bioRxiv ScienceSearch

bioRxiv · 10.1101/2020.05.11.082594

YeaZ: A convolutional neural network for highly accurate, label-free segmentation of yeast microscopy images

Abstract

The processing of microscopy images constitutes a bottleneck for large-scale experiments. A critical step is the establishment of cell borders ( segmentation), which is required for a range of applications such as growth or fluorescent reporter measurements. For the model organism budding yeast (Saccharomyces cerevisiae), a number of methods for segmentation exist. However, in experiments involving multiple cell cycles, stress, or various mutants, cells crowd or exhibit irregular visible features, which necessitate frequent manual corrections. Furthermore, budding events are visually subtle but important to detect. Convolutional neural networks (CNNs) have been successfully employed for a range of image processing applications. They require large, diverse training sets. Here, we present i) the first set of publicly available, high-quality segmented yeast images (>10000 cells) including mutants, stressed cells, and time courses, ii) a corresponding U-Net-based CNN, iii) a Python-based graphical user interface (GUI) to efficiently use the system, and iv) a web application to test it (www.quantsysbio.com). A key feature is a cell-cell boundary test which avoids the need for additional input from fluorescent channels. A bipartite graph matching algorithm tracks cells in time with high reliability. Our network is highly accurate and outperforms existing methods on benchmark images recorded by others, suggesting it transfers well to other conditions. Furthermore, new buds are detected early with high reliability. We apply the system to detect differences in geometry between wild-type and cyclin mutant cells. Our results indicate that morphogenesis control occurs unexpectedly early in the cell cycle and is gradual, demonstrating how the efficient processing of large numbers of cells uncovers new biology. Our system can serve as a resource to the community, expanded continuously with new images. Furthermore, the techniques we develop here are likely to be useful for other organisms as well. The identification of cell borders ( segmentation) in microscopy images constitutes a bottleneck for large-scale experiments. For the model organism Saccharomyces cerevisiae, current segmentation methods face challenges when cells bud, crowd, or exhibit irregular features. Here, we present i) the first set of publicly available, high-quality segmented yeast images (>10000 cells) including mutants, stressed cells, and time courses, ii) a corresponding convolutional neural network (CNN), iii) a graphical user interface and a web application (www.quantsysbio.com) to efficiently employ, test, and expand the system. A key feature is a cell-cell boundary test which avoids the need for fluorescent markers. Our CNN is highly accurate, including for buds, and outperforms existing methods on benchmark images, indicating it transfers well to other conditions. To demonstrate how efficient, large-scale image processing uncovers new biology, we analyzed the geometries of {approx}2200 wild-type and cyclin mutant cells and found that morphogenesis control occurs unexpectedly early and gradually.

Source connections

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Dietler, N., Minder, M., Gligorovski, V., Economou, A. M., Joly, D. A. H. L., Sadeghi, A., Chan, C. H. M., Kozinski, M., Weigert, M., Bitbol, A.-F., Rahi, S. J.. 2020-05-12. YeaZ: A convolutional neural network for highly accurate, label-free segmentation of yeast microscopy images. https://doi.org/10.1101/2020.05.11.082594

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