1.Brain image segmentation based on multi-weighted probabilistic atlas.
Lei ZHANG ; Minghui ZHANG ; Zhentai LU ; Qianjin FENG ; Wufan CHEN
Journal of Southern Medical University 2015;35(8):1143-1148
We propose a multi-weighted probabilistic atlas to obtain accurate, robust, and reliable segmentation. The local similarity measure is used as the weight to compute the probabilistic atlas, and the distance field is used as the weight to incorporate the locality information of the atlas; the self-similarity is used as the weight to incorporate the local information of target image to refine the probabilistic atlas. Experimental results with brain MRI images showed that the proposed algorithm outperforms the common brain image segmentation methods and achieved a median Dice coefficient of 87.1% on the left hippocampus and 87.6% on the right.
Algorithms
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Brain
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anatomy & histology
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Humans
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Magnetic Resonance Imaging
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Neuroimaging
2.Medical image segmentation based on guided filtering and multi-atlas.
Rui WEN ; Hongwen CHEN ; Lei ZHANG ; Zhentai LU
Journal of Southern Medical University 2015;35(9):1263-1267
A novel medical automatic image segmentation strategy based on guided filtering and multi-atlas is proposed to achieve accurate, smooth, robust, and reliable segmentation. This framework consists of 4 elements: the multi-atlas registration, which uses the atlas prior information; the label fusion, in which the similarity measure of the registration is used as the weight to fuse the warped label; the guided filtering, which uses the local information of the target image to correct the registration errors; and the threshold approaches used to obtain the segment result. The experimental results showed part among the 15 brain MRI images used to segment the hippocampus region, the proposed method achieved a median Dice coefficient of 86% on the left hippocampus and 87.4% on the right hippocampus. Compared with the traditional label fusion algorithm, the proposed algorithm outperforms the common brain image segmentation methods with a good efficiency and accuracy.
Algorithms
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Hippocampus
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anatomy & histology
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Humans
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Image Processing, Computer-Assisted
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methods
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Magnetic Resonance Imaging
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Neuroimaging
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Software
3.Comparison between approximate entropy and regional homogeneity for identification of irritable bowel syndrome based on functional magnetic resonance imaging.
Jiaofen NAN ; Liangliang ZHANG ; Qian ZHENG ; Minghui ZHANG ; Zhentai LU
Journal of Southern Medical University 2019;39(9):1023-1029
OBJECTIVE:
To compare the effectiveness and sensitivity of entropy and regional homogeneity (ReHo) for identifying irritable bowel syndrome (IBS) based on functional magnetic resonance imaging (fMRI).
METHODS:
Voxel-based approximate entropy (ApEn) was calculated based on findings of resting fMRI of 54 patients with IBS and 54 healthy control subjects. Feature selection was performed using independent sample -test, and support vector machine was then used to classify and identify different groups. The classification performance obtained from ApEn was compared with that from ReHo.
RESULTS:
Significant differences between the two groups were found in the left triangle part of inferior prefrontal gyrus, right angular gyrus of the inferior parietal lobule, left inferior temporal gyrus, left middle temporal gyrus, left lingual gyrus, bilateral middle occipital gyrus and bilateral superior occipital gyrus for ReHo ( < 0.05), and in the bilateral postcentral gyrus, right precentral gyrus, right inferior temporal gyrus, bilateral middle temporal gyrus and left superior occipital gyrus for ApEn ( < 0.05). ApEn consistently showed better performance than ReHo regardless of the variations in the number of features. The classification accuracy, specificity and sensitivity of ApEn were 93.5185%, 90.7407% and 96.2963%, respectively, as compared with 86.1111%, 85.1852% and 87.037% of ReHo.
CONCLUSIONS
Entropy analysis based on fMRI can be more sensitive and effective than ReHo for identification of IBS.
Brain
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diagnostic imaging
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Brain Mapping
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Case-Control Studies
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Entropy
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Humans
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Irritable Bowel Syndrome
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diagnostic imaging
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Magnetic Resonance Imaging
4.A fast adaptive active contour model based on local gray difference for parotid duct.
Xuan DENG ; Tianjun LAN ; Minghui ZHANG ; Zhifeng CHEN ; Qian TAO ; Zhentai LU
Journal of Southern Medical University 2018;38(12):1485-1491
OBJECTIVE:
To establish a fast adaptive active contour model based on local gray difference for parotid duct image segmentation.
METHODS:
On the basis of the LBF model, we added the mean difference of the local gray scale inside and outside the contour as the energy term of the driving evolution curve, and the local gray-scale variance difference was used to replace and as the control term of the energy parameter value. Two local similarity factors of different neighborhood sizes were introduced to correct the effects of image gray unevenness and boundary blur to improve the segmentation efficiency.
RESULTS:
During image segmentation, this algorithm allowed for adaptive adjustment of the evolution direction, velocity and the energy weight of the internal and external regions according to the difference of gray mean and variance between the internal and external regions. This algorithm was also capable of detecting the actual boundary in a complex gradient boundary region, thus enabling the evolution curve to approach the target boundary quickly and accurately.
CONCLUSIONS
The proposed algorithm is superior to the existing segmentation algorithms and allows fast and accurate segmentation of the parotid duct with well-preserved image details.
Algorithms
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Color
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Image Processing, Computer-Assisted
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Parotid Gland
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diagnostic imaging
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Salivary Ducts
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diagnostic imaging
5.A region-level contrastive learning-based deep model for glomerular ultrastructure segmentation on electron microscope images.
Guoyu LIN ; Zhentai ZHANG ; Yanmeng LU ; Jian GENG ; Zhitao ZHOU ; Lijun LU ; Lei CAO
Journal of Southern Medical University 2023;43(5):815-824
OBJECTIVE:
We propose a novel region- level self-supervised contrastive learning method USRegCon (ultrastructural region contrast) based on the semantic similarity of ultrastructures to improve the performance of the model for glomerular ultrastructure segmentation on electron microscope images.
METHODS:
USRegCon used a large amount of unlabeled data for pre- training of the model in 3 steps: (1) The model encoded and decoded the ultrastructural information in the image and adaptively divided the image into multiple regions based on the semantic similarity of the ultrastructures; (2) Based on the divided regions, the first-order grayscale region representations and deep semantic region representations of each region were extracted by region pooling operation; (3) For the first-order grayscale region representations, a grayscale loss function was proposed to minimize the grayscale difference within regions and maximize the difference between regions. For deep semantic region representations, a semantic loss function was introduced to maximize the similarity of positive region pairs and the difference of negative region pairs in the representation space. These two loss functions were jointly used for pre-training of the model.
RESULTS:
In the segmentation task for 3 ultrastructures of the glomerular filtration barrier based on the private dataset GlomEM, USRegCon achieved promising segmentation results for basement membrane, endothelial cells, and podocytes, with Dice coefficients of (85.69 ± 0.13)%, (74.59 ± 0.13)%, and (78.57 ± 0.16)%, respectively, demonstrating a good performance of the model superior to many existing image-level, pixel-level, and region-level self-supervised contrastive learning methods and close to the fully- supervised pre-training method based on the large- scale labeled dataset ImageNet.
CONCLUSION
USRegCon facilitates the model to learn beneficial region representations from large amounts of unlabeled data to overcome the scarcity of labeled data and improves the deep model performance for glomerular ultrastructure recognition and boundary segmentation.
Humans
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Electrons
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Endothelial Cells
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Learning
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Podocytes
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Kidney Diseases