首页 > 最新文献

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

英文 中文
Federated Learning for Site Aware Chest Radiograph Screening 位置感知胸片筛查的联合学习
Pub Date : 2021-04-13 DOI: 10.1109/ISBI48211.2021.9433876
A. Chakravarty, Avik Kar, Ramanathan Sethuraman, D. Sheet
The shortage of Radiologists is inspiring the development of Deep Learning (DL) based solutions for detecting cardio, thoracic and pulmonary pathologies in Chest radiographs through multi-institutional collaborations. However, sharing the training data across multiple sites is often impossible due to privacy, ownership and technical challenges. Although Federated Learning (FL) has emerged as a solution to this, the large variations in disease prevalence and co-morbidity distributions across the sites may hinder proper training. We propose a DL architecture with a Convolutional Neural Network (CNN) followed by a Graph Neural Network (GNN) to address this issue. The CNN-GNN model is trained by modifying the Federated Averaging algorithm. The CNN weights are shared across all sites to extract robust features while separate GNN models are trained at each site to leverage the local co-morbidity dependencies for multi-label disease classification. The CheXpert dataset is partitioned across five sites to simulate the FL set up. Federated training did not show any significant drop in performance over centralized training. The site-specific GNN models also demonstrated their efficacy in modelling local disease co-occurrence statistics leading to an average area under the ROC curve of 0.79 with a 1.74% improvement.
放射科医生的短缺激发了基于深度学习(DL)的解决方案的发展,通过多机构合作,在胸部x光片中检测心脏、胸部和肺部病变。然而,由于隐私、所有权和技术挑战,跨多个站点共享培训数据通常是不可能的。尽管联邦学习(FL)已成为解决这一问题的一种方法,但各站点之间疾病患病率和共发病分布的巨大差异可能会妨碍适当的培训。我们提出了一个卷积神经网络(CNN)和图神经网络(GNN)的深度学习架构来解决这个问题。通过修改联邦平均算法训练CNN-GNN模型。CNN权重在所有站点之间共享,以提取鲁棒特征,同时在每个站点训练单独的GNN模型,以利用局部共发病依赖关系进行多标签疾病分类。CheXpert数据集跨五个站点进行分区,以模拟FL设置。与集中式训练相比,联合训练没有显示出任何显著的性能下降。特异位点GNN模型在模拟局部疾病共发生统计方面也显示出其有效性,ROC曲线下的平均面积为0.79,提高了1.74%。
{"title":"Federated Learning for Site Aware Chest Radiograph Screening","authors":"A. Chakravarty, Avik Kar, Ramanathan Sethuraman, D. Sheet","doi":"10.1109/ISBI48211.2021.9433876","DOIUrl":"https://doi.org/10.1109/ISBI48211.2021.9433876","url":null,"abstract":"The shortage of Radiologists is inspiring the development of Deep Learning (DL) based solutions for detecting cardio, thoracic and pulmonary pathologies in Chest radiographs through multi-institutional collaborations. However, sharing the training data across multiple sites is often impossible due to privacy, ownership and technical challenges. Although Federated Learning (FL) has emerged as a solution to this, the large variations in disease prevalence and co-morbidity distributions across the sites may hinder proper training. We propose a DL architecture with a Convolutional Neural Network (CNN) followed by a Graph Neural Network (GNN) to address this issue. The CNN-GNN model is trained by modifying the Federated Averaging algorithm. The CNN weights are shared across all sites to extract robust features while separate GNN models are trained at each site to leverage the local co-morbidity dependencies for multi-label disease classification. The CheXpert dataset is partitioned across five sites to simulate the FL set up. Federated training did not show any significant drop in performance over centralized training. The site-specific GNN models also demonstrated their efficacy in modelling local disease co-occurrence statistics leading to an average area under the ROC curve of 0.79 with a 1.74% improvement.","PeriodicalId":372939,"journal":{"name":"2021 IEEE 18th International Symposium on Biomedical Imaging (ISBI)","volume":"74 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2021-04-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"121683412","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 12
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。
{"title":"Deep Learning For Light Field Microscopy Using Physics-Based Models","authors":"Herman Verinaz-Jadan, P. Song, Carmel L. Howe, Peter Quicke, Amanda J. Foust, P. Dragotti","doi":"10.1109/ISBI48211.2021.9434004","DOIUrl":"https://doi.org/10.1109/ISBI48211.2021.9434004","url":null,"abstract":"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.","PeriodicalId":372939,"journal":{"name":"2021 IEEE 18th International Symposium on Biomedical Imaging (ISBI)","volume":"69 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2021-04-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"121757157","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 5
Learning Few-Shot Chest X-Ray Diagnosis Using Images From The Published Scientific Literature 利用已发表的科学文献中的图像学习少量胸部x射线诊断
Pub Date : 2021-04-13 DOI: 10.1109/ISBI48211.2021.9434059
Angshuman Paul, Thomas C. Shen, Yifan Peng, Zhiyong Lu, R. Summers
A trained radiologist may learn the visual presentation of a new disease by looking at a few relevant image examples in research articles. However, training a machine learning model in such a manner is an arduous task not only due to the small number of labeled training images but also for the low resolution of such images. We design a few-shot learning method that can diagnose new diseases from chest x-rays utilizing only a few relevant labeled x-ray images from the published literature. Our method uses prior knowledge about other diseases for feature extraction from x-rays of new diseases. We formulate a classifier that is initially trained with a few labeled feature vectors corresponding to low-resolution images from the PubMed Central. The classifier is subsequently re-trained using unlabeled feature vectors corresponding to high-resolution x-ray images. Experiments on publicly available datasets show the superiority of the proposed method to several state-of-the-art few-shot learning techniques for chest x-ray diagnosis.
一个训练有素的放射科医生可以通过研究文章中一些相关的图像例子来学习一种新疾病的视觉表现。然而,以这种方式训练机器学习模型是一项艰巨的任务,不仅因为标记的训练图像数量少,而且这些图像的分辨率也很低。我们设计了一种少量学习方法,该方法可以仅利用已发表文献中的少量相关标记x射线图像从胸部x射线中诊断新的疾病。我们的方法利用其他疾病的先验知识对新疾病的x射线进行特征提取。我们制定了一个分类器,该分类器最初使用与来自PubMed Central的低分辨率图像对应的几个标记特征向量进行训练。随后使用对应于高分辨率x射线图像的未标记特征向量重新训练分类器。在公开可用的数据集上进行的实验表明,所提出的方法优于几种最先进的胸部x射线诊断的少镜头学习技术。
{"title":"Learning Few-Shot Chest X-Ray Diagnosis Using Images From The Published Scientific Literature","authors":"Angshuman Paul, Thomas C. Shen, Yifan Peng, Zhiyong Lu, R. Summers","doi":"10.1109/ISBI48211.2021.9434059","DOIUrl":"https://doi.org/10.1109/ISBI48211.2021.9434059","url":null,"abstract":"A trained radiologist may learn the visual presentation of a new disease by looking at a few relevant image examples in research articles. However, training a machine learning model in such a manner is an arduous task not only due to the small number of labeled training images but also for the low resolution of such images. We design a few-shot learning method that can diagnose new diseases from chest x-rays utilizing only a few relevant labeled x-ray images from the published literature. Our method uses prior knowledge about other diseases for feature extraction from x-rays of new diseases. We formulate a classifier that is initially trained with a few labeled feature vectors corresponding to low-resolution images from the PubMed Central. The classifier is subsequently re-trained using unlabeled feature vectors corresponding to high-resolution x-ray images. Experiments on publicly available datasets show the superiority of the proposed method to several state-of-the-art few-shot learning techniques for chest x-ray diagnosis.","PeriodicalId":372939,"journal":{"name":"2021 IEEE 18th International Symposium on Biomedical Imaging (ISBI)","volume":"59 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2021-04-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"121947765","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
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。
{"title":"Two-Stage Multi-Scale Mass Segmentation From Full Mammograms","authors":"Yutong Yan, Pierre-Henri Conze, G. Quellec, M. Lamard, B. Cochener, G. Coatrieux","doi":"10.1109/ISBI48211.2021.9433946","DOIUrl":"https://doi.org/10.1109/ISBI48211.2021.9433946","url":null,"abstract":"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.","PeriodicalId":372939,"journal":{"name":"2021 IEEE 18th International Symposium on Biomedical Imaging (ISBI)","volume":"52 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2021-04-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"122910848","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
Analysis Of Brain Functional Connectivity By Frequent Pattern Mining In Graphs. Application To The Characterization Of Murine Models 基于频繁模式挖掘的脑功能连通性分析。在小鼠模型表征中的应用
Pub Date : 2021-04-13 DOI: 10.1109/ISBI48211.2021.9434117
Aurélie Leborgne, F. Ber, Laetitia Degiorgis, L. Harsan, Stella Marc-Zwecker, V. Noblet
Functional Magnetic Resonance Imaging (fMRI) is an imaging technique that allows to explore brain function in vivo. Many methods dedicated to analyzing these data are based on graph modeling, each node corresponding to a brain region and the edges representing their functional link. The objective of this work is to investigate the interest of methods for extracting frequent pattern in graphs to compare these data between two populations. Results are presented in the context of the characterization of a mouse model of Alzheimer’s disease in comparison with a group of control mice.
功能磁共振成像(fMRI)是一种可以在体内探索大脑功能的成像技术。许多用于分析这些数据的方法都是基于图建模的,每个节点对应一个大脑区域,边缘表示它们的功能链接。这项工作的目的是研究在图中提取频繁模式的方法的兴趣,以比较两个种群之间的这些数据。结果是在阿尔茨海默病小鼠模型的特征与一组对照小鼠比较的背景下提出的。
{"title":"Analysis Of Brain Functional Connectivity By Frequent Pattern Mining In Graphs. Application To The Characterization Of Murine Models","authors":"Aurélie Leborgne, F. Ber, Laetitia Degiorgis, L. Harsan, Stella Marc-Zwecker, V. Noblet","doi":"10.1109/ISBI48211.2021.9434117","DOIUrl":"https://doi.org/10.1109/ISBI48211.2021.9434117","url":null,"abstract":"Functional Magnetic Resonance Imaging (fMRI) is an imaging technique that allows to explore brain function in vivo. Many methods dedicated to analyzing these data are based on graph modeling, each node corresponding to a brain region and the edges representing their functional link. The objective of this work is to investigate the interest of methods for extracting frequent pattern in graphs to compare these data between two populations. Results are presented in the context of the characterization of a mouse model of Alzheimer’s disease in comparison with a group of control mice.","PeriodicalId":372939,"journal":{"name":"2021 IEEE 18th International Symposium on Biomedical Imaging (ISBI)","volume":"9 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2021-04-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"124232122","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
Accurate 3d Kidney Segmentation Using Unsupervised Domain Translation And Adversarial Networks 使用无监督域翻译和对抗网络的精确3d肾脏分割
Pub Date : 2021-04-13 DOI: 10.1109/ISBI48211.2021.9434099
Wankang Zeng, Wenkang Fan, Rongzhen Chen, Zhuohui Zheng, Song Zheng, Jianhui Chen, Rong Liu, Q. Zeng, Zengqin Liu, Yinran Chen, Xióngbiao Luó
Computed tomography urography imaging is routinely performed to evaluate the kidneys. Kidney 3D segmentation and reconstruction from urographic images provides physicians with an intuitive visualization way to accurately diagnose and treat kidney diseases, particularly used in surgical planning and outcome analysis before and after kidney surgery. While 3D fully convolution networks have achieved a big success in medical image segmentation, they get trapped in clinical unseen data and cannot be adapted in deferent modalities with one training procedure. This study proposes an unsupervised domain adaptation or translation method with 2D networks to deeply learn urographic images for accurate kidney segmentation. We tested our proposed method on clinical urography data. The experimental results demonstrate our proposed method can resolve the domain shift problem of kidney segmentation and achieve the comparable or better results than supervised learning based segmentation methods.
计算机断层尿路成像是评估肾脏的常规方法。肾脏三维分割和重建尿路图像为医生提供了一种直观的可视化方法来准确诊断和治疗肾脏疾病,特别是用于肾脏手术前后的手术计划和结果分析。虽然3D全卷积网络在医学图像分割方面取得了巨大的成功,但它们被困在临床看不见的数据中,不能通过一个训练程序适应不同的模式。本研究提出一种基于二维网络的无监督域自适应或翻译方法,对尿路图像进行深度学习,实现肾脏的准确分割。我们用临床尿路造影数据检验了我们提出的方法。实验结果表明,该方法可以很好地解决肾脏分割的域移位问题,并取得与基于监督学习的分割方法相当或更好的分割效果。
{"title":"Accurate 3d Kidney Segmentation Using Unsupervised Domain Translation And Adversarial Networks","authors":"Wankang Zeng, Wenkang Fan, Rongzhen Chen, Zhuohui Zheng, Song Zheng, Jianhui Chen, Rong Liu, Q. Zeng, Zengqin Liu, Yinran Chen, Xióngbiao Luó","doi":"10.1109/ISBI48211.2021.9434099","DOIUrl":"https://doi.org/10.1109/ISBI48211.2021.9434099","url":null,"abstract":"Computed tomography urography imaging is routinely performed to evaluate the kidneys. Kidney 3D segmentation and reconstruction from urographic images provides physicians with an intuitive visualization way to accurately diagnose and treat kidney diseases, particularly used in surgical planning and outcome analysis before and after kidney surgery. While 3D fully convolution networks have achieved a big success in medical image segmentation, they get trapped in clinical unseen data and cannot be adapted in deferent modalities with one training procedure. This study proposes an unsupervised domain adaptation or translation method with 2D networks to deeply learn urographic images for accurate kidney segmentation. We tested our proposed method on clinical urography data. The experimental results demonstrate our proposed method can resolve the domain shift problem of kidney segmentation and achieve the comparable or better results than supervised learning based segmentation methods.","PeriodicalId":372939,"journal":{"name":"2021 IEEE 18th International Symposium on Biomedical Imaging (ISBI)","volume":"6 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2021-04-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"125385894","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
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。
{"title":"Characterizing The Uncertainty Of Label Noise In Systematic Ultrasound-Guided Prostate Biopsy","authors":"Golara Javadi, S. Samadi, Sharareh Bayat, Samira Sojoudi, Antonio Hurtado, Silvia D. Chang, Peter C. Black, P. Mousavi, P. Abolmaesumi","doi":"10.1109/ISBI48211.2021.9433765","DOIUrl":"https://doi.org/10.1109/ISBI48211.2021.9433765","url":null,"abstract":"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.","PeriodicalId":372939,"journal":{"name":"2021 IEEE 18th International Symposium on Biomedical Imaging (ISBI)","volume":"37 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2021-04-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"129977968","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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。
{"title":"Enhancing HARDI Reconstruction from Undersampled Data Via Multi-Context and Feature Inter-Dependency GAN","authors":"Ranjeet Ranjan Jha, Hritik Gupta, S. Pathak, W. Schneider, B. V. R. Kumar, A. Bhavsar, A. Nigam","doi":"10.1109/ISBI48211.2021.9434162","DOIUrl":"https://doi.org/10.1109/ISBI48211.2021.9434162","url":null,"abstract":"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.","PeriodicalId":372939,"journal":{"name":"2021 IEEE 18th International Symposium on Biomedical Imaging (ISBI)","volume":"10 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2021-04-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"130095999","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 7
Analysis Of Flat Fields In Edge Illumination Phase Contrast Imaging 边缘照明相衬成像中的平场分析
Pub Date : 2021-04-13 DOI: 10.1109/ISBI48211.2021.9433849
Ben Huyge, Jonathan G. Sanctorum, Nathanael Six, J. D. Beenhouwer, Jan Sijbers
One of the most commonly used correction methods in X-ray imaging is flat field correction, which corrects for systematic inconsistencies, such as differences in detector pixel response. In conventional X-ray imaging, flat fields are acquired by exposing the detector without any object in the X-ray beam. However, in edge illumination X-ray CT, which is an emerging phase contrast imaging technique, two masks are used to measure the refraction of the X-rays. These masks remain in place while the flat fields are acquired and thus influence the intensity of the flat fields. This influence is studied theoretically and validated experimentally using Monte Carlo simulations of an edge illumination experiment in GATE.
x射线成像中最常用的校正方法之一是平场校正,它校正系统的不一致性,例如探测器像素响应的差异。在传统的x射线成像中,通过在x射线束中不暴露任何物体的探测器来获得平坦场。然而,在边缘照明x射线CT中,这是一种新兴的相衬成像技术,使用两个掩模来测量x射线的折射。当获得平场时,这些掩模仍然存在,从而影响平场的强度。对这种影响进行了理论研究,并通过GATE的边缘照明实验蒙特卡罗模拟进行了实验验证。
{"title":"Analysis Of Flat Fields In Edge Illumination Phase Contrast Imaging","authors":"Ben Huyge, Jonathan G. Sanctorum, Nathanael Six, J. D. Beenhouwer, Jan Sijbers","doi":"10.1109/ISBI48211.2021.9433849","DOIUrl":"https://doi.org/10.1109/ISBI48211.2021.9433849","url":null,"abstract":"One of the most commonly used correction methods in X-ray imaging is flat field correction, which corrects for systematic inconsistencies, such as differences in detector pixel response. In conventional X-ray imaging, flat fields are acquired by exposing the detector without any object in the X-ray beam. However, in edge illumination X-ray CT, which is an emerging phase contrast imaging technique, two masks are used to measure the refraction of the X-rays. These masks remain in place while the flat fields are acquired and thus influence the intensity of the flat fields. This influence is studied theoretically and validated experimentally using Monte Carlo simulations of an edge illumination experiment in GATE.","PeriodicalId":372939,"journal":{"name":"2021 IEEE 18th International Symposium on Biomedical Imaging (ISBI)","volume":"4 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2021-04-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"124974531","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
Information Flow Through U-Nets U-Nets中的信息流
Pub Date : 2021-04-13 DOI: 10.1109/ISBI48211.2021.9433801
Suemin Lee, I. Bajić
Deep Neural Networks (DNNs) have become ubiquitous in medical image processing and analysis. Among them, U-Nets are very popular in various image segmentation tasks. Yet, little is known about how information flows through these networks and whether they are indeed properly designed for the tasks they are being proposed for. In this paper, we employ information-theoretic tools in order to gain insight into information flow through U-Nets. In particular, we show how mutual information between input/output and an intermediate layer can be a useful tool to understand information flow through various portions of a U-Net, assess its architectural efficiency, and even propose more efficient designs.
深度神经网络(dnn)在医学图像处理和分析中已经无处不在。其中,U-Nets在各种图像分割任务中非常流行。然而,对于信息如何在这些网络中流动,以及这些网络是否确实适合它们被提议执行的任务,人们所知甚少。在本文中,我们使用信息论工具来深入了解通过U-Nets的信息流。特别是,我们展示了输入/输出和中间层之间的相互信息如何成为理解U-Net各个部分的信息流、评估其架构效率、甚至提出更有效的设计的有用工具。
{"title":"Information Flow Through U-Nets","authors":"Suemin Lee, I. Bajić","doi":"10.1109/ISBI48211.2021.9433801","DOIUrl":"https://doi.org/10.1109/ISBI48211.2021.9433801","url":null,"abstract":"Deep Neural Networks (DNNs) have become ubiquitous in medical image processing and analysis. Among them, U-Nets are very popular in various image segmentation tasks. Yet, little is known about how information flows through these networks and whether they are indeed properly designed for the tasks they are being proposed for. In this paper, we employ information-theoretic tools in order to gain insight into information flow through U-Nets. In particular, we show how mutual information between input/output and an intermediate layer can be a useful tool to understand information flow through various portions of a U-Net, assess its architectural efficiency, and even propose more efficient designs.","PeriodicalId":372939,"journal":{"name":"2021 IEEE 18th International Symposium on Biomedical Imaging (ISBI)","volume":"57 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2021-04-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"131495400","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
期刊
2021 IEEE 18th International Symposium on Biomedical Imaging (ISBI)
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1