Pulmonary diseases rank prominently among the principal causes of death worldwide. Curing them will require, among other things, a better understanding of the complex 3D tree-shaped structures within the pulmonary system, such as airways, arteries, and veins. Traditional approaches using high-resolution image stacks and standard CNNs on dense voxel grids face challenges in computational efficiency, limited resolution, local context, and inadequate preservation of shape topology. Our method addresses these issues by shifting from dense voxel to sparse point representation, offering better memory efficiency and global context utilization. However, the inherent sparsity in point representation can lead to a loss of crucial connectivity in tree-shaped structures. To mitigate this, we introduce graph learning on skeletonized structures, incorporating differentiable feature fusion for improved topology and long-distance context capture. Furthermore, we employ an implicit function for efficient conversion of sparse representations into dense reconstructions end-to-end. The proposed method not only delivers state-of-the-art performance in labeling accuracy, both overall and at key locations, but also enables efficient inference and the generation of closed surface shapes. Addressing data scarcity in this field, we have also curated a comprehensive dataset to validate our approach. Data and code are available at https://github.com/M3DV/pulmonary-tree-labeling.
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http://dx.doi.org/10.1016/j.media.2024.103367 | DOI Listing |
Comput Biol Med
December 2024
Khalifa University, Abu Dhabi, United Arab Emirates.
Background And Objective: Accurate extraction of retinal vascular components is vital in diagnosing and treating retinal diseases. Achieving precise segmentation of retinal blood vessels is challenging due to their complex structure and overlapping vessels with other anatomical features. Existing deep neural networks often suffer from false positives at vessel branches or missing fragile vessel patterns.
View Article and Find Full Text PDFMed Image Anal
January 2025
Computer Vision Laboratory, Swiss Federal Institute of Technology Lausanne (EPFL), Lausanne 1015, Switzerland.
Pulmonary diseases rank prominently among the principal causes of death worldwide. Curing them will require, among other things, a better understanding of the complex 3D tree-shaped structures within the pulmonary system, such as airways, arteries, and veins. Traditional approaches using high-resolution image stacks and standard CNNs on dense voxel grids face challenges in computational efficiency, limited resolution, local context, and inadequate preservation of shape topology.
View Article and Find Full Text PDFRSC Adv
August 2024
Cellulose and Paper Department, National Research Centre 33 El Bohouth Str., PO 12622 Dokki Giza Egypt +201005888560.
Methods Mol Biol
July 2024
Turku Bioscience Centre, University of Turku and Åbo Akademi University, Turku, Finland.
Single-cell transcriptomics allows unbiased characterization of cell heterogeneity in a sample by profiling gene expression at single-cell level. These profiles capture snapshots of transient or steady states in dynamic processes, such as cell cycle, activation, or differentiation, which can be computationally ordered into a "flip-book" of cell development using trajectory inference methods. However, prediction of more complex topology structures, such as multifurcations or trees, remains challenging.
View Article and Find Full Text PDFIEEE J Biomed Health Inform
September 2024
Delineating 3D blood vessels of various anatomical structures is essential for clinical diagnosis and treatment, however, is challenging due to complex structure variations and varied imaging conditions. Although recent supervised deep learning models have demonstrated their superior capacity in automatic 3D vessel segmentation, the reliance on expensive 3D manual annotations and limited capacity for annotation reuse among different vascular structures hinder their clinical applications. To avoid the repetitive and costly annotating process for each vascular structure and make full use of existing annotations, this paper proposes a novel 3D shape-guided local discrimination (3D-SLD) model for 3D vascular segmentation under limited guidance from public 2D vessel annotations.
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