shiny server (http://shiny.imbei.uni-mainz.de:3838/GeDi).

bioinformatics↗

Adaptation of the Spalax galili transcriptome to life under hypoxia may hold a key to a complex phenotype including longevity and cancer resistance

The muroid rodent Nannospalax galili (syn. Spalax) is adapted to life in underground burrows and tolerates acute exposure to severe hypoxia. Adaptation to hypoxia is correlated with delayed onset of ageing and resistance against tumour formation. Spalax becomes five to seven times older than its relatives, the mouse and rat, without displaying signs of ageing or developing ageing-related disorders like cancer. Investigating and understanding adapted genes and gene regulatory networks of Spalax might pinpoint novel strategies to maintain an extended healthy phenotype in humans. Here we analysed and compared RNA-Seq data of liver, kidney and spleen of Spalax and rat subjected to 6% O2 or normoxia. We identified differentially expressed genes and pathways common to multiple organs in Spalax and rat. Body-wide differences between Spalax and rat affected biological processes like cell death, defence against reactive oxygen species (ROS), DNA repair, energy metabolism, immune response and angiogenesis, which altogether might play a crucial role in Spalaxs adaptation to life under oxygen deprivation. In all organs, mRNA expression of genes associated with genome stability maintenance and DNA repair was elevated in Spalax compared to rat, accompanied by a lower gene expression of genes associated with aerobic energy metabolism and proinflammatory processes. These transcriptomic changes might be accountable for the extraordinary lifespan of Spalax and its cancer resistance. Our results reveal gene regulatory networks that become candidates for the investigation of the molecular bases that underlie the complex phenotype of Spalax.

evolutionary biology↗