Whole slide imaging (WSI) has transformed diagnostic medicine, particularly in the field of cancer diagnosis and treatment. The use of deep learning algorithms for predicting WSIs has opened up new avenues for advanced medical diagnostics. Additionally, stain normalization can reduce the color and intensity variations present in WSI from different hospitals. As a result, deep learning classification accuracy improves. However, WSI reading and color normalization are still largely performed by using CPUs, leading to sub-optimal performance. We proposed a High-Performance Heterogeneous Computing Toolkit for Tissue Image (HCTTI) that integrates multiple computer system-level optimizations and encompasses WSI reading, tile normalization, and tile saving. We explored the potential advantages and limitations of different WSI readers and color normalization techniques in WSI analysis and the performance of different tile serialization formats for saving tiles. We found that HCTTI is 7 faster than OpenSlide for reading WSIs, GPU implementation of the Macenko normalization algorithm is 9 faster than TIAToolbox implementation, and HDF5 is faster than png and Zarr for storing normalized images in both writing (13 acceleration compared to png) and reading (2 acceleration compared to png), Specifically, HDF5 provides superior performance in handling large, complex datasets due to its efficient chunking and compression capabilities, as well as its broad support for hierarchical data management, making it very suitable for workloads like deep learning training I/O pattern that involves randomly reading large amount of small files in each training epoch. We also achieved linear acceleration in our multi-node distributed GPU implementation. To our knowledge, HCTTI is the first comprehensive toolkit that comprises distributed WSI reading, normalization, and serialization. It is 13 speedup compared to TIAToolbox implementation for normalizing a single WSI. Our findings could help pave the way for more effective and efficient deep learning-based approaches to WSI analysis, with the potential to transform medical diagnosis and treatment for a wide range of conditions. The source code of HCTTI is available at https://github.com/wangbo00129/HCTTI .
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Comput Med Imaging Graph
January 2025
CAS Key Laboratory of Molecular Imaging, Institute of Automation, Chinese Academy of Sciences, Beijing 100190, China; School of Artificial Intelligence, University of Chinese Academy of Sciences, Beijing 100049, China; National Key Laboratory of Kidney Diseases, Beijing 100853, China. Electronic address:
In clinical optical molecular imaging, the need for real-time high frame rates and low excitation doses to ensure patient safety inherently increases susceptibility to detection noise. Faced with the challenge of image degradation caused by severe noise, image denoising is essential for mitigating the trade-off between acquisition cost and image quality. However, prevailing deep learning methods exhibit uncontrollable and suboptimal performance with limited interpretability, primarily due to neglecting underlying physical model and frequency information.
View Article and Find Full Text PDFJ Neurosurg
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1Department of Neurosurgery, St. Olav's University Hospital, Trondheim, Norway.
Objective: The extent of resection (EOR) and postoperative residual tumor (RT) volume are prognostic factors in glioblastoma. Calculations of EOR and RT rely on accurate tumor segmentations. Raidionics is an open-access software that enables automatic segmentation of preoperative and early postoperative glioblastoma using pretrained deep learning models.
View Article and Find Full Text PDFJ Chem Inf Model
January 2025
Department of Medicinal Chemistry, School of Pharmacy, Fudan University, 826 Zhangheng Road, Shanghai 201203, People's Republic of China.
In recent decades, covalent inhibitors have emerged as a promising strategy for therapeutic development, leveraging their unique mechanism of forming covalent bonds with target proteins. This approach offers advantages such as prolonged drug efficacy, precise targeting, and the potential to overcome resistance. However, the inherent reactivity of covalent compounds presents significant challenges, leading to off-target effects and toxicities.
View Article and Find Full Text PDFPLoS Comput Biol
January 2025
Department of Biomedical Informatics, University of Colorado Anschutz School of Medicine, Aurora, Colorado, United States of America.
While single-cell experiments provide deep cellular resolution within a single sample, some single-cell experiments are inherently more challenging than bulk experiments due to dissociation difficulties, cost, or limited tissue availability. This creates a situation where we have deep cellular profiles of one sample or condition, and bulk profiles across multiple samples and conditions. To bridge this gap, we propose BuDDI (BUlk Deconvolution with Domain Invariance).
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