The wide prevalence of staining variations in digital pathology presents a significant obstacle, often undermining the effectiveness of diagnosis and analysis. The current strategies to counteract this issue primarily revolve around Stain Normalization (SN) and Stain Augmentation (SA). Nonetheless, these methodologies come with inherent limitations. They struggle to adapt to the vast array of staining styles, tend to presuppose linear associations between color spaces, and often lead to unrealistic color transformations. In response to these challenges, we introduce RandStainNA++, a novel method seamlessly integrating SN and SA. This method exploits the versatility of random SN and SA within randomly selected color spaces, effectively managing variations for the foreground and background independently. By refining the transformations of staining styles for the foreground and background within a realistic scope, this strategy promotes the generation of more practical staining transformations during the training phase. Further enhancing our approach, we propose a unique self-distillation method. This technique incorporates prior knowledge of stain variation, substantially augmenting the generalization capability of the network. The striking results yield that, compared to conventional classification models, our method boosts performance by a significant margin of 16-25%. Furthermore, when juxtaposed with baseline segmentation models, the Dice score registers an increase of 0.06.
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Sci Rep
January 2025
Department of Electrical Engineering and Computer Science, University of Tennessee, Knoxville, TN, 37996, USA.
This paper presents an in-pixel contrast enhancement circuit that performs image processing directly within the pixel circuit. The circuit leverages HyperFET, a hybrid device combining a MOSFET and a phase transition material (PTM), to enhance performance. It can be tuned for different modes of operation.
View Article and Find Full Text PDFJ Neurosci
January 2025
Oregon Hearing Research Center, Oregon Health and Science University, Portland, OR 97239, USA
In everyday hearing, listeners face the challenge of understanding behaviorally relevant foreground stimuli (speech, vocalizations) in complex backgrounds (environmental, mechanical noise). Prior studies have shown that high-order areas of human auditory cortex (AC) pre-attentively form an enhanced representation of foreground stimuli in the presence of background noise. This enhancement requires identifying and grouping the features that comprise the background so they can be removed from the foreground representation.
View Article and Find Full Text PDFMed Biol Eng Comput
January 2025
School of Software, Jiangxi Normal University, Nanchang, 330022, China.
Source-free domain adaptation (SFDA) has become crucial in medical image analysis, enabling the adaptation of source models across diverse datasets without labeled target domain images. Self-training, a popular SFDA approach, iteratively refines self-generated pseudo-labels using unlabeled target domain data to adapt a pre-trained model from the source domain. However, it often faces model instability due to incorrect pseudo-label accumulation and foreground-background class imbalance.
View Article and Find Full Text PDFJ Low Temp Phys
November 2024
Princeton University, Princeton, NJ USA.
The Simons Observatory (SO) is a cosmic microwave background (CMB) experiment located in the Atacama Desert in Chile that will make precise temperature and polarization measurements over six spectral bands ranging from 27 to 285 GHz. Three small aperture telescopes (SATs) and one large aperture telescope (LAT) will house 60,000 detectors and cover angular scales between one arcminute and tens of degrees. We present the performance of the dichroic, low-frequency (LF) lenslet-coupled sinuous antenna transition-edge sensor (TES) bolometer arrays with bands centered at 27 and 39 GHz.
View Article and Find Full Text PDFBioData Min
January 2025
The Department of Computational Biomedicine, Cedars-Sinai Medical Center, Los Angeles, CA, 90069, USA.
Background: With recent advances in single cell technology, high-throughput methods provide unique insight into disease mechanisms and more importantly, cell type origin. Here, we used multi-omics data to understand how genetic variants from genome-wide association studies influence development of disease. We show in principle how to use genetic algorithms with normal, matching pairs of single-nucleus RNA- and ATAC-seq, genome annotations, and protein-protein interaction data to describe the genes and cell types collectively and their contribution to increased risk.
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