bioRxiv Science⌕ Search
Home/Archive/bioRxiv

bioRxiv · 10.1101/2021.12.22.473941

Fast Medical Image Auto-segmentation for Bleeding Gastric Tissue Detection based on Deep DuS-KFCM Clustering

Liu, X. X.·Li, G.·Luo, W.·Gao, J.·Fong, S.
View original source ↗Export metadata ↓

Abstract

BackgroundDetection and classification of gastric bleeding tissues are one of the challenging tasks in endoscopy image analysis. Lesion detection plays an important role in gastric cancer (GC) diagnosis and follow-up. Manual segmentation of endoscopy images is a very time-consuming task and subject to intra- and interrater variability. Accurate GB segmentation in abdominal sequences is an essential and crucial task for surgical planning and navigation in gastric lesion ablation. However, GB segmentation in endoscope is a substantially challenging work because the intensity values of gastric blood are similar to those of adjacent structures. ObjectiveIn this paper the idea is to combine two parts: Neural Network and Fuzzy Logic--Hybrid Neuro-Fuzzy system. The objective of this manuscript is to provide an efficient way to segment the gastric bleeding lesion area. This work focuses on design and development of an automated diagnostic system using gastric bleeding cancer endoscopy images. MethodsIn this paper, a coarse-to-fine method was applied to segment gastric bleeding lesion from endoscopy images, which consists of two stages including rough segmentation and refined segmentation. The rough segmentation is based on a kernel fuzzy C-means algorithm with spatial information (SKFCM) algorithm combined with spatial gray level co-occurrence matrix (GLCM) and the refined segmentation is implemented with deeplabv3+ (backbone with resnet50) algorithm to improve the overall accuracy. ResultsExperimental results for gastric bleeding segmentation show that the method provides an accuracy of 87.9476% with specificity of 96.3343% and performs better than other related methods. onclusionsThe performance of the method was evaluated using two benchmark datasets: The GB Segmentation and the healthy datasets. Then use the gastric red spots (GRS) dataset to do the final test to verify weak bleeding symptoms. Our method achieves high accuracy in gastric bleeding lesion segmentation. The work describes an innovative way of using GLCM based textural features to extract underlying information in gastric bleeding cancer imagery. Modified deep DuS-KFCM endoscopy image segmentation method based on GLCM feature, The experimental results shown to be effective in image segmentation and has good performance of resisting noise, segmentation effect more ideal.

Explore related subjects

bioinformaticsPreprint

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Liu, X. X., Li, G., Luo, W., Gao, J., Fong, S.. 2021-12-23. Fast Medical Image Auto-segmentation for Bleeding Gastric Tissue Detection based on Deep DuS-KFCM Clustering. https://doi.org/10.1101/2021.12.22.473941

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

bioRxiv2026

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↗
bioRxiv2026

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↗
bioRxiv2026

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↗