SwePub
Sök i SwePub databas

  Utökad sökning

Träfflista för sökning "WFRF:(Gu Irene Yu Hua 1953) "

Sökning: WFRF:(Gu Irene Yu Hua 1953)

  • Resultat 1-10 av 227
Sortera/gruppera träfflistan
   
NumreringReferensOmslagsbildHitta
1.
  • Fu, Keren, 1988, et al. (författare)
  • Adaptive Multi-Level Region Merging for Salient Object Detection
  • 2014
  • Ingår i: British Machine Vision Conference (BMVC) 2014. ; , s. 11 -
  • Konferensbidrag (refereegranskat)abstract
    • Most existing salient object detection algorithms face the problem of either under or over-segmenting an image. More recent methods address the problem via multi-level segmentation. However, the number of segmentation levels is manually predetermined and only works well on specific class of images. In this paper, a new salient object detection scheme is presented based on adaptive multi-level region merging. A graph based merging scheme is developed to reassemble regions based on their shared contourstrength. This merging process is adaptive to complete contours of salient objects that can then be used for global perceptual analysis, e.g., foreground/ground separation. Such contour completion is enhanced by graph-based spectral decomposition. We show that even though simple region saliency measurements are adopted for each region, encouraging performance can be obtained after across-level integration. Experiments by comparing with 13 existing methods on three benchmark datasets including MSRA-1000, SOD and SED show the proposed method results in uniform object enhancement and achieves state-of-the-art performance.
  •  
2.
  • Fu, Keren, 1988, et al. (författare)
  • One-class support vector machine-assisted robust tracking
  • 2013
  • Ingår i: Journal of Electronic Imaging. - 1017-9909. ; 22:2, s. 11-
  • Tidskriftsartikel (refereegranskat)abstract
    • Recently, tracking is regarded as a binary classification problem by discriminative tracking methods. However, such binary classification may not fully handle the outliers, which may cause drifting. We argue that tracking may be regarded as one-class problem, which avoids gathering limited negative samples for background description. Inspired by the fact the positive feature space generatedby one-class support vector machine (SVM) is bounded by a closed hyper sphere, we propose a tracking method utilizing one-class SVMs that adopt histograms of oriented gradient and 2bit binary patterns as features. Thus, it is called the one-class SVM tracker (OCST). Simultaneously, an efficient initialization and online updating scheme is proposed. Extensive experimental results prove that OCST outperforms some state-of-the-art discriminative tracking methods that tackle the problem using binary classifiers on providing accurate tracking and alleviating serious drifting.
  •  
3.
  • Fu, Keren, 1988, et al. (författare)
  • One-Class SVM Assisted Accurate Tracking
  • 2012
  • Ingår i: 6th ACM/IEEE Int'l Conf on Distributed Smart Cameras (ICDSC 12), Oct 30 - Nov.2, 2012, Hong Kong. ; , s. 6 pages-
  • Konferensbidrag (refereegranskat)abstract
    • Recently, tracking is regarded as a binary classification problem by discriminative tracking methods. However, such binary classification may not fully handle the outliers, which may cause drifting. In this paper, we argue that tracking may be regarded as one-class problem, which avoids gathering limited negative samples for background description. Inspired by the fact the positive feature space generated by One-Class SVM is bounded by a closed sphere, we propose a novel tracking method utilizing One-Class SVMs that adopt HOG and 2 bit-BP as features, called One-Class SVM Tracker (OCST). Simultaneously an efficient initialization and online updating scheme is alsoproposed. Extensive experimental results prove that OCST outperforms some state-of-the-art discriminative tracking methods on providing accurate tracking and alleviating serious drifting.
  •  
4.
  • Ali, Muhaddisa Barat, 1986, et al. (författare)
  • A Feasibility Study on Deep Learning Based Brain Tumor Segmentation Using 2D Ellipse Box Areas.
  • 2022
  • Ingår i: Sensors (Basel, Switzerland). - : MDPI AG. - 1424-8220. ; 22:14
  • Tidskriftsartikel (refereegranskat)abstract
    • In most deep learning-based brain tumor segmentation methods, training the deep network requires annotated tumor areas. However, accurate tumor annotation puts high demands on medical personnel. The aim of this study is to train a deep network for segmentation by using ellipse box areas surrounding the tumors. In the proposed method, the deep network is trained by using a large number of unannotated tumor images with foreground (FG) and background (BG) ellipse box areas surrounding the tumor and background, and a small number of patients (<20) with annotated tumors. The training is conducted by initial training on two ellipse boxes on unannotated MRIs, followed by refined training on a small number of annotated MRIs. We use a multi-stream U-Net for conducting our experiments, which is an extension of the conventional U-Net. This enables the use of complementary information from multi-modality (e.g., T1, T1ce, T2, and FLAIR) MRIs. To test the feasibility of the proposed approach, experiments and evaluation were conducted on two datasets for glioma segmentation. Segmentation performance on the test sets is then compared with those used on the same network but trained entirely by annotated MRIs. Our experiments show that the proposed method has obtained good tumor segmentation results on the test sets, wherein the dice score on tumor areas is (0.8407, 0.9104), and segmentation accuracy on tumor areas is (83.88%, 88.47%) for the MICCAI BraTS'17 and US datasets, respectively. Comparing the segmented results by using the network trained by all annotated tumors, the drop in the segmentation performance from the proposed approach is (0.0594, 0.0159) in the dice score, and (8.78%, 2.61%) in segmented tumor accuracy for MICCAI and US test sets, which is relatively small. Our case studies have demonstrated that training the network for segmentation by using ellipse box areas in place of all annotated tumors is feasible, and can be considered as an alternative, which is a trade-off between saving medical experts' time annotating tumors and a small drop in segmentation performance.
  •  
5.
  • Ali, Muhaddisa Barat, 1986, et al. (författare)
  • A novel federated deep learning scheme for glioma and its subtype classification
  • 2023
  • Ingår i: Frontiers in Neuroscience. - 1662-4548 .- 1662-453X. ; 17
  • Tidskriftsartikel (refereegranskat)abstract
    • Background: Deep learning (DL) has shown promising results in molecular-based classification of glioma subtypes from MR images. DL requires a large number of training data for achieving good generalization performance. Since brain tumor datasets are usually small in size, combination of such datasets from different hospitals are needed. Data privacy issue from hospitals often poses a constraint on such a practice. Federated learning (FL) has gained much attention lately as it trains a central DL model without requiring data sharing from different hospitals. Method: We propose a novel 3D FL scheme for glioma and its molecular subtype classification. In the scheme, a slice-based DL classifier, EtFedDyn, is exploited which is an extension of FedDyn, with the key differences on using focal loss cost function to tackle severe class imbalances in the datasets, and on multi-stream network to exploit MRIs in different modalities. By combining EtFedDyn with domain mapping as the pre-processing and 3D scan-based post-processing, the proposed scheme makes 3D brain scan-based classification on datasets from different dataset owners. To examine whether the FL scheme could replace the central learning (CL) one, we then compare the classification performance between the proposed FL and the corresponding CL schemes. Furthermore, detailed empirical-based analysis were also conducted to exam the effect of using domain mapping, 3D scan-based post-processing, different cost functions and different FL schemes. Results: Experiments were done on two case studies: classification of glioma subtypes (IDH mutation and wild-type on TCGA and US datasets in case A) and glioma grades (high/low grade glioma HGG and LGG on MICCAI dataset in case B). The proposed FL scheme has obtained good performance on the test sets (85.46%, 75.56%) for IDH subtypes and (89.28%, 90.72%) for glioma LGG/HGG all averaged on five runs. Comparing with the corresponding CL scheme, the drop in test accuracy from the proposed FL scheme is small (−1.17%, −0.83%), indicating its good potential to replace the CL scheme. Furthermore, the empirically tests have shown that an increased classification test accuracy by applying: domain mapping (0.4%, 1.85%) in case A; focal loss function (1.66%, 3.25%) in case A and (1.19%, 1.85%) in case B; 3D post-processing (2.11%, 2.23%) in case A and (1.81%, 2.39%) in case B and EtFedDyn over FedAvg classifier (1.05%, 1.55%) in case A and (1.23%, 1.81%) in case B with fast convergence, which all contributed to the improvement of overall performance in the proposed FL scheme. Conclusion: The proposed FL scheme is shown to be effective in predicting glioma and its subtypes by using MR images from test sets, with great potential of replacing the conventional CL approaches for training deep networks. This could help hospitals to maintain their data privacy, while using a federated trained classifier with nearly similar performance as that from a centrally trained one. Further detailed experiments have shown that different parts in the proposed 3D FL scheme, such as domain mapping (make datasets more uniform) and post-processing (scan-based classification), are essential.
  •  
6.
  • Ali, Muhaddisa Barat, 1986, et al. (författare)
  • Domain Mapping and Deep Learning from Multiple MRI Clinical Datasets for Prediction of Molecular Subtypes in Low Grade Gliomas
  • 2020
  • Ingår i: Brain Sciences. - : MDPI AG. - 2076-3425. ; 10:7, s. 1-20
  • Tidskriftsartikel (refereegranskat)abstract
    • Brain tumors, such as low grade gliomas (LGG), are molecularly classified which require the surgical collection of tissue samples. The pre-surgical or non-operative identification of LGG molecular type could improve patient counseling and treatment decisions. However, radiographic approaches to LGG molecular classification are currently lacking, as clinicians are unable to reliably predict LGG molecular type using magnetic resonance imaging (MRI) studies. Machine learning approaches may improve the prediction of LGG molecular classification through MRI, however, the development of these techniques requires large annotated data sets. Merging clinical data from different hospitals to increase case numbers is needed, but the use of different scanners and settings can affect the results and simply combining them into a large dataset often have a significant negative impact on performance. This calls for efficient domain adaption methods. Despite some previous studies on domain adaptations, mapping MR images from different datasets to a common domain without affecting subtitle molecular-biomarker information has not been reported yet. In this paper, we propose an effective domain adaptation method based on Cycle Generative Adversarial Network (CycleGAN). The dataset is further enlarged by augmenting more MRIs using another GAN approach. Further, to tackle the issue of brain tumor segmentation that requires time and anatomical expertise to put exact boundary around the tumor, we have used a tight bounding box as a strategy. Finally, an efficient deep feature learning method, multi-stream convolutional autoencoder (CAE) and feature fusion, is proposed for the prediction of molecular subtypes (1p/19q-codeletion and IDH mutation). The experiments were conducted on a total of 161 patients consisting of FLAIR and T1 weighted with contrast enhanced (T1ce) MRIs from two different institutions in the USA and France. The proposed scheme is shown to achieve the test accuracy of 74.81% on 1p/19q codeletion and 81.19% on IDH mutation, with marked improvement over the results obtained without domain mapping. This approach is also shown to have comparable performance to several state-of-the-art methods.
  •  
7.
  • Ali, Muhaddisa Barat, 1986, et al. (författare)
  • Multi-stream Convolutional Autoencoder and 2D Generative Adversarial Network for Glioma Classification
  • 2019
  • Ingår i: Lecture Notes in Computer Science (including subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics). - Cham : Springer International Publishing. - 1611-3349 .- 0302-9743. ; 11678 LNCS, s. 234-245
  • Konferensbidrag (refereegranskat)abstract
    • Diagnosis and timely treatment play an important role in preventing brain tumor growth. Deep learning methods have gained much attention lately. Obtaining a large amount of annotated medical data remains a challenging issue. Furthermore, high dimensional features of brain images could lead to over-fitting. In this paper, we address the above issues. Firstly, we propose an architecture for Generative Adversarial Networks to generate good quality synthetic 2D MRIs from multi-modality MRIs (T1 contrast-enhanced, T2, FLAIR). Secondly, we propose a deep learning scheme based on 3-streams of Convolutional Autoencoders (CAEs) followed by sensor information fusion. The rational behind using CAEs is that it may improve glioma classification performance (as comparing with conventional CNNs), since CAEs offer noise robustness and also efficient feature reduction hence possibly reduce the over-fitting. A two-round training strategy is also applied by pre-training on GAN augmented synthetic MRIs followed by refined-training on original MRIs. Experiments on BraTS 2017 dataset have demonstrated the effectiveness of the proposed scheme (test accuracy 92.04%). Comparison with several exiting schemes has provided further support to the proposed scheme.
  •  
8.
  • Ali, Muhaddisa Barat, 1986, et al. (författare)
  • Prediction of glioma‑subtypes: comparison of performance on a DL classifier using bounding box areas versus annotated tumors
  • 2022
  • Ingår i: BioMedical Engineering Online. - : Springer Science and Business Media LLC. - 1475-925X .- 2524-4426. ; 4
  • Tidskriftsartikel (refereegranskat)abstract
    • Background: For brain tumors, identifying the molecular subtypes from magnetic resonance imaging (MRI) isdesirable, but remains a challenging task. Recent machine learning and deep learning (DL) approaches may help theclassification/prediction of tumor subtypes through MRIs. However, most of these methods require annotated datawith ground truth (GT) tumor areas manually drawn by medical experts. The manual annotation is a time consumingprocess with high demand on medical personnel. As an alternative automatic segmentation is often used. However, itdoes not guarantee the quality and could lead to improper or failed segmented boundaries due to differences in MRIacquisition parameters across imaging centers, as segmentation is an ill‑defined problem. Analogous to visual objecttracking and classification, this paper shifts the paradigm by training a classifier using tumor bounding box areas inMR images. The aim of our study is to see whether it is possible to replace GT tumor areas by tumor bounding boxareas (e.g. ellipse shaped boxes) for classification without a significant drop in performance.Method: In patients with diffuse gliomas, training a deep learning classifier for subtype prediction by employ‑ing tumor regions of interest (ROIs) using ellipse bounding box versus manual annotated data. Experiments wereconducted on two datasets (US and TCGA) consisting of multi‑modality MRI scans where the US dataset containedpatients with diffuse low‑grade gliomas (dLGG) exclusively.Results: Prediction rates were obtained on 2 test datasets: 69.86% for 1p/19q codeletion status on US dataset and79.50% for IDH mutation/wild‑type on TCGA dataset. Comparisons with that of using annotated GT tumor data fortraining showed an average of 3.0% degradation (2.92% for 1p/19q codeletion status and 3.23% for IDH genotype).Conclusion: Using tumor ROIs, i.e., ellipse bounding box tumor areas to replace annotated GT tumor areas for train‑ing a deep learning scheme, cause only a modest decline in performance in terms of subtype prediction. With moredata that can be made available, this may be a reasonable trade‑off where decline in performance may be counter‑acted with more data.
  •  
9.
  • Alipoor, Mohammad, 1983, et al. (författare)
  • A Novel Framework for repeated measurements in diffusion tensor imaging
  • 2016
  • Ingår i: 3rd (ACM) Int'l Conf. on Biomedical and Bioinformatics Engineering (ICBBE 2016). - New York, NY, USA : ACM. - 9781450348249 ; Part F125793, s. 1-6
  • Konferensbidrag (refereegranskat)abstract
    • In the context of diffusion tensor imaging (DTI), the utility of making repeated measurements in each diffusion sensitizing direction has been the subject of numerous stud-ies. One can estimate the true signal value using either the raw complex-valued data or the real-valued magnitudesignal. While conventional methods focus on the former strategy, this paper proposes a new framework for acquiring/processing repeated measurements based on the latter strategy. The aim is to enhance the DTI processing pipeline by adding a diffusion signal estimator (DSE). This permits us to exploit the knowledge of the noise distribution to estimate the true signal value in each direction. An extensive study of the proposed framework, including theoretical analysis, experiments with synthetic data, performance evaluation and comparisons is presented.Our results show that the precision of estimated diffusionparameters is dependent on the number of available samplesand the manner in which the DSE accounts for noise. Theproposed framework improves the precision in estimationof diffusion parameters given a sufficient number of uniquemeasurements. This encourages future work with rich realdatasets and downstream applications.
  •  
10.
  • Alipoor, Mohammad, 1983, et al. (författare)
  • Determinant of the information matrix: a new rotation invariant optimality metric to design gradient encoding schemes
  • 2015
  • Ingår i: 12th IEEE International Symposium on Biomedical Imaging, ISBI 2015, Brooklyn, United States, 16-19 April 2015. - 1945-8452. - 9781479923748 ; 2015-July, s. 462-465
  • Konferensbidrag (refereegranskat)abstract
    • Minimum condition number (CN) gradient encoding schemewas introduced to diffusion MRI community more than adecade ago. It’s computation requires tedious numerical optimization which usually leads to sub-optimal solutions. TheCN does not reflect any benefits in acquiring more measurements, i.e. it’s optimal value is constant for any numberof measurements. Further, it is variable under rotation. Inthis paper we (i) propose an accurate method to computeminimum condition number scheme; and (ii) introduce determinant of the information matrix (DIM) as a new optimality metric that scales with number of measurements anddoes reflect what one would gain from acquiring more measurements. Theoretical analysis shows that DIM is rotationinvariant. Evaluations on state-of-the-art encoding schemesproves the relevance and superiority of the proposed metriccompared to condition number.
  •  
Skapa referenser, mejla, bekava och länka
  • Resultat 1-10 av 227
Typ av publikation
konferensbidrag (146)
tidskriftsartikel (73)
bokkapitel (5)
rapport (1)
bok (1)
forskningsöversikt (1)
visa fler...
visa färre...
Typ av innehåll
refereegranskat (213)
övrigt vetenskapligt/konstnärligt (13)
populärvet., debatt m.m. (1)
Författare/redaktör
Gu, Irene Yu-Hua, 19 ... (227)
Bollen, Mathias, 196 ... (29)
Yang, Jie (25)
Yun, Yixiao, 1987 (24)
Bollen, Math (20)
Khan, Zulfiqar Hasan ... (20)
visa fler...
Styvaktakis, Emmanou ... (17)
Backhouse, Andrew, 1 ... (15)
Jakola, Asgeir Store (12)
Bollen, Math H. J. (10)
Alipoor, Mohammad, 1 ... (10)
Wang, Tiesheng, 1975 (10)
Li, L. (9)
Mehnert, Andrew, 196 ... (7)
Ali, Muhaddisa Barat ... (6)
Bagheri, Azam (6)
Viberg, Mats, 1961 (5)
Gong, C. (4)
Maier, Stephan E, 19 ... (4)
Huang, W (4)
Starck, Göran (3)
de Oliveira, Roger A ... (3)
Berger, Mitchel S (3)
Nilsson, Daniel, 197 ... (3)
Axelberg, P. (3)
Axelberg, Peter G.V. ... (3)
Bengtsson, Tomas, 19 ... (3)
Berlijn, Sonja M. (3)
Gutman, Igor (3)
Berlijn, Sonja (3)
Chen, Peiyuan, 1983 (3)
Rönnberg, Sarah (2)
Fredriksson, Jonas, ... (2)
Widhalm, Georg (2)
Vecchio, Tomás Gomez (2)
Lilja, Y (2)
Kahl, Fredrik, 1972 (2)
McKelvey, Tomas, 196 ... (2)
Gil-de-Castro, Auror ... (2)
Thordstein, Magnus (2)
Balouji, Ebrahim, 19 ... (2)
Nazari, Mahmood (2)
Meyer, Jan (2)
Lundberg, Magnus, 19 ... (2)
Häger, M. (2)
Santoso, Surya (2)
Ribeiro, Moises V (2)
Ribeiro, Paulo F. (2)
Flisberg, Anders, 19 ... (2)
Changrampadi, Mohame ... (2)
visa färre...
Lärosäte
Chalmers tekniska högskola (227)
Luleå tekniska universitet (25)
Göteborgs universitet (21)
Högskolan i Borås (2)
Lunds universitet (1)
Språk
Engelska (226)
Spanska (1)
Forskningsämne (UKÄ/SCB)
Naturvetenskap (177)
Teknik (155)
Medicin och hälsovetenskap (22)
Lantbruksvetenskap (1)
Samhällsvetenskap (1)

År

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Stäng

Kopiera och spara länken för att återkomma till aktuell vy