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Koelzer, V. H.

Publications and source records attributed to Koelzer, V. H..

13 recordsLinked to original sources

Probabilistic uncertainty in virtual spatial transcriptomics from histology is largely redundant with the predicted mean

Deep learning has enabled virtual spatial transcriptomics from histology, offering a scalable approach to molecular profiling of routinely archived tissue without molecular assays. However, reliable uncertainty estimates are essential for identifying potentially inaccurate predictions, and it remains unclear whether existing methods provide useful information about prediction reliability. Here, we present a systematic benchmark of uncertainty estimation for virtual spatial transcriptomics across three cancer cohorts spanning melanoma, lung, and kidney tumors. We evaluate aleatoric and epistemic uncertainty using probabilistic likelihoods and approximate Bayesian methods alongside histology-free and training-free baselines, assessing both calibration and error informativeness. Across cohorts and methods, uncertainty is associated with prediction error, but the predicted mean largely explains this association. After accounting for the mean, uncertainty provides only weak information about larger errors. Moreover, good calibration does not imply informative uncertainty, with simple distributions fitted without histology achieving comparable calibration. We therefore distinguish calibrated from informative uncertainty and argue that uncertainty should provide information about prediction error beyond the predicted mean. This benchmark provides a framework for systematic uncertainty evaluation in virtual spatial transcriptomics. Code availability: https://github.com/ratschlab/uncertainty-vst-2026

bioinformatics↗

An RFX-driven ciliogenic cell state defines ex vivo FGFR-inhibitor sensitivity in colorectal cancer

Genomic stratification leaves most patients with colorectal cancer (CRC) without opportunities for targeted therapy. Seeking tumour state-linked drug sensitivities, we combined image-based ex vivo drug profiling with matched transcriptomics in 127 prospectively collected patient biopsies across CRC stages and molecular subtypes. Network-level integration identified a ciliogenic cell state defined by upregulation of cilia related genes with selective sensitivity to the FGFR inhibitor erdafitinib. This ciliogenic signature was associated with poor progression-free survival (hazard ratio 2.28; adjusted p=0.0098), even in early-stage colorectal cancer. Furthermore, knockdown of the transcriptional regulators RFX2 and RFX3, upstream of the ciliogenic cell state, attenuated erdafitinib sensitivity. Orthogonal bulk and single-cell analyses across normal, primary and metastatic tissues contextualised the ciliogenic programme along a transition from canonical epithelial states towards fetal and non-canonical tumour states, concomitant with Wnt-related remodelling, FGFR1/FGFR2 upregulation, and loss of intestinal epithelial identity. Together, these findings define a tumour-intrinsic ciliogenic cell state as a feature of CRC progression, revealing a patient-stratified repurposing opportunity for targeted therapy beyond the current CRC treatment paradigms.

cancer biology↗

Slide-level batch structure limits histology-guided supervision of transcriptomic foundation models

Spatial transcriptomics pairs spatially resolved gene expression with tissue morphology in the same tissue section. Transcriptomic foundation models encode such expression profiles into general-purpose representations, but these representations can retain slide- and cohort-specific variation that obscures biological signal. Here, we test whether matched H\&E histology can improve these representations as a training-time supervisory signal that is discarded at inference. Across three transcriptomic foundation models, histology-guided supervision provides no consistent aggregate improvement in cross-donor annotation transfer, despite substantially stronger transfer from histology alone. We find that gene-expression embeddings from spot-based spatial transcriptomics are low-dimensional and strongly structured by slide identity, limiting the shared gene--morphology signal available for cross-modal transfer. Guidance benefits some morphologically distinctive classes but reduces held-out gene predictivity broadly across the transcriptome. These results suggest that cross-modal supervision can reorganize information already encoded in a frozen representation but cannot recover information the representation does not retain, highlighting the importance of diagnosing slide-specific structure before applying such supervision. Code availability: https://github.com/ratschlab/vision-guided-transcriptomics-fm-2026

bioinformatics↗

Towards Cross-Sample Alignment for Multi-Modal Representation Learning in Spatial Transcriptomics

AO_SCPLOWBSTRACTC_SCPLOWThe growing number of spatial transcriptomics (ST) datasets enables comprehensive multi-modal characterization of cell types across diverse biological and clinical contexts. However, integration across patient cohorts remains challenging, as local microenvironment, patient-specific variability, and technical batch effects can dominate signals. Here, we hypothesize that combining specialized transcriptomics correction methods with deep representation learning can jointly align morphology, transcriptomics, and spatial information across multiple tissue samples. This approach benefits from recent transcriptomics and pathology foundation models, projecting cells into a shared embedding space where they cluster by cell type rather than dataset-specific conditions. Applying this framework to 18 skin melanoma, 12 human brain, and 4 lung cancer datasets, we demonstrate that it outperforms conventional batch-correction approaches by 58%, 38%, and 2-fold, respectively. Together, this framework enables efficient integration of multi-modal ST data across modalities and samples, facilitating the systematic discovery of conserved cellular programs and spatial niches while remaining robust to cohort-specific batch effects. Code availabilityhttps://github.com/ratschlab/aestetik

bioinformatics↗

RIPPLET: Mutation-Only Gene and Pathway Profiling for Precision Oncology

Clinical implementation of comprehensive genomic profiling, via whole-genome (WGS) or whole-exome sequencing (WES), is constrained by sparse mutation burdens and analytic pipelines reliant on matched transcriptomes. Currently, gene-centric analysis prevails, but overlooks the complex, multigene and pathway perturbations shaping tumor biology. We introduce RIPPLET, a DNA-only framework converting somatic variants into quantitative gene-impact scores and topology-aware pathway-perturbation profiles. By integrating tissue-specific protein-protein interaction networks with cohort-informed reweighting, RIPPLET prioritizes likely functionally relevant alterations. Applied across 33 TCGA cancer types, RIPPLET surpasses four state-of-the-art multi-omic driver-prioritization tools in recovering cancer type-specific drivers. In a cohort of metastatic cutaneous melanomas, it identifies pathway signatures that predict drug response, provide prognostic insight and distinguish immune-infiltration phenotypes without RNA data, independently validated on an in-house cohort. RIPPLET enables DNA-only inference of tumor-specific gene and pathway dysregulation, aligning with clinical sequencing workflows and offering a scalable precision-oncology strategy in transcriptome-limited settings.

bioinformatics↗

Molecularly informed analysis of histopathology images using natural language

Histopathology refers to the microscopic examination of diseased tissues and routinely guides treatment decisions for cancer and other diseases. Currently, this analysis focuses on morphological features but rarely considers gene expression information, which can add an important molecular dimension. Here, we introduce SpotWhisperer, an AI method that links histopathological images to spatial gene expression profiles and their text annotations, enabling molecularly grounded histopathology analysis through natural language. Our method outperforms pathology vision-language models on a newly curated benchmark dataset, dedicated to spatially resolved H&E annotation. Integrated into a web interface, SpotWhisperer enables interactive exploration of cell types and disease mechanisms using free-text queries with access to inferred spatial gene expression profiles. In summary, SpotWhisperer analyzes cost-effective pathology images with spatial gene expression and natural-language AI, demonstrating a path for routine integration of microscopic molecular information into histopathology.

bioinformatics↗

Generative cerebral vasculature visualization using spatialtranscriptomic data

The brain is sustained by an intricate vascular network that provides a continuous supply of nutrients and oxygen essential for its function. Understanding the structural variability and region-specific function of this neurovascular system is essential for interpreting neurological alterations in disease models. Leveraging the spatial mRNA-guided generative model Tera-MIND (simulating Tera-scale Mouse braINs using a patch-based and boundary-aware Diffusion model), we propose to predict the spatial organization of brain vasculature by the co-expression patterns of Cldn5 and Acta2 genes and their learned attention map at cell-level resolution. These findings demonstrate the capability of generative AI models trained on single-cell spatial transcriptomic data to reconstruct biologically meaningful higher-order structures. They highlight the potential of such models as in silico systems - GenAI-based simulations that generate realistic representations of biological architecture from spatial molecular data - for high-throughput exploration of vascular function and its dysregulation in neurological disorders. Taken together, our approach repurposes existing spatial transcriptomics datasets to derive new spatial insights into vascular organization, without the need for additional tissue processing. Significance StatementThe brains vascular network is complex and functionally essential. Accurate reconstruction of this network at single-cell transcriptomic resolution is key to understanding neurovascular disorders. This study applies spatial transcriptomic and histological data to generate representations of brain vasculature using Tera-MIND, providing a framework that offers a scalable approach for understanding vascular organization.

neuroscience↗

IST-editing: Infinite spatial transcriptomic editing in a generated gigapixel mouse pup

Advanced spatial transcriptomics (ST) techniques provide comprehensive insights into complex living systems across multiple scales, while simultaneously posing challenges in bioimage analysis. The spatial co-profiling of biological tissues by gigapixel whole slide images (WSI) and gene expression arrays motivates the development of innovative and efficient algorithmic approaches. Using Generative Adversarial Nets (GAN), we introduce Infinite Spatial Transcriptomic editing (IST-editing) and establish gene expression-guided editing in a generated gigapixel mouse pup. Trained with patch-wise high-plex gene expression (input) and matched image data (output), IST-editing enables the synthesis of arbitrarily large bioimages at inference, e.g., with a 106496x53248 resolution. After feeding edited gene expressions to the trained network, we model cell-, tissue- and animal-level morphological transitions in the generated mouse pup. Lastly, we discuss and evaluate editing effects on interpretable morphological features. The generated WSIs of the mouse pup and code are publicly released and accessible via https://github.com/CTPLab/IST-editing.

bioinformatics↗

In silico spatial transcriptomic editing at single-cell resolution

MotivationGenerative artificial intelligence (AI) has enabled fundamental breakthroughs in visual content creation by text-guided editing. However, the utility of such generative models remains largely understudied for processing increasingly complex bioimage data. ResultsWe propose to algorithmically edit gene expression data to drive cell-level morphological transitions using Generative Adversarial Networks (GAN) and GAN Inversion models. Leveraging cutting-edge spatial transcriptomic datasets with subcellular in-situ resolution and matched high-content imaging data, we propose an in-silico approach to quantify, model and imitate pathological processes in real-life clinical tissue samples. Availability and implementationThe code and video demo is accessible via https://github.com/CTPLab/In-silico-editing

bioinformatics↗

LEA: Latent Eigenvalue Analysis in application to high-throughput phenotypic profiling

Modeling heterogeneous disease states by data-driven methods has great potential to advance biomedical research. However, a comprehensive analysis of phenotypic heterogeneity is often challenged by the complex nature of biomedical datasets and emerging imaging methodologies. Here, we propose a novel GAN Inversion-enabled Latent Eigenvalue Analysis (GILEA) framework and apply it to phenome profiling and editing. As key use cases for fluorescence and natural imaging, we demonstrate the power of GILEA using publicly available SARS-CoV-2 datasets stained with the multiplexed fluorescence cell-painting protocol as well as real-world medical images of common skin lesions captured by dermoscopy. The quantitative results of GILEA can be biologically supported by editing latent representations and simulating dynamic phenotype transitions between physiological and pathological states. In conclusion, GILEA represents a new and broadly applicable approach to the quantitative and interpretable analysis of biomedical image data. The GILEA code and video demos are publicly available at https://github.com/CTPLab/GILEA.

bioinformatics↗

Molecular phenotyping of colorectal neoplasia shows dynamic and adaptive cancer stem cell population admixture

Intestinal homeostasis is underpinned by LGR5+ve crypt-base columnar stem cells (CBCs), but following injury, dedifferentiation results in the emergence of LGR5-ve regenerative stem cell populations (RSCs), characterised by fetal transcriptional profiles. Neoplasia hijacks regenerative signalling, so we assessed the distribution of CBCs and RSCs in mouse and human intestinal tumors. Using combined molecular-morphological analysis we demonstrate variable expression of stem cell markers across a range of lesions. The degree of CBC-RSC admixture was associated with both epithelial mutation and microenvironmental signalling disruption, and could be mapped across disease molecular subtypes. The CBC-RSC equilibrium was adaptive, with a dynamic response to acute selective pressure, and adaptability was associated with chemoresistance. We propose a fitness landscape model where individual tumors have equilibrated stem cell population distributions along a CBC-RSC phenotypic axis. Cellular plasticity is represented by position shift along this axis, and is influenced by cell-intrinsic, extrinsic and therapeutic selective pressures.

cancer biology↗

Biological misinterpretation of transcriptional signatures in tumour samples can unknowingly undermine mechanistic understanding and faithful alignment with preclinical data

Precise mechanism-based gene expression signatures (GESs) have been developed in appropriate in vitro and in vivo model systems, to identify important cancer-related signalling processes. However, some GESs originally developed to represent specific disease processes, primarily with an epithelial cell focus, are being applied to heterogeneous tumour samples where the expression of the genes in the signature may no longer be epithelial-specific. Therefore, unknowingly, even small changes in tumour stroma percentage can directly influence GESs, undermining the intended mechanistic signalling. Using colorectal cancer as an exemplar, we deployed numerous orthogonal profiling methodologies, including laser capture microdissection, flow cytometry, bulk and multiregional biopsy clinical samples, single cell RNAseq and finally spatial transcriptomics, to perform a comprehensive assessment of the potential for the most widely-used GESs to be influenced, or confounded, by stromal content in tumour tissue. To complement this work, we generated a freely-available resource, ConfoundR; https://confoundr.qub.ac.uk/, that enables users to test the extent of stromal influence on an unlimited number of the genes/signatures simultaneously across colorectal, breast, pancreatic, ovarian and prostate cancer datasets. Findings presented here demonstrate the clear potential for misinterpretation of the meaning of GESs, due to widespread stromal influences, which in-turn can undermine faithful alignment between clinical samples and preclinical data/models, particularly cell lines and organoids, or tumour models not fully recapitulating the stromal and immune microenvironment. As such, efforts to faithfully align preclinical models of disease using phenotypically-designed GESs must ensure that the signatures themselves remain representative of the same biology when applied to clinical samples.

cancer biology↗

BMP pathway antagonism by Grem1 regulates epithelial cell fate in intestinal regeneration

In the intestine, the homeostatic effect of Bone Morphogenetic Protein (BMP) on cell fate has predominantly been inferred through pathway inactivation. Here, we assessed the impact of autocrine Bmp4 expression on secretory cell fate. Ligand exposure reduced proliferation, expedited terminal differentiation, abrogated long-term secretory cell survival and prevented dedifferentiation. As stem cell plasticity is required for regenerative adaptive reprogramming, we spatiotemporally mapped and functionally explored BMPs role in epithelial restitution. Following ulceration, physiological attenuation of BMP signalling arose through upregulation of the secreted antagonist, Grem1, from topographically distinct populations of stromal cells. Concomitant expression supported functional compensation, following Grem1 deletion from tissue-resident fibroblasts. BMP pathway manipulation showed that antagonist-mediated BMP attenuation was obligatory, but functionally sub-maximal, as regeneration was impaired or enhanced by epithelial overexpression of Bmp4 or Grem1 respectively. Mechanistically, Bmp4 abrogated regenerative stem cell reprogramming, despite a convergent impact of YAP/TAZ on cell fate in remodelled wounds.

cell biology↗