bioRxiv Science⌕ Search

Biology subjects

Lehtonen, O.

Publications and source records attributed to Lehtonen, O..

3 recordsLinked to original sources

Histolytics: A Panoptic Spatial Analysis Framework for Interpretable Histopathology

Quantifying spatial organization in hematoxylin and eosin (H&E)-stained whole-slide images (WSIs) is essential for uncovering tissue-level patterns relevant to pathology. We present Histolytics, an open-source, scalable Python framework for interpretable, WSI-scale histopathological analysis. Histolytics integrates panoptic segmentation with spatial querying, morphological profiling, and graph-based analytics to enable high-resolution, quantitative characterization of nuclei, tissue compartments, and the extracellular matrix (ECM). Designed to align with diagnostic reasoning, Histolytics supports segmentation with state-of-the-art deep learning models and provides modular tools for extracting biologically grounded features across entire WSIs. By leveraging spatially contextualized measurements at cellular and tissue levels, Histolytics addresses a critical gap in explainable computational pathology, offering an interpretable alternative or complement to black-box predictive models. The framework is compatible with the broader Python data science ecosystem and includes extensive documentation and pretrained models to promote widespread adoption.

bioinformatics↗

Multi-modal characterization of transcriptional programs that drive metastatic cascades to solid sites and ascites in ovarian cancer

Ovarian high-grade serous carcinoma (HGSC) is characterized by extensive intra-peritoneal dissemination and tumor heterogeneity. In the metastatic cascade, tumors utilize several transcriptional programs to translocate and survive in distant tissues. Here, we analyzed multi-modal, real-world data from 350 tumor samples across 160 patients with HGSC to identify transcriptional programs that drive intra-peritoneal metastasis and heterogeneity. We identified nine transcriptional programs, including those regulating epithelial-mesenchymal transition and immune modulation and cytoskeletal reorganization, which shape distinct metastatic trajectories to solid and ascitic environments and are associated to treatment response. Our results reveal pronounced intra-patient transcriptional heterogeneity, which in some cases surpassed inter-patient heterogeneity, highlighting the importance of multi-site sampling for accurate prognostication and combinatorial treatments in HGSC. Our extensive characterization offers novel insights into intra-peritoneal metastasis with significant prognostic implications, reveals histomorphological biomarkers for patient stratification and paves the way for innovative therapeutic strategies aimed at impairing cancer cell adaptability and limiting metastasis.

cancer biology↗

Agile workflow for interactive analysis of mass cytometry data

MotivationSingle-cell proteomics technologies, such as mass cytometry, have enabled characterization of cell-to-cell variation and cell populations at a single cell resolution. These large amounts of data, however, require dedicated, interactive tools for translating the data into knowledge. ResultsWe present a comprehensive, interactive method called Cyto to streamline analysis of large-scale cytometry data. Cyto is a workflow-based open-source solution that automatizes the use of of state-of-the-art single-cell analysis methods with interactive visualization. We show the utility of Cyto by applying it to mass cytometry data from peripheral blood and high-grade serous ovarian cancer (HGSOC) samples. Our results show that Cyto is able to reliably capture the immune cell sub-populations from peripheral blood as well as cellular compositions of unique immune- and cancer cell subpopulations in HGSOC tumor and ascites samples. AvailabilityThe method is available as a Docker container at https://hub.docker.com/r/anduril/cyto and the user guide and source code are available at https://bitbucket.org/anduril-dev/cyto Contactsampsa.hautaniemi@helsinki.fi Supplementary informationSupplementary material is available and FCS files are hosted at flowrepository.org/id/FR-FCM-Z2LW

bioinformatics↗