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Weis, C.-A.

Publications and source records attributed to Weis, C.-A..

3 recordsLinked to original sources

Post-operative tissue fragment puzzling using histopathological vision transformer alignment HiViTAlign

1In pathology, reconstructing adjacent tissue parts enables an overview of the macro environment of objects like tumors. Especially, malignoma are of interest to verify invasion and resection margins, as patients with positive margins face a higher mortality risk. Reassembling image fragments is widely used in other domains, but adjacent blocks in pathology are mostly analyzed separately missing global context. In this project, neighboring tissue of pig organ whole slide images (WSI) are reconstructed without a ground truth based on histological sections at the end of a complex work-up process. Histological tissue slices with artifacts, frayed or disrupted boundaries and sometimes missing pieces complicate the puzzling task. Thus, typical approaches such as direct feature comparison of tissue boundaries or estimating a tiles position based on an overview image or a known structures are not applicable. A new approach is presented using partial image registration where only parts of a fixed and a moving image are aligned for adjacency. In contrast to existing projects aligning subsequent tissue slices of the same block, WSIs from separated blocks will be reassembled for adjacency. The used three stage vision transformer extracts image features on various scales, compares neighboring tiles by shape, color and texture and predicts transformation parameters. Even though the pipeline is capable of handling rigid transformation such as rotation or reflection, only translation is currently supported due to the limited training set. Supervised training of the network can be realized using a puzzle generator creating irregular shaped fragments of masked whole slide images. The factorized trained neural network is embedded into a sophisticated histopathological vision transformer alignment (HiViTAlign) pipeline executing the following steps in roughly 10 seconds per reassembled tissue puzzle: First, extract the specimen and mask the background in each whole slide image. Second, compare tile boundaries using partial image registration. Third, calculate the adjacency by boundary proximity for each image pair. Fourth, determine a minimal spanning tree to optimize adjacency of pairwise registrations and transformations for tissue reconstruction. The python source code for HiViTAlign to start puzzling with WSIs or other objects is available at https://github.com/cpheidelberg/HiViTAlign. The generator for creating a dataset with irregular shaped tiles can be downloaded from https://github.com/cpheidelberg/ImagePuzzleGenerator. 2 Author summaryHistopathology as the microscopic analysis of tissue remains the gold standard for evaluating tumors, especially when assessing resection margins. However, the physical processing of tissue disrupts its original three dimensional structure, leaving pathologists with fragmented, two-dimensional slices that lack spatial context. This fragmentation makes it difficult to understand the full extent and orientation of tumors and to correlate pathology results with radiological imaging used in surgical planning. In this study, we present a computational pipeline for histopathological vision transformer alignment (HiViTAlign) that reassembles fragmented histological tissue sections, similar to solving a jigsaw puzzle. Using a deep learning model based on Vision Transformers, our method predicts how individual tissue fragments are spatially related and outputs transformation parameters for adjacency. While the pipeline is designed to accommodate a variety of rigid transformations (e.g., rotation and scaling), its current implementation, constrained by the limited diversity of the training dataset, focuses solely on predicting translational shifts between fragments. A custom dataset generator was developed to create realistic puzzles from whole slide images, assigning original coordinates to each fragment to enable supervised training. The full pipeline was evaluated on both synthetic datasets and real-world whole slide images, demonstrating its ability to reconstruct tissue cross-sections without requiring a reference image. This method may support more accurate spatial interpretation of pathological specimens and better integration with surgical imaging data. The open-source Python code, we developed, invites collaboration and innovation, reflecting our commitment to advancing computational pathology through technology and shared resources. Paper to be submitted to PLOS Computational Biology.

pathology↗

Unsupervised learning for labeling global glomerulosclerosis

Current deep learning models for classifying glomeruli in nephropathology are trained almost exclusively in a supervised manner, requiring expert-labeled images. Very little is known about the potential for unsupervised learning to overcome this bottleneck. To address this open question in a proof-of-concept, the project focused on the most fundamental classification task: globally sclerosed versus non-globally sclerosed glomeruli. The performance of clustering between the two classes was extensively studied across a variety of labeled datasets with diverse compositions and histological stains, and across the feature embeddings produced by 34 different pre-trained CNN models. As demonstrated by the study, clustering of globally and non-globally sclerosed glomeruli is generally highly feasible, yielding accuracies of over 95% in most datasets. Further work will be required to expand these experiments towards the clustering of additional glomerular lesion categories. We are convinced that these efforts (i) will open up opportunities for semi-automatic labeling approaches, thus alleviating the need for labor-intensive manual labeling, and (ii) illustrate that glomerular classification models can potentially be trained even in the absence of expert-derived class labels.

pathology↗

Spatial omics imaging of fresh-frozen tissue and routine FFPE histopathology on a single cancer needle core biopsy: freezing device and multimodal workflow

Complex molecular alterations underlying cancer pathophysiology are intensely studied with omics methods using bulk tissue extracts. For spatially resolved tissue diagnostics using needle biopsy cores, however, histopathological analysis using stained FFPE tissue and immuno-histochemistry (IHC) of few marker proteins is currently the main clinical focus. Today, spatial omics imaging using MSI or IRI are emerging diagnostic technologies for identification and classification of various cancer types. However, to conserve tissue-specific metabolomic states, fast, reliable and precise methods for preparation of fresh-frozen (FF) tissue sections are crucial. Such methods are often incompatible with clinical practice, since spatial metabolomics and routine histopathology of needle biopsies currently require two biopsies for FF and FFPE sampling, respectively. Therefore, we developed a device and corresponding laboratory and computational workflows for multimodal spatial omics analysis of fresh-frozen, longitudinally sectioned needle biopsies to accompany standard FFPE histopathology on the same biopsy core. As proof-of-concept, we analyzed surgical human liver cancer specimen by IRI and MSI with precise co-registration and, following FFPE processing, by sequential clinical pathology analysis on the same biopsy core. This workflow allowed spatial comparison between different spectral profiles and alterations in tissue histology, as well as direct comparison to histological diagnosis without the need of an extra biopsy. SIMPLE SUMMARYRoutine clinical approaches for cancer diagnosis demand fast, cost-efficient, and reliable methods, and their implementation within clinical settings. Currently, histopathology is the golden standard for tissue-based clinical diagnosis. Recently, spatially resolved molecular profiling techniques like mass spectrometry imaging (MSI) or infrared spectroscopy imaging (IRI) have increasingly contributed to clinical research, e.g., by differentiation of cancer subtypes using molecular fingerprints. However, adoption of the corresponding workflows in clinical routine remains challenging, especially for fresh-frozen tissue specimen. Here, we present a novel device based on 3D-printing technology, which facilitates sample preparation of needle biopsies for correlated clinical tissue analysis. It enables combination of MSI and IRI on fresh-frozen clinical samples with histopathological examination of the same needle core after formalin-fixation and paraffin-embedding (FFPE). This device and workflow can pave the way for a more profound understanding of biomolecular processes in cancer and, thus, aid more accurate diagnosis. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=180 SRC="FIGDIR/small/528125v1_ufig1.gif" ALT="Figure 1"> View larger version (55K): org.highwire.dtl.DTLVardef@1da99aborg.highwire.dtl.DTLVardef@9ee706org.highwire.dtl.DTLVardef@5153daorg.highwire.dtl.DTLVardef@1581594_HPS_FORMAT_FIGEXP M_FIG C_FIG

cancer biology↗