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2021 IEEE 18th International Symposium on Biomedical Imaging (ISBI)最新文献

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Deep Learning For Light Field Microscopy Using Physics-Based Models 使用基于物理模型的光场显微镜的深度学习
Pub Date : 2021-04-13 DOI: 10.1109/ISBI48211.2021.9434004
Herman Verinaz-Jadan, P. Song, Carmel L. Howe, Peter Quicke, Amanda J. Foust, P. Dragotti
Light Field Microscopy (LFM) is an imaging technique that captures 3D spatial information in a single 2D image. LFM is attractive because of its relatively simple implementation and fast acquisition rate. However, classic 3D reconstruction typically suffers from high computational cost, low lateral resolution, and reconstruction artifacts. In this work, we propose a new physics-based learning approach to improve the performance of the reconstruction under realistic conditions, these being lack of training data, background noise, and high data dimensionality. First, we propose a novel description of the system using a linear convolutional neural network. This description is complemented by a method that compacts the number of views of the acquired light field. Then, this model is used to solve the inverse problem under two scenarios. If labelled data is available, we train an end-to-end network that uses the Learned Iterative Shrinkage and Thresholding Algorithm (LISTA). If no labelled data is available, we propose an unsupervised technique that uses only unlabelled data to train LISTA by making use of Wasserstein Generative Adversarial Networks (WGANs). We experimentally show that our approach performs better than classic strategies in terms of artifact reduction and image quality.
光场显微镜(LFM)是一种成像技术,可以在单个2D图像中捕获3D空间信息。LFM以其相对简单的实现和快速的获取速度而具有吸引力。然而,经典的3D重建通常存在计算成本高、横向分辨率低和重建伪影等问题。在这项工作中,我们提出了一种新的基于物理的学习方法来提高现实条件下的重建性能,这些条件缺乏训练数据、背景噪声和高数据维数。首先,我们提出了一种新的描述系统使用线性卷积神经网络。这种描述由一种压缩所获得光场的视图数量的方法加以补充。然后,利用该模型求解了两种情况下的逆问题。如果有标记数据可用,我们训练一个端到端网络,使用学习迭代收缩和阈值算法(LISTA)。如果没有可用的标记数据,我们提出一种无监督技术,该技术仅使用未标记的数据来训练LISTA,利用Wasserstein生成对抗网络(WGANs)。实验表明,我们的方法在伪影减少和图像质量方面优于经典策略。
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引用次数: 5
Two-Stage Multi-Scale Mass Segmentation From Full Mammograms 全乳房x光片的两阶段多尺度质量分割
Pub Date : 2021-04-13 DOI: 10.1109/ISBI48211.2021.9433946
Yutong Yan, Pierre-Henri Conze, G. Quellec, M. Lamard, B. Cochener, G. Coatrieux
Manually segmenting masses from native mammograms is a very time-consuming and error-prone task. Therefore, an integrated computer-aided diagnosis (CAD) system is required to assist radiologists for automatic and precise breast mass delineation. In this work, we present a two-stage multi-scale pipeline that provides accurate mass delineations from high-resolution full mammograms. First, we propose an extended deep detector integrating a multi-scale fusion strategy for automated mass localization. Second, a convolutional encoder-decoder network using nested and dense skip connections is used to fine-delineate candidate masses. Experiments on public DDSM-CBIS and INbreast datasets reveals strong robustness against the diversity of size, shape and appearance of masses, with an average Dice of 80.44% on INbreast. This shows promising accuracy as an automated full-image mass segmentation system, towards better interaction-free CAD.
从乳房x光片中手动分割肿块是一项非常耗时且容易出错的任务。因此,需要一个集成的计算机辅助诊断(CAD)系统来协助放射科医生自动准确地描绘乳房肿块。在这项工作中,我们提出了一个两阶段的多尺度管道,从高分辨率的全乳房x线照片中提供准确的质量描绘。首先,我们提出了一种集成多尺度融合策略的扩展深度探测器,用于自动质量定位。其次,使用嵌套和密集跳跃连接的卷积编码器-解码器网络来精细描绘候选质量。在公开的dddsm - cbis和INbreast数据集上的实验表明,该方法对质量大小、形状和外观的多样性具有较强的鲁棒性,在INbreast上的平均Dice为80.44%。这显示了作为一个自动化的全图像质量分割系统的准确性,朝着更好的无交互CAD方向发展。
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引用次数: 2
Characterizing The Uncertainty Of Label Noise In Systematic Ultrasound-Guided Prostate Biopsy 超声引导前列腺活检中标记噪声不确定性的表征
Pub Date : 2021-04-13 DOI: 10.1109/ISBI48211.2021.9433765
Golara Javadi, S. Samadi, Sharareh Bayat, Samira Sojoudi, Antonio Hurtado, Silvia D. Chang, Peter C. Black, P. Mousavi, P. Abolmaesumi
Ultrasound imaging is a common tool used in prostate biopsy. The challenges associated with using a systematic and nontargeted approach are the high rate of false negatives and not being patient specific. Intraprostatic pathology information of individuals is not available during the biopsy procedure. Even after histopathology analysis of the biopsy cores, the report only represents a statistical distribution of cancer within the core. Labeling the data based on these noisy labels results in challenges for network training, where networks inevitably overfit to noisy data. To overcome this problem, we argue that it is critical to build a clean dataset. In this paper, we address the challenges associated with using statistical labels and alleviate this issue by taking advantage of confident learning to estimate uncertainty in the data label. Next, we find the label error, clean the labels, and evaluate the clean data by comparing it using a metric based on the involvement of cancer in core.
超声成像是前列腺活检中常用的工具。使用系统和非针对性方法的挑战是假阴性率高,并且不针对患者。在活检过程中,个体的前列腺内病理信息是不可用的。即使在对活检芯进行组织病理学分析后,该报告也仅代表了芯内癌症的统计分布。基于这些噪声标签对数据进行标记会给网络训练带来挑战,网络不可避免地会过度拟合噪声数据。为了克服这个问题,我们认为建立一个干净的数据集是至关重要的。在本文中,我们解决了与使用统计标签相关的挑战,并通过利用自信学习来估计数据标签中的不确定性来缓解这一问题。接下来,我们找到标签错误,清理标签,并通过使用基于核心癌症参与的度量来比较干净的数据。
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引用次数: 3
Enhancing HARDI Reconstruction from Undersampled Data Via Multi-Context and Feature Inter-Dependency GAN 基于多上下文和特征互依赖GAN的欠采样数据HARDI重构
Pub Date : 2021-04-13 DOI: 10.1109/ISBI48211.2021.9434162
Ranjeet Ranjan Jha, Hritik Gupta, S. Pathak, W. Schneider, B. V. R. Kumar, A. Bhavsar, A. Nigam
In addition to the more traditional diffusion tensor imaging (DTI), over time, reconstruction techniques like HARDI have been proposed, which have a comparatively higher scanning time due to increased measurements, but are significantly better in the estimation of fiber structures. In order to make HARDI-based analysis faster, we propose an approach to reconstruct more HARDI volumes in q-space. The proposed GAN-based architecture leverages several modules, including a multi-context module, feature inter-dependencies module along-with numerous losses such as L1, adversarial, and total variation loss, to learn the transformation. The method is backed by some encouraging quantitative and visual results.
除了更传统的扩散张量成像(DTI),随着时间的推移,已经提出了像HARDI这样的重建技术,由于测量量的增加,扫描时间相对较长,但在估计纤维结构方面明显更好。为了使基于HARDI的分析更快,我们提出了一种在q空间中重构更多HARDI体积的方法。提出的基于gan的体系结构利用多个模块,包括多上下文模块、特征相互依赖模块以及大量损失(如L1、对抗性和总变异损失)来学习转换。该方法得到了一些令人鼓舞的定量和可视化结果的支持。
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引用次数: 7
Towards Diffuse Beamforming For Specular Reflectors: A Pixel-Level Reflection Tuned Apodization Scheme For Ultrasound Imaging 针对镜面反射器的漫射波束形成:一种用于超声成像的像素级反射调谐apozation方案
Pub Date : 2021-04-13 DOI: 10.1109/ISBI48211.2021.9433990
Gayathri Malamal, Mahesh Raveendranatha Panicker
In the case of typical beamforming in ultrasound imaging, apodization schemes assume a geometric delay driven diffuse reflection model and are not robust for specular reflections. Conversely, the beamforming schemes exclusive to emphasizing specularity suppress the diffuse reflections and speckles. This results in separate beamforming modes for normal tissue scanning and specular reflectors like needles. However, most tissue reflections compose of both diffuse and specular components and a synergistic approach is important. Towards this, a novel approach called reflection tuned apodization (RTA) using coherent plane-wave compounding is proposed, where the apodization window is aligned appropriately by analyzing the reflections from the transmitted plane wave angles for each pixel. A reflection similarity measure is estimated from the plane wave angles to differentiate and characterize the tissue reflections. The beamforming results with the proposed RTA on experimental data show a remarkable improvement in the visibility of specular regions without the suppression of diffuse reflections and speckles compared to the conventional apodization approach.
在超声成像中典型波束形成的情况下,apodization方案采用几何延迟驱动的漫反射模型,对镜面反射不具有鲁棒性。相反,只强调镜面的波束形成方案抑制了漫反射和散斑。这就产生了用于正常组织扫描和针状反射器的独立波束形成模式。然而,大多数组织反射由漫反射和镜面反射组成,协同方法很重要。为此,提出了一种利用相干平面波复合的反射调谐apodiation (RTA)新方法,该方法通过分析每个像素的透射平面波角度的反射来调整apodiation窗口。从平面波角度估计反射相似度量,以区分和表征组织反射。实验数据表明,与传统的波束形成方法相比,该方法在不抑制漫反射和散斑的情况下显著提高了镜面区域的可见性。
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引用次数: 5
Ultrasound-Based Tracking Of Partially In-Plane, Curved Needles 部分平面内弯曲针的超声跟踪
Pub Date : 2021-04-13 DOI: 10.1109/ISBI48211.2021.9433804
Wanwen Chen, Kathan Nilesh Mehta, Bhumi Dinesh Bhanushali, J. Galeotti
We present a novel algorithm for needle tracking in ultrasound-guided needle insertion. Most previous research assumes that in ultrasound images the needle is a straight and bright line, but needles can bend due to the interaction with heterogeneous tissue. We utilize a novel weighted RANSAC curve fitting method combined with probabilistic Hough transform to track the curved needle robustly, and the algorithm can additionally utilize external tracking information, such as robotic kinematics, to further improve the tracking accuracy. We compared against classical tracking algorithms and a U-Net model, testing over different needle curvature and tissues. Our proposed algorithm achieves higher accuracy in tip location, shaft fitting, and tip angle. In-vivo porcine experiments with naturally bending short needles also show our method better tracked the tip location.
我们提出了一种新的超声引导下针头跟踪算法。大多数先前的研究假设,在超声图像中,针是一条笔直而明亮的线,但由于与异质组织的相互作用,针可能会弯曲。采用一种新的加权RANSAC曲线拟合方法结合概率霍夫变换对曲线针进行鲁棒跟踪,并利用机器人运动学等外部跟踪信息进一步提高跟踪精度。我们比较了经典的跟踪算法和U-Net模型,在不同的针曲率和组织上进行了测试。该算法在叶尖位置、轴配合和叶尖角度方面具有较高的精度。猪体内自然弯曲短针实验也表明,该方法能更好地追踪针尖位置。
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引用次数: 0
Geometric Deep Learning on Anatomical Meshes for the Prediction of Alzheimer’s Disease 基于解剖网格的几何深度学习预测阿尔茨海默病
Pub Date : 2021-04-13 DOI: 10.1109/ISBI48211.2021.9433948
Ignacio Sarasua, Jonwong Lee, C. Wachinger
Geometric deep learning can find representations that are optimal for a given task and therefore improve the performance over pre-defined representations. While current work has mainly focused on point representations, meshes also contain connectivity information and are therefore a more comprehensive characterization of the underlying anatomical surface. In this work, we evaluate four recent geometric deep learning approaches that operate on mesh representations. These approaches can be grouped into template-free and template-based approaches, where the template-based methods need a more elaborate pre-processing step with the definition of a common reference template and correspondences. We compare the different networks for the prediction of Alzheimer’s disease based on the meshes of the hippocampus. Our results show advantages for template-based methods in terms of accuracy, number of learnable parameters, and training speed. While the template creation may be limiting for some applications, neuroimaging has a long history of building templates with automated tools readily available. Overall, working with meshes is more involved than working with simplistic point clouds, but they also offer new avenues for designing geometric deep learning architectures.
几何深度学习可以找到对给定任务最优的表示,从而比预定义的表示提高性能。虽然目前的工作主要集中在点表示上,但网格也包含连接信息,因此是对底层解剖表面的更全面的表征。在这项工作中,我们评估了最近在网格表示上操作的四种几何深度学习方法。这些方法可以分为无模板方法和基于模板的方法,其中基于模板的方法需要更精细的预处理步骤,并定义公共引用模板和通信。我们比较了基于海马体网预测阿尔茨海默病的不同网络。我们的结果显示了基于模板的方法在准确性、可学习参数的数量和训练速度方面的优势。虽然模板的创建可能对某些应用程序有限制,但神经成像在使用现成的自动化工具构建模板方面有着悠久的历史。总的来说,使用网格比使用简单的点云更复杂,但它们也为设计几何深度学习架构提供了新的途径。
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引用次数: 8
Multi-Label Classification Based On Subcellular Region-Guided Feature Description For Protein Localisation 基于亚细胞区域导向特征描述的蛋白质定位多标签分类
Pub Date : 2021-04-13 DOI: 10.1109/ISBI48211.2021.9434145
Priyanka S. Rana, E. Meijering, A. Sowmya, Yang Song
In this paper, we present a multi-label classification pipeline and a novel feature descriptor for the protein subcellular localisation. The challenge here is the development of a computational model that can classify multi-site proteins on a highly imbalanced dataset with a long-tail distribution and multi-label images. To address this challenge, we design a Location-Sorted Random Projections feature descriptor to represent image intensity and gradient of the protein of interest in reference to the correlated cellular region. Multilabel Synthetic Minority Over-sampling Technique is optimised to generate synthetic features with labels to handle class imbalance. Our method achieves the state-of-the-art performance on a large-scale public dataset and demonstrates excellent performance for the minority classes.
在本文中,我们提出了一种多标签分类管道和一种新的蛋白质亚细胞定位特征描述符。这里的挑战是开发一种计算模型,该模型可以对具有长尾分布和多标签图像的高度不平衡数据集上的多位点蛋白质进行分类。为了解决这一挑战,我们设计了一个位置排序随机投影特征描述符来表示相关细胞区域感兴趣的蛋白质的图像强度和梯度。优化了多标签合成少数派过采样技术,生成带有标签的合成特征,以解决类不平衡问题。我们的方法在大规模公共数据集上实现了最先进的性能,并在少数类上展示了出色的性能。
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引用次数: 4
Low-Dose Dual KVP Switching Using A Static Coded Aperture 使用静态编码孔径的低剂量双KVP开关
Pub Date : 2021-04-13 DOI: 10.1109/ISBI48211.2021.9434080
Angela P. Cuadros, Carlos M. Restrepo, P. Noel
This paper introduces a single-scan dual-energy coded aperture computed tomography system that enables material characterization at a reduced exposure level. Rapid kVp switching with a single-static block/unblock coded aperture relies on coded illumination with a plurality of X-ray spectra created by the kVp switching. Based on the tensor representation of the projection data, an algorithm to estimate the missing measurements in the tensor is proposed. This results in a full set of synthesized measurements that can be used with filtered back-projection or iterative reconstruction algorithms to accurately reconstruct the object in each energy channel. Simulation results validate the effectiveness of the proposed cost-effective solution to attain material characterization in low-dose dual-energy CT.
本文介绍了一种单扫描双能量编码孔径计算机断层扫描系统,该系统可以在降低暴露水平下进行材料表征。单静态块/无块编码孔径的快速kVp切换依赖于编码照明,由kVp切换产生多个x射线光谱。基于投影数据的张量表示,提出了一种估计张量中缺失量的算法。这就产生了一套完整的合成测量,可以使用滤波后的反投影或迭代重建算法来精确地重建每个能量通道中的目标。仿真结果验证了该方法在低剂量双能CT中实现材料表征的有效性。
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引用次数: 0
Towards a generalization of the MP2RAGE partial volume estimation model to account for B1+ inhomogeneities at 7T 对MP2RAGE部分体积估计模型的推广,以解释7T时B1+的不均匀性
Pub Date : 2021-04-13 DOI: 10.1109/ISBI48211.2021.9434089
J. Beaumont, O. Acosta, P. Raniga, G. Gambarota, J. Fripp
Brain morphometry performed with magnetic resonance (MR) imaging is affected by partial volume (PV) effects when single voxels contain the signal from two different tissues. This paper proposes a generalization of the MP2 RAGE sequence PV estimation model which accounts for transmitted magnetic field $(B1^{+})$ inhomogeneities at 7T. Our simulation experiments demonstrated that the PV estimation error of the proposed model is significantly lower than the error obtained with the same model neglecting $B1^{+}$ inhomogeneities (p<0.0001). The accuracy and precision of the $B1^{+}$ model (acc=92.0%, prec=89.6%) was significantly increased compared to the non $B1^{+}$ model (acc=69.8%, prec=65.4%). This highlights the importance of accounting for $B1^{+}$ inhomogeneities when computing PV on MP2RAGE data, which would otherwise limit the accuracy of brain morphometry at 7T.
当单个体素包含来自两个不同组织的信号时,用磁共振(MR)成像进行的脑形态测量受到部分体积(PV)效应的影响。本文提出了考虑7T发射磁场$(B1^{+})$不均匀性的MP2 RAGE序列PV估计模型的推广。我们的仿真实验表明,该模型的PV估计误差显著低于忽略$B1^{+}$不均匀性的相同模型所获得的误差(p<0.0001)。与非$B1^{+}$模型(acc=69.8%, prec=65.4%)相比,$B1^{+}$模型的准确度和精密度(acc=92.0%, prec=89.6%)显著提高。这突出了在MP2RAGE数据上计算PV时考虑$B1^{+}$不均匀性的重要性,否则将限制7T脑形态测量的准确性。
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引用次数: 0
期刊
2021 IEEE 18th International Symposium on Biomedical Imaging (ISBI)
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