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Image segmentation models trained only with image-level labels have become increasingly popular as they require significantly less annotation effort than models trained with scribble, bounding box or pixel-wise annotations. While methods utilizing image-level labels achieve promising performance for the segmentation of larger-scale objects, they perform less well for the fine structures frequently encountered in biological images. In order to address this performance gap, we propose a deep network architecture based on two key principles, Global Weighted Pooling (GWP) and segmentation refinement by low-level image cues, that, together, make segmentation of fine structures possible. We apply our segmentation method to image datasets containing such fine structures, nematodes (worms + eggs) and nematode cysts immersed in organic debris objects, which is an application scenario encountered in automated soil sample screening. Supervised only with image-level labels, our approach achieves Dice coefficients of 79.72% and 58.51 % for nematode and nematode cyst segmentation, respectively.
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http://dx.doi.org/10.1109/EMBC48229.2022.9871517 | DOI Listing |
J Org Chem
September 2025
State Key Laboratory of Fine Chemicals, Frontier Science Center for Smart Materials, School of Chemical Engineering, Dalian University of Technology, Dalian 116024, China.
The first dearomative allylation of -(trialkylsilyl) benzyl chlorides with allyltributylstannane via RSi-Pd-π-benzyl intermediates is described. The reactions proceeded smoothly in the presence of a specific P,N hemilabile ligand to generate vinylsilanes bearing an allyl group in satisfactory to good yields. Systematic evaluation of phosphine ligands identified ESPmin and % Vbur (min) as key parameters correlating ligand structure with catalytic activity.
View Article and Find Full Text PDFInorg Chem
September 2025
Pacific Northwest National Laboratory, Richland, Washington 99352, United States.
The solvation structure of an Np ion in an aqueous, noncomplexing and nonoxidizing environment of trifluoromethanesulfonic (triflic) acid was investigated with X-ray absorption spectroscopy (XAS) combined with ab initio molecular dynamics (AIMD) and time-dependent density functional theory (TDDFT) calculations. Np L-edge X-ray absorption near-edge structure (XANES) and extended X-ray absorption fine structure (EXAFS) data were collected for Np in 1, 3, and 7 M triflic acid using a laboratory-scale spectrometer and separately at a synchrotron facility, producing data sets in excellent agreement. TDDFT calculations revealed a weak pre-edge feature not previously reported for Np L-edge XANES.
View Article and Find Full Text PDFPLoS One
September 2025
School of Mechanical and Automotive Engineering, Qingdao University of Technology, Qingdao, Shandong, China.
Drug-target interaction (DTI) prediction is essential for the development of novel drugs and the repurposing of existing ones. However, when the features of drug and target are applied to biological networks, there is a lack of capturing the relational features of drug-target interactions. And the corresponding multimodal models mainly depend on shallow fusion strategies, which results in suboptimal performance when trying to capture complex interaction relationships.
View Article and Find Full Text PDFIEEE Trans Med Imaging
September 2025
Computed Tomography (CT) to Cone-Beam Computed Tomography (CBCT) image registration is crucial for image-guided radiotherapy and surgical procedures. However, achieving accurate CT-CBCT registration remains challenging due to various factors such as inconsistent intensities, low contrast resolution and imaging artifacts. In this study, we propose a Context-Aware Semantics-driven Hierarchical Network (referred to as CASHNet), which hierarchically integrates context-aware semantics-encoded features into a coarse-to-fine registration scheme, to explicitly enhance semantic structural perception during progressive alignment.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
September 2025
Department of Biological Sciences and Bioengineering, Indian Institute of Technology, Kanpur 208016, India.
Agonist-induced interaction of G protein-coupled receptors (GPCRs) with β-arrestins (βarrs) is a critical mechanism that regulates the spatiotemporal pattern of receptor localization and signaling. While the underlying mechanism governing GPCR-βarr interaction is primarily conserved and involves receptor activation and phosphorylation, there are several examples of receptor-specific fine-tuning of βarr-mediated functional outcomes. Considering the key contribution of conformational plasticity of βarrs in driving receptor-specific functional responses, it is important to develop novel sensors capable of reporting distinct βarr conformations in cellular context.
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