SVM

SVM
  • 文章类型: Journal Article
    在建筑物的建造和拆除阶段,需要数据来做出有关管理废物的明智决策。然而,在大多数发展中国家,废物产生领域的数据可用性非常有限。这项研究的目的是采用基于人工智能(AI)的方法来开发可靠的模型,以预测德黑兰案例研究中的每月建筑和拆除废物(C&DW)生成。伊朗。我们使用各种AI算法训练了不同的预测模型,包括多层感知器神经网络,径向基函数神经网络,支持向量机,和自适应神经模糊推理系统(ANFIS)。根据调查结果,所有采用的人工智能算法对C&DW预测模型都表现出很高的预测性能。ANFIS模型,R2=0.96和RMSE=0.04209,被确定为更好地代表C和DW代的观察值的模型。ANFIS模型的更好效率可能是由于其有效增强了神经网络以基于模糊逻辑能力对主观变量进行建模。通过预测未来的废物数量,可以将开发的预测模型用作C&DW管理的政策和决策的有效工具。
    Data is needed for making informed decisions regarding managing waste in the time of construction and demolition phases of buildings. However, data availability is very limited in most developing countries in the area of waste generation. The objective of this study is to employ an artificial intelligence (AI)-based approach to develop a reliable model for forecasting monthly construction and demolition waste (C&DW) generation in the case study of Tehran, Iran. We have trained different prediction models using various AI algorithms, including multilayer perceptron neural network, radial basis function neural network, support vector machines, and adaptive neuro-fuzzy inference system (ANFIS). According to the findings, all employed AI algorithms demonstrated high prediction performance for C&DW forecasting models. The ANFIS model, with R2 = 0.96 and RMSE = 0.04209, was identified as the model that better represented the observed values of C&DW generation. The better efficiency of the ANFIS model could be due to its effective enhancement of neural networks to model subjective variables based on fuzzy logic capabilities. The developed prediction model can be employed as an efficient tool for policy and decision-making for C&DW management by predicting waste quantities in the future.
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  • 文章类型: Journal Article
    背景:肺癌的早期筛查和检测对于疾病的诊断和预后至关重要。在本文中,我们研究了血清拉曼光谱用于肺癌快速筛查的可行性。
    方法:收集45例肺癌患者的拉曼光谱,45例肺部良性病变,45名健康志愿者然后应用支持向量机(SVM)算法建立肺癌诊断模型。此外,对15个独立个体进行了外部验证,包括5名肺癌患者,5例肺部良性病变患者,5健康对照
    结果:诊断灵敏度,特异性,准确率为91.67%,92.22%,90.56%(肺癌与健康控制),92.22%,95.56%,93.33%(肺良性病变与健康)和80.00%,83.33%,80.83%(肺癌与良性肺病变),反复。在独立验证队列中,我们的模型显示所有样本分类正确.
    结论:因此,这项研究表明,血清拉曼光谱分析技术与SVM算法相结合,在肺癌的无创检测中具有巨大的潜力。
    BACKGROUND: Early screening and detection of lung cancer is essential for the diagnosis and prognosis of the disease. In this paper, we investigated the feasibility of serum Raman spectroscopy for rapid lung cancer screening.
    METHODS: Raman spectra were collected from 45 patients with lung cancer, 45 with benign lung lesions, and 45 healthy volunteers. And then the support vector machine (SVM) algorithm was applied to build a diagnostic model for lung cancer. Furthermore, 15 independent individuals were sampled for external validation, including 5 lung cancer patients, 5 benign lung lesion patients, and 5 healthy controls.
    RESULTS: The diagnostic sensitivity, specificity, and accuracy were 91.67%, 92.22%, 90.56% (lung cancer vs. healthy control), 92.22%,95.56%,93.33% (benign lung lesion vs. healthy) and 80.00%, 83.33%, 80.83% (lung cancer vs. benign lung lesion), repectively. In the independent validation cohort, our model showed that all the samples were classified correctly.
    CONCLUSIONS: Therefore, this study demonstrates that the serum Raman spectroscopy analysis technique combined with the SVM algorithm has great potential for the noninvasive detection of lung cancer.
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  • 文章类型: Journal Article
    目的:本研究旨在通过计算机辅助诊断(CAD)方法解决在医学应用中识别视网膜损伤的挑战。数据是从印度四家著名的眼科医院收集的,用于分析和模型开发。
    方法:数据来自Silchar医学院和医院(SMCH),阿拉维德眼科医院(泰米尔纳德邦),LV普拉萨德眼科医院(海得拉巴),和Medanta(Gurugram)。ResNet-101架构的修改版本,名为ResNet-RS,用于视网膜损伤识别。在这个修改后的架构中,最后一层的softmax函数被替换为支持向量机(SVM)。由此产生的模型,称为ResNet-RS-SVM,对每家医院的数据集进行了单独和集体的培训和评估。
    结果:所提出的ResNet-RS-SVM模型在来自不同医院的数据集中实现了较高的准确性:对于Aravind,为99.17%,LVPrasad的98.53%,Medanta为98.33%,和100%的SMCH。当集体考虑所有医院时,该模型的准确率为97.19%。
    结论:研究结果表明,ResNet-RS-SVM模型在从印度多家眼科医院收集的不同数据集中准确识别视网膜损伤的有效性。这种方法在计算机辅助诊断方面提出了有希望的进步,以改善视网膜疾病的检测和管理。
    OBJECTIVE: This study aims to address the challenge of identifying retinal damage in medical applications through a computer-aided diagnosis (CAD) approach. Data was collected from four prominent eye hospitals in India for analysis and model development.
    METHODS: Data was collected from Silchar Medical College and Hospital (SMCH), Aravind Eye Hospital (Tamil Nadu), LV Prasad Eye Hospital (Hyderabad), and Medanta (Gurugram). A modified version of the ResNet-101 architecture, named ResNet-RS, was utilized for retinal damage identification. In this modified architecture, the last layer\'s softmax function was replaced with a support vector machine (SVM). The resulting model, termed ResNet-RS-SVM, was trained and evaluated on each hospital\'s dataset individually and collectively.
    RESULTS: The proposed ResNet-RS-SVM model achieved high accuracies across the datasets from the different hospitals: 99.17% for Aravind, 98.53% for LV Prasad, 98.33% for Medanta, and 100% for SMCH. When considering all hospitals collectively, the model attained an accuracy of 97.19%.
    CONCLUSIONS: The findings demonstrate the effectiveness of the ResNet-RS-SVM model in accurately identifying retinal damage in diverse datasets collected from multiple eye hospitals in India. This approach presents a promising advancement in computer-aided diagnosis for improving the detection and management of retinal diseases.
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  • 文章类型: Journal Article
    根据世界卫生组织,自从冠状病毒病(COVID-19)出现以来,全世界已经记录了数百万人的感染和大量死亡。自2020年以来,许多计算机科学研究人员已经使用卷积神经网络(CNN)来开发有趣的框架来检测这种疾病。然而,从胸部X射线图像中提取的不良特征以及可用模型的高计算成本给准确和快速的COVID-19检测框架带来了困难。此外,糟糕的特征提取导致了“维度诅咒”的问题,这将对模型的性能产生负面影响。特征选择通常被认为是一种预处理机制,用于从数据挖掘过程中的所有特征的给定集合中找到最佳特征子集。因此,这项研究的主要目的是提供一种从胸部X线片中提取COVID-19特征的准确有效方法,该方法的计算成本也比早期方法低.为了达到规定的目标,我们设计了一种基于浅层常规神经网络(SCNN)的特征提取机制,并利用新开发的优化算法使用了一种有效的方法来选择特征,Q学习嵌入式正弦余弦算法(QLESCA)。支持向量机(SVM)被用作分类器。五个公开可用的胸部X射线图像数据集,由4848张COVID-19图像和8669张非COVID-19图像组成,用于训练和评估所提出的模型。QLESCA的性能是根据最近的9种优化算法进行评估的。所提出的方法能够实现97.8086%的最高精度,同时将特征数量从100个减少到38个。实验证明,通过选择相关特征,使用QLESCA作为降维技术,模型的准确性得到了提高。
    According to the World Health Organization, millions of infections and a lot of deaths have been recorded worldwide since the emergence of the coronavirus disease (COVID-19). Since 2020, a lot of computer science researchers have used convolutional neural networks (CNNs) to develop interesting frameworks to detect this disease. However, poor feature extraction from the chest X-ray images and the high computational cost of the available models introduce difficulties for an accurate and fast COVID-19 detection framework. Moreover, poor feature extraction has caused the issue of \'the curse of dimensionality\', which will negatively affect the performance of the model. Feature selection is typically considered as a preprocessing mechanism to find an optimal subset of features from a given set of all features in the data mining process. Thus, the major purpose of this study is to offer an accurate and efficient approach for extracting COVID-19 features from chest X-rays that is also less computationally expensive than earlier approaches. To achieve the specified goal, we design a mechanism for feature extraction based on shallow conventional neural network (SCNN) and used an effective method for selecting features by utilizing the newly developed optimization algorithm, Q-Learning Embedded Sine Cosine Algorithm (QLESCA). Support vector machines (SVMs) are used as a classifier. Five publicly available chest X-ray image datasets, consisting of 4848 COVID-19 images and 8669 non-COVID-19 images, are used to train and evaluate the proposed model. The performance of the QLESCA is evaluated against nine recent optimization algorithms. The proposed method is able to achieve the highest accuracy of 97.8086% while reducing the number of features from 100 to 38. Experiments prove that the accuracy of the model improves with the usage of the QLESCA as the dimensionality reduction technique by selecting relevant features.
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  • 文章类型: Journal Article
    基于机器学习的患者监测系统通常部署在远程服务器上以用于分析异构数据。虽然移动技术的最新进展为直接在移动设备上部署此类系统提供了新的机会,研究界并没有广泛研究开发和部署方面的挑战。在本文中,我们系统地研究了在移动设备上开发和部署基于机器学习的患者监护系统的每个阶段所面临的挑战.对于每一类挑战,我们提供了一些可以被研究人员使用的建议,系统设计者,以及开发基于移动的预测和监控系统的开发人员。我们的调查结果表明,当开发人员处理移动平台时,他们必须根据预测系统的分类和计算性能来评估预测系统。因此,我们提出了一种新的机器学习训练和部署方法,专门为移动平台量身定制,该方法包含了传统分类器性能之外的指标。
    Machine learning-based patient monitoring systems are generally deployed on remote servers for analyzing heterogeneous data. While recent advances in mobile technology provide new opportunities to deploy such systems directly on mobile devices, the development and deployment challenges are not being extensively studied by the research community. In this paper, we systematically investigate challenges associated with each stage of the development and deployment of a machine learning-based patient monitoring system on a mobile device. For each class of challenges, we provide a number of recommendations that can be used by the researchers, system designers, and developers working on mobile-based predictive and monitoring systems. The results of our investigation show that when developers are dealing with mobile platforms, they must evaluate the predictive systems based on its classification and computational performance. Accordingly, we propose a new machine learning training and deployment methodology specifically tailored for mobile platforms that incorporates metrics beyond traditional classifier performance.
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  • 文章类型: Journal Article
    物体识别表示系统识别物体的能力,图像中的人类或动物。在这个领域,这项工作对不同的分类方法进行了比较分析,旨在识别Tactode瓷砖。涵盖的方法包括:(i)使用HOG和SVM进行机器学习;(ii)使用CNNs进行深度学习,例如VGG16,VGG19,ResNet152,MobileNetV2,SSD和YOLOv4;(iii)将手工制作的特征与SIFT进行匹配,SURF,BRISK和ORB;和(iv)模板匹配。创建了一个数据集来训练基于学习的方法(i和ii),关于其他方法(iii和iv),使用模板数据集.为了评估识别方法的性能,构建了两个测试数据集:tactude_small和tactude_big,由288张和12,000张图片组成,持有2784个和96,000个感兴趣的地区进行分类,分别。SSD和YOLOv4是他们领域最差的方法,而ResNet152和MobileNetV2表明它们是强大的识别方法。SURF,ORB和BRISK表现出了很好的识别性能,而SIFT是这种方法中最差的。基于模板匹配的方法获得了合理的识别结果,落后于大多数其他方法。这项研究的前三种方法是:VGG16,对于tactodde_small和tactodde_big,准确率为99.96%和99.95%,分别;VGG19对相同数据集的准确率为99.96%和99.68%;HOG和SVM,这对于tactode_small和tactode_big达到99.93%的精度,同时在各自的数据集上显示0.323s和0.232s的平均执行时间,是总体上最快的方法。这项工作表明,VGG16是本案例研究的最佳选择,因为它最大限度地减少了两个测试数据集的错误分类。
    Object recognition represents the ability of a system to identify objects, humans or animals in images. Within this domain, this work presents a comparative analysis among different classification methods aiming at Tactode tile recognition. The covered methods include: (i) machine learning with HOG and SVM; (ii) deep learning with CNNs such as VGG16, VGG19, ResNet152, MobileNetV2, SSD and YOLOv4; (iii) matching of handcrafted features with SIFT, SURF, BRISK and ORB; and (iv) template matching. A dataset was created to train learning-based methods (i and ii), and with respect to the other methods (iii and iv), a template dataset was used. To evaluate the performance of the recognition methods, two test datasets were built: tactode_small and tactode_big, which consisted of 288 and 12,000 images, holding 2784 and 96,000 regions of interest for classification, respectively. SSD and YOLOv4 were the worst methods for their domain, whereas ResNet152 and MobileNetV2 showed that they were strong recognition methods. SURF, ORB and BRISK demonstrated great recognition performance, while SIFT was the worst of this type of method. The methods based on template matching attained reasonable recognition results, falling behind most other methods. The top three methods of this study were: VGG16 with an accuracy of 99.96% and 99.95% for tactode_small and tactode_big, respectively; VGG19 with an accuracy of 99.96% and 99.68% for the same datasets; and HOG and SVM, which reached an accuracy of 99.93% for tactode_small and 99.86% for tactode_big, while at the same time presenting average execution times of 0.323 s and 0.232 s on the respective datasets, being the fastest method overall. This work demonstrated that VGG16 was the best choice for this case study, since it minimised the misclassifications for both test datasets.
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  • 文章类型: Journal Article
    掌握乳腺癌(BC)的分子机制可以为深入了解BC病理提供依据。本研究探索了诊断BC的现有技术,比如乳房X线照相术,超声,磁共振成像(MRI),计算机断层扫描(CT),和正电子发射断层扫描(PET),并总结了现有癌症诊断的缺点。本文的目的是使用癌症基因组图谱(TCGA)和基因表达综合(GEO)的基因表达谱对BC样品和正常样品进行分类。本文提出的方法克服了传统诊断方法的一些缺点,可以更快速地进行BC诊断,灵敏度高,无辐射。本研究首先通过加权基因共表达网络分析(WGCNA)和差异表达分析(DEA)选择与癌症最相关的基因。然后,它使用蛋白质-蛋白质相互作用(PPI)网络筛选了23个hub基因。最后,它使用了支持向量机(SVM),决策树(DT),贝叶斯网络(BN),人工神经网络(ANN),卷积神经网络CNN-LeNet和CNN-AlexNet来处理23个hub基因的表达水平。对于基因表达谱,ANN模型在癌症样本分类中具有最佳性能。十次平均准确度为97.36%(±0.34%),F1值为0.8535(±0.0260),灵敏度为98.32%(±0.32%),特异性为89.59%(±3.53%),AUC为0.99。总之,该方法有效地对癌症样本和正常样本进行了分类,为今后癌症的早期诊断提供了合理的新思路。
    Mastering the molecular mechanism of breast cancer (BC) can provide an in-depth understanding of BC pathology. This study explored existing technologies for diagnosing BC, such as mammography, ultrasound, magnetic resonance imaging (MRI), computed tomography (CT), and positron emission tomography (PET) and summarized the disadvantages of the existing cancer diagnosis. The purpose of this article is to use gene expression profiles of The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) to classify BC samples and normal samples. The method proposed in this article triumphs over some of the shortcomings of traditional diagnostic methods and can conduct BC diagnosis more rapidly with high sensitivity and have no radiation. This study first selected the genes most relevant to cancer through weighted gene co-expression network analysis (WGCNA) and differential expression analysis (DEA). Then it used the protein-protein interaction (PPI) network to screen 23 hub genes. Finally, it used the support vector machine (SVM), decision tree (DT), Bayesian network (BN), artificial neural network (ANN), convolutional neural network CNN-LeNet and CNN-AlexNet to process the expression levels of 23 hub genes. For gene expression profiles, the ANN model has the best performance in the classification of cancer samples. The ten-time average accuracy is 97.36% (±0.34%), the F1 value is 0.8535 (±0.0260), the sensitivity is 98.32% (±0.32%), the specificity is 89.59% (±3.53%) and the AUC is 0.99. In summary, this method effectively classifies cancer samples and normal samples and provides reasonable new ideas for the early diagnosis of cancer in the future.
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  • 文章类型: Journal Article
    在过去的十年里,已经进行了许多研究来改进用于阿尔茨海默病(AD)诊断的计算机辅助系统。他们中的大多数最近开发了专注于从MRI中提取和组合特征的系统,PET,和CSF。在大多数情况下,他们获得了非常高的性能。然而,提高分类问题的性能是复杂的,特别是当模型的精度或其他性能测量高于90%时。在这项研究中,提出了一种新的方法来解决这个问题,特别是在阿尔茨海默病的诊断分类。这种方法在文献中是第一个,基于特征空间上的复制概念,而不是传统的样本空间。简而言之,所提出的方法的主要步骤包括提取,嵌入,探索特征的最佳子集。对于特征提取,我们采用VBM-SPM;对于嵌入特征,在特征上使用串联策略,以最终为每个主题创建一个特征向量。应用主成分分析提取新特征,形成一个低维的紧凑空间。通过复制选定的组件来应用一种新颖的方法,评估分类模型,并重复复制,直到性能分歧或收敛。所提出的方法旨在同时探索最显著的特征和最高预成型模型,将正常受试者与AD和轻度认知障碍(MCI)患者进行分类。在每个时代,通过支持向量机(SVM)分类器对候选特征的一小部分进行评估。该重复过程继续进行,直到达到最高性能。实验结果揭示了该特定分类问题在文献中报告的最高性能。我们得到了一个准确率为98.81%的模型,81.61%,AD和81.40%正常控制(NC),MCIvs.NC,和ADvs.MCI分类,分别。
    In the past decade, many studies have been conducted to advance computer-aided systems for Alzheimer\'s disease (AD) diagnosis. Most of them have recently developed systems concentrated on extracting and combining features from MRI, PET, and CSF. For the most part, they have obtained very high performance. However, improving the performance of a classification problem is complicated, specifically when the model\'s accuracy or other performance measurements are higher than 90%. In this study, a novel methodology is proposed to address this problem, specifically in Alzheimer\'s disease diagnosis classification. This methodology is the first of its kind in the literature, based on the notion of replication on the feature space instead of the traditional sample space. Briefly, the main steps of the proposed method include extracting, embedding, and exploring the best subset of features. For feature extraction, we adopt VBM-SPM; for embedding features, a concatenation strategy is used on the features to ultimately create one feature vector for each subject. Principal component analysis is applied to extract new features, forming a low-dimensional compact space. A novel process is applied by replicating selected components, assessing the classification model, and repeating the replication until performance divergence or convergence. The proposed method aims to explore most significant features and highest-preforming model at the same time, to classify normal subjects from AD and mild cognitive impairment (MCI) patients. In each epoch, a small subset of candidate features is assessed by support vector machine (SVM) classifier. This repeating procedure is continued until the highest performance is achieved. Experimental results reveal the highest performance reported in the literature for this specific classification problem. We obtained a model with accuracies of 98.81%, 81.61%, and 81.40% for AD vs. normal control (NC), MCI vs. NC, and AD vs. MCI classification, respectively.
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  • 文章类型: Journal Article
    Complex optical properties, such as non-pigment suspension and colored dissolved organic matter (CDOM), make it difficult to achieve accurate estimations of remotely sensed chlorophyll a (Chla) content of inland turbidity. Recent attempts have been made to estimate Chla based on red and near-infrared regions where non-pigment suspension and CDOM have little effect on water reflectance. The objective of this study is to validate the applicability of WV-2 imagery with existing effective estimation methods from MERIS when estimating Chla content in inland turbidity waters. The correlation analysis of measured Chla content and WV-2 imagery bands shows that the Chla sensitive bands of WV-2 are red edge, NIR 1, and NIR 2. The coastal band is designed for seawater Chla detection. However, the high correlation with turbidity data and low correlation with Chla made coastal band unsuitable for estimating Chla in inland waters. The high-resolution water body images were extracted by combining the spectral products (NDWI) with the spatial morphological products (sobel edge detection). The estimation results show that the accuracy of the single band and NDCI is not as good as the two-band method, three-band method, stepwise regression algorithm (SRA) and support vector machines (SVM). The SVM estimation accuracy was the highest with an R2, RMSE, and URMSE of 0.8387, 0.4714, and 19.11%, respectively. This study demonstrates that the two-band and three-band methods are effective for estimating Chla in inland water for WV-2 imagery. As a high-precision estimation method, SVM has great potential for inland turbidity water Chla estimation.
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  • 文章类型: Journal Article
    除草剂linuron(LIN)是一种具有抗雄激素作用模式的内分泌干扰物。这项研究的目的是(1)提高对硬骨膜卵巢中雄激素和抗雄激素信号传导的认识,以及(2)评估基因网络和机器学习使用转录组数据将LIN分类为抗雄激素的能力。将来自卵黄黑头鱼(FHM)的卵巢外植体暴露于三种浓度的5α-二氢睾酮(DHT),氟他胺(FLUT),或LIN为12h。暴露于DHT的卵巢显示17β-雌二醇(E2)的产生显着增加,而FLUT和LIN对E2没有影响。为了提高对卵巢雄激素受体信号传导的认识,使用通路分析构建了DHT和FLUT的互惠基因表达网络,这些数据表明类固醇代谢,翻译,DNA复制是通过卵巢中的AR信号调节的过程。子网络富集分析显示,与DHT相比,FLUT和LIN共有更多的受调控基因网络。使用来自不同鱼类的转录组数据集,机器学习算法将LIN与其他抗雄激素成功分类。这项研究提高了有关卵巢中对雄激素和抗雄激素反应的分子信号级联的知识,并提供了基因网络分析和机器学习可以使用从不同鱼类收集的实验转录组数据对优先化学物质进行分类的概念证明。
    The herbicide linuron (LIN) is an endocrine disruptor with an anti-androgenic mode of action. The objectives of this study were to (1) improve knowledge of androgen and anti-androgen signaling in the teleostean ovary and to (2) assess the ability of gene networks and machine learning to classify LIN as an anti-androgen using transcriptomic data. Ovarian explants from vitellogenic fathead minnows (FHMs) were exposed to three concentrations of either 5α-dihydrotestosterone (DHT), flutamide (FLUT), or LIN for 12h. Ovaries exposed to DHT showed a significant increase in 17β-estradiol (E2) production while FLUT and LIN had no effect on E2. To improve understanding of androgen receptor signaling in the ovary, a reciprocal gene expression network was constructed for DHT and FLUT using pathway analysis and these data suggested that steroid metabolism, translation, and DNA replication are processes regulated through AR signaling in the ovary. Sub-network enrichment analysis revealed that FLUT and LIN shared more regulated gene networks in common compared to DHT. Using transcriptomic datasets from different fish species, machine learning algorithms classified LIN successfully with other anti-androgens. This study advances knowledge regarding molecular signaling cascades in the ovary that are responsive to androgens and anti-androgens and provides proof of concept that gene network analysis and machine learning can classify priority chemicals using experimental transcriptomic data collected from different fish species.
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