PCIM: Learning pixel attributions via pixel-wise channel isolation mixing in high content imaging

IF 2.7 4区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS
SLAS Discovery Pub Date : 2025-12-01 Epub Date: 2025-11-20 DOI:10.1016/j.slasd.2025.100287
Daniel Siegismund, Mario Wieser, Stephan Heyse, Stephan Steigele
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引用次数: 0

Abstract

Deep Neural Networks (DNNs) have shown remarkable success in various computer vision tasks. However, their black-box nature often leads to difficulty in interpreting their decisions, creating an unfilled need for methods to explain the decisions, and ultimately forming a barrier to their wide acceptance especially in biomedical applications. This work introduces a novel method, Pixel-wise Channel Isolation Mixing (PCIM), to calculate pixel attribution maps, highlighting the image parts most crucial for a classification decision but without the need to extract internal network states or gradients. Unlike existing methods, PCIM treats each pixel as a distinct input channel and trains a blending layer to mix these pixels, reflecting specific classifications. This unique approach allows the generation of pixel attribution maps for each image, but agnostic to the choice of the underlying classification network. Benchmark testing on three application relevant, diverse high content Imaging datasets show state-of-the-art performance, particularly for model fidelity and localization ability in both, fluorescence and bright field High Content Imaging. PCIM contributes as a unique and effective method for creating pixel-level attribution maps from arbitrary DNNs, enabling interpretability and trust.
PCIM:在高内容成像中通过像素通道隔离混合学习像素属性。
深度神经网络(dnn)在各种计算机视觉任务中取得了显著的成功。然而,它们的黑箱性质往往导致难以解释它们的决定,对解释这些决定的方法产生了未填补的需求,并最终形成了它们被广泛接受的障碍,特别是在生物医学应用中。这项工作引入了一种新的方法,像素通道隔离混合(PCIM),用于计算像素属性图,突出显示对分类决策最关键的图像部分,但不需要提取内部网络状态或梯度。与现有的方法不同,PCIM将每个像素视为一个不同的输入通道,并训练一个混合层来混合这些像素,反映特定的分类。这种独特的方法允许为每个图像生成像素属性图,但与底层分类网络的选择无关。在三个应用相关的、不同的高内容成像数据集上的基准测试显示了最先进的性能,特别是在荧光和亮场高内容成像的模型保真度和定位能力方面。PCIM作为一种独特而有效的方法,可以从任意dnn中创建像素级属性图,从而实现可解释性和信任度。
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来源期刊
SLAS Discovery
SLAS Discovery Chemistry-Analytical Chemistry
CiteScore
7.00
自引率
3.20%
发文量
58
审稿时长
39 days
期刊介绍: Advancing Life Sciences R&D: SLAS Discovery reports how scientists develop and utilize novel technologies and/or approaches to provide and characterize chemical and biological tools to understand and treat human disease. SLAS Discovery is a peer-reviewed journal that publishes scientific reports that enable and improve target validation, evaluate current drug discovery technologies, provide novel research tools, and incorporate research approaches that enhance depth of knowledge and drug discovery success. SLAS Discovery emphasizes scientific and technical advances in target identification/validation (including chemical probes, RNA silencing, gene editing technologies); biomarker discovery; assay development; virtual, medium- or high-throughput screening (biochemical and biological, biophysical, phenotypic, toxicological, ADME); lead generation/optimization; chemical biology; and informatics (data analysis, image analysis, statistics, bio- and chemo-informatics). Review articles on target biology, new paradigms in drug discovery and advances in drug discovery technologies. SLAS Discovery is of particular interest to those involved in analytical chemistry, applied microbiology, automation, biochemistry, bioengineering, biomedical optics, biotechnology, bioinformatics, cell biology, DNA science and technology, genetics, information technology, medicinal chemistry, molecular biology, natural products chemistry, organic chemistry, pharmacology, spectroscopy, and toxicology. SLAS Discovery is a member of the Committee on Publication Ethics (COPE) and was published previously (1996-2016) as the Journal of Biomolecular Screening (JBS).
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