bioRxiv Science⌕ Search

Biology subjects

Eder, B.

Publications and source records attributed to Eder, B..

3 recordsLinked to original sources

Rectangle: robust and scalable multiscale deconvolution informed by single-cell RNA sequencing data

Bulk RNA-seq enables effective profiling of large cohorts and complex experimental designs, but current single-cell-informed deconvolution methods incompletely resolve closely related cell phenotypes, do not scale efficiently to large single-cell datasets, or fail to account for cellular content not represented in the reference. Here, we present Rectangle, an scverse Python framework for single-cell-informed deconvolution of bulk RNA-seq data. Rectangle combines multiscale deconvolution, capturing cellular composition across multiple resolution levels, with explicit modeling of unknown cellular content. In a diverse, cross-method benchmark, Rectangle achieved consistently strong performance across all evaluated metrics, demonstrating high accuracy, high resolution, low spillover, strong scalability and efficiency, and robustness to unknown cellular content. By bridging the resolution of single-cell transcriptomics with the scale and cost-efficiency of bulk RNA-seq, Rectangle enables cell-type and cell-state profiling at scale, supporting population-scale cellular biomarker discovery and tracking of cellular dynamics in settings impractical for comprehensive single-cell sequencing.

bioinformatics↗

Benchmarking second-generation methods for cell-type deconvolution of transcriptomic data

BackgroundIn silico cell-type deconvolution from bulk transcriptomics data is a powerful technique to gain insights into the cellular composition of complex tissues. While first-generation methods used precomputed expression signatures covering limited cell types and tissues, second-generation tools use single-cell RNA sequencing data to build custom signatures for deconvoluting arbitrary cell types, tissues, and organisms. This flexibility poses significant challenges in assessing their deconvolution performance. ResultsHere, we comprehensively benchmark second-generation tools, disentangling different sources of variation and bias using a diverse panel of real and simulated data. Our results reveal substantial differences in accuracy, scalability, and robustness across methods, depending on factors such as cell-type similarity, reference composition, and dataset origin. Conclusions.Our study highlights the strengths, limitations, and complementarity of state-of-the-art tools, shedding light on how different data characteristics and confounders impact deconvolution performance. We provide the scientific community with an ecosystem of tools and resources, omnideconv, simplifying the application, benchmarking, and optimization of deconvolution methods.

bioinformatics↗

Repressive gene regulation synchronizes development with cellular metabolism

Metabolic conditions affect the developmental tempo of most animal species. Consequently, developmental gene regulatory networks (GRNs) must faithfully adjust their dynamics to a variable time scale. We find evidence that layered weak repression of genes provides the necessary coupling between GRN output and cellular metabolism. Using a mathematical model that replicates such a scenario, we find that lowering metabolism corrects developmental errors that otherwise occur when different layers of repression are lost. Through mutant analysis, we show that gene expression dynamics are unaffected by loss of repressors, but only when cellular metabolism is reduced. We further show that when metabolism is lowered, formation of a variety of sensory organs in Drosophila is normal despite loss of individual repressors of transcription, mRNA stability, and protein stability. We demonstrate the universality of this phenomenon by experimentally eliminating the entire microRNA family of repressors, and find that all microRNAs are rendered unnecessary when metabolism is reduced. Thus, layered weak repression provides robustness through error frequency suppression, and may provide an evolutionary route to a shorter reproductive cycle.

developmental biology↗