Search bioRxiv⌕ Search

bioRxiv · 10.1101/2023.06.30.547164

Concise functional enrichment of ranked gene lists

Abstract

Genome-wide expression data has become ubiquitous within the last two decades. Given such data, functional enrichment methods identify functional categories (e.g., biological processes) that preferentially annotate differentially expressed genes. However, many existing methods operate in a binary manner, disregarding valuable information contained in the gene ranking. The few methods that consider the ranking often return redundant or non-specific functional categories. To address these limitations, we developed a novel method called Concise Ranked Functional Enrichment (CRFE), which effectively leverages the ranking information in gene expression data to compute a non-redundant set of specific functional categories that are notably enriched for highly ranked genes. A particularly useful feature of CRFE is a tunable parameter that defines how much focus should be given to the most highly ranked genes. Using four treatment-control RNA-seq datasets, we compared the performance of CRFE with the two most widely used types of functional enrichment methods, Gene Set Enrichment Analysis and over-representation analysis. We evaluated the methods based on their ability to utilize ranking information, generate non-redundant results, and return functional categories with high information content. CRFE excelled in all evaluated criteria, outperforming the existing methods, each of which exhibits deficiencies in at least one aspect. Using lung adenocarcinoma data, we further showed that the functional categories identified by CRFE are biologically meaningful. In conclusion, CRFE computes an informative set of functional categories that summarizes genome-wide expression data. With its superior performance over existing methods, CRFE harbors great promise to become a widely used functional enrichment method. Author summaryGiven a list of differentially expressed genes as input, functional enrichment methods reveal which functional categories (e.g., biological processes) were likely activated by the cell and are responsible for the differential expression. We developed a new such method, called Concise Ranked Functional Enrichment (CRFE), which addresses the limitations of current approaches by incorporating gene ranking information to compute a concise and specific set of enriched functional categories. Using four treatment-control RNA-seq datasets, we evaluate how well CRFE and the two currently most widely used methods perform in three criteria. We find that CRFE outperforms each of the alternative methods in at least one of the evaluated criteria, demonstrating its superiority. A high-level interpretation of the functional categories identified by CRFE for lung adenocarcinoma datasets highlights its usefulness for experimentalists. Overall, CRFE harnesses the power of ranked gene lists to generate a focused and non-redundant set of enriched functional categories. Our study positions CRFE as a promising method for functional enrichment analysis, with the potential to advance research in this field.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Jia, X., Phan, A., Kadelka, C.. 2023-07-02. Concise functional enrichment of ranked gene lists. https://doi.org/10.1101/2023.06.30.547164

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

spatialMET: an open and scalable framework for spatial metabolomics analysis

Mass spectrometry imaging (MSI) enables spatially resolved metabolomics in intact tissue sections, but analysis remains challenging at scale. Existing MSI workflows often require users to combine multiple software tools, while others rely on proprietary vendor software that limits interoperability and reproducibility. To address these challenges, we developed spatialMET, an open-source framework that provides an end-to-end workflow for MSI analysis. spatialMET provides a unified platform for preprocessing, spatial domain detection, and visualization. Downstream analyses include differential abundance testing, spatial autocorrelation and gradient analysis, dimensionality reduction, and correlation network analysis. Spatial domain detection uses hcdist, a C-based hierarchical clustering implementation that substantially reduces runtime and memory use relative to existing R-based approaches. spatialMET can be run through an interactive R Shiny application or as a standalone command-line workflow for larger datasets or high-performance computing environments. Applied to mouse small cell lung cancer MALDI-MSI data containing 284,673 pixels, spatialMET identified tumor-associated, stromal, and adjacent lung spatial domains that aligned with matched histology. Differential abundance analysis identified 117 m/z features that differed between tumor and stromal regions, while spatial autocorrelation analyses revealed spatially structured abundance patterns. Applying spatialMET to mouse lung adenocarcinoma data from an entire lung lobe containing 338,477 pixels further demonstrated scalability and captured spatial heterogeneity across tumor and surrounding lung tissue. In summary, spatialMET provides a scalable, open-source framework for end-to-end spatial metabolomics analysis, and it is distributed as a Docker container for reproducible deployment. Source code and installation instructions are available at https://github.com/biodatalab/spatialMET.

bioinformatics↗

Probing the transcriptome response to shivering in skeletal muscle using a multilayered bioinformatics approach

Cold acclimation holds therapeutic potential for improving metabolic health. We previously demonstrated that repeated cold-induced shivering enhances insulin sensitivity in humans. However, the molecular pathways that underlie the skeletal muscle shivering response, and how these relate to beneficial physiological effects, remain poorly understood. In this study, we combined complementary bioinformatics approaches to allow in-depth analysis of the transcriptomic response of human skeletal muscle to repeated shivering. We identified a robust transcriptional signature and show a sex-specific component in the shivering skeletal muscle response, which seemed to diminish following cold adaptation. Our findings provide mechanistic insights into cold-induced muscle adaptations, shed light on potential interesting molecular targets for further investigation, and emphasize the importance of including both sexes in future cold acclimation studies.

bioinformatics↗

An Information Geometry approach to model topological trajectories and Gene Expression Radius from UMAP geometry.

Understanding the relationship between gene expression dynamics and cellular identity remains a central challenge in single cell biology. Here, we introduce a novel computational and mathematical framework that integrates information geometry, fuzzy topology, and UMAP analysis to model gene expression landscapes derived from single cell RNA sequencing data. We formalize gene expression data as a fuzzy topological space, where interactions between expression points are governed by probabilistic distributions inspired by manifold learning approaches such as UMAP. Within this framework, we define an information geometric structure through a Fisher metric induced by these distributions, enabling the computation of geodesic trajectories that capture cellular differentiation processes. A key contribution of this work is the derivation of analytical conditions, expressed as expression radius formulas, that characterize local neighborhoods in gene expression space. These conditions allow for the identification of genes associated with stem cell states and predictions in transitional cell types in future work. Application of the proposed framework to single cell datasets reveals biologically meaningful gene sets enriched in key regulatory pathways and transcription factors, demonstrating the capacity of our approach to uncover latent structure in complex gene expression data. Our results suggest that integrating differential geometry with statistical learning theory offers a powerful paradigm for modeling genotype and phenotype relationships and cellular state transitions, with potential implications for precision medicine and systems biology.

bioinformatics↗