Search bioRxiv⌕ Search

Biology subjects

Bunten, D.

Publications and source records attributed to Bunten, D..

3 recordsLinked to original sources

Stellar quality control for single-cell image-based profiling with coSMicQC

Over the past twenty years, high-content imaging has transformed our ability to measure cell phenotypes. The need to bioinformatically process these phenotypes led to the development of a research field called image-based profiling. However, because the standard image-based profiling approach involves averaging data, single-cell quality control (QC) has been historically ignored. The conventional approach of aggregating single cells into bulk profiles conserves computational resources and reduces, but does not completely remove, the impact of low-quality single cells. As software scalability improves, researchers are increasingly turning to single-cell image-based profiling to reveal important signals of phenotypic heterogeneity. Therefore, this evolution toward single cells compels single-cell QC standards to ensure that observed morphology differences are driven by biology and not technical interference. We address these challenges with coSMicQC (Single cell Morphology Quality Control), a reproducible Python package with comprehensive tutorials that supports systematic, human-in-the-loop filtering of low-quality single cells. CoSMicQC integrates seamlessly into standard image-based profiling protocols, providing an interactive, Jupyter-compatible user interface to set thresholds and flag technical outliers. Applied to four real-world datasets, coSMicQC achieves data-quality gains comparable to labor-intensive manual annotation, at a fraction of the effort. We show how coSMicQC optimizes assay conditions, outperforms the alternative outlier detector PyOD at single-cell phenotype classification, detects mycoplasma contamination, and rescues lead compounds in a large-scale drug screen that would otherwise have been missed. Overall, coSMicQC is a reliable, scalable method for removing technical outliers, reducing noise, and strengthening image-based profiling insights.

bioinformatics↗

Scalable data harmonization for single-cell image-based profiling with CytoTable

High-content imaging (HCI) involves the automated acquisition and quantitative analysis of cell phenotypes from microscopy images. These studies often rely on screening, which can involve thousands of chemical or genetic perturbations that produce terabytes of microscopy data. To extract meaningful biological insights, this data must be processed into quantitative features through a technique known as image-based profiling. A major analytical bottleneck is curating the high-dimensional, single-cell data derived from varied image analysis tools. These datasets suffer from inconsistent schemas, inefficient file formats, and undocumented ontological relationships. These challenges reduce reproducibility and slow progress in downstream applications. To solve these issues, we introduce CytoTable1, a software package for harmonizing single-cell image-based profiling. CytoTable enables modular, portable, and cross-language data integration through a robust, reproducible, and scalable engine that harmonizes single-cell readouts from multiple image analysis tools, preparing for feature integration with software in the Cytomining ecosystem such as Pycytominer.2

bioinformatics↗

A morphology and secretome map of pyroptosis

Pyroptosis represents one type of Programmed Cell Death (PCD). It is a form of inflammatory cell death that is canonically defined by caspase-1 cleavage and Gasdermin-mediated membrane pore formation. Caspase-1 initiates the inflammatory response (through IL-1{beta} processing), and the N-terminal cleaved fragment of Gasdermin D polymerizes at the cell periphery forming pores to secrete pro-inflammatory markers. Cell morphology also changes in pyroptosis, with nuclear condensation and membrane rupture. However, recent research challenges canon, revealing a more complex secretome and morphological response in pyroptosis, including overlapping molecular characterization with other forms of cell death, such as apoptosis. Here, we take a multimodal, systems biology approach to characterize pyroptosis. We treated human Peripheral Blood Mononuclear Cells (PBMCs) with 36 different combinations of stimuli to induce pyroptosis or apoptosis. We applied both secretome profiling (nELISA) and high-content fluorescence microscopy (Cell Painting). To differentiate apoptotic, pyroptotic and control cells, we used canonical secretome markers and modified our Cell Painting assay to mark the N-terminus of Gasdermin-D. We trained hundreds of machine learning (ML) models to reveal intricate morphology signatures of pyroptosis that implicate changes across many different organelles and predict levels of many pro-inflammatory markers. Overall, our analysis provides a detailed map of pyroptosis which includes overlapping and distinct connections with apoptosis revealed through a mechanistic link between cell morphology and cell secretome.

systems biology↗