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1.
Sensors (Basel) ; 23(2)2023 Jan 10.
Artigo em Inglês | MEDLINE | ID: mdl-36679576

RESUMO

To provide accessible, intelligent, and efficient remote access such as the internet of things, rehabilitation, autonomous driving, virtual games, and healthcare, human action recognition (HAR) has gained much attention among computer vision researchers. Several methods have already been addressed to ensure effective and efficient action recognition based on different perspectives including data modalities, feature design, network configuration, and application domains. In this article, we design a new deep learning model by integrating criss-cross attention and edge convolution to extract discriminative features from the skeleton sequence for action recognition. The attention mechanism is applied in spatial and temporal directions to pursue the intra- and inter-frame relationships. Then, several edge convolutional layers are conducted to explore the geometric relationships among the neighboring joints in the human body. The proposed model is dynamically updated after each layer by recomputing the graph on the basis of k-nearest joints for learning local and global information in action sequences. We used publicly available benchmark skeleton datasets such as UTD-MHAD (University of Texas at Dallas multimodal human action dataset) and MSR-Action3D (Microsoft action 3D) to evaluate the proposed method. We also investigated the proposed method with different configurations of network architectures to assure effectiveness and robustness. The proposed method achieved average accuracies of 99.53% and 95.64% on the UTD-MHAD and MSR-Action3D datasets, respectively, outperforming state-of-the-art methods.


Assuntos
Algoritmos , Reconhecimento Automatizado de Padrão , Humanos , Reconhecimento Automatizado de Padrão/métodos , Redes Neurais de Computação , Esqueleto , Atividades Humanas
2.
Complex Intell Systems ; 9(2): 1265-1280, 2023.
Artigo em Inglês | MEDLINE | ID: mdl-36035628

RESUMO

DNA sequence similarity analysis is necessary for enormous purposes including genome analysis, extracting biological information, finding the evolutionary relationship of species. There are two types of sequence analysis which are alignment-based (AB) and alignment-free (AF). AB is effective for small homologous sequences but becomes NP-hard problem for long sequences. However, AF algorithms can solve the major limitations of AB. But most of the existing AF methods show high time complexity and memory consumption, less precision, and less performance on benchmark datasets. To minimize these limitations, we develop an AF algorithm using a 2D k - m e r count matrix inspired by the CGR approach. Then we shrink the matrix by analyzing the neighbors and then measure similarities using the best combinations of pairwise distance (PD) and phylogenetic tree methods. We also dynamically choose the value of k for k - m e r . We develop an efficient system for finding the positions of k - m e r in the count matrix. We apply our system in six different datasets. We achieve the top rank for two benchmark datasets from AFproject, 100% accuracy for two datasets (16 S Ribosomal, 18 Eutherian), and achieve a milestone for time complexity and memory consumption in comparison to the existing study datasets (HEV, HIV-1). Therefore, the comparative results of the benchmark datasets and existing studies demonstrate that our method is highly effective, efficient, and accurate. Thus, our method can be used with the top level of authenticity for DNA sequence similarity measurement.

3.
Sensors (Basel) ; 21(8)2021 Apr 11.
Artigo em Inglês | MEDLINE | ID: mdl-33920357

RESUMO

A colonoscopy is a medical examination used to check disease or abnormalities in the large intestine. If necessary, polyps or adenomas would be removed through the scope during a colonoscopy. Colorectal cancer can be prevented through this. However, the polyp detection rate differs depending on the condition and skill level of the endoscopist. Even some endoscopists have a 90% chance of missing an adenoma. Artificial intelligence and robot technologies for colonoscopy are being studied to compensate for these problems. In this study, we propose a self-supervised monocular depth estimation using spatiotemporal consistency in the colon environment. It is our contribution to propose a loss function for reconstruction errors between adjacent predicted depths and a depth feedback network that uses predicted depth information of the previous frame to predict the depth of the next frame. We performed quantitative and qualitative evaluation of our approach, and the proposed FBNet (depth FeedBack Network) outperformed state-of-the-art results for unsupervised depth estimation on the UCL datasets.


Assuntos
Adenoma , Inteligência Artificial , Colonoscópios , Colonoscopia , Retroalimentação , Humanos
4.
Genetics ; 165(3): 1117-26, 2003 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-14668369

RESUMO

Genetic analysis of nervous system function relies on the rigorous description of behavioral phenotypes. However, standard methods for classifying the behavioral patterns of mutant Caenorhabditis elegans rely on human observation and are therefore subjective and imprecise. Here we describe the application of machine learning to quantitatively define and classify the behavioral patterns of C. elegans nervous system mutants. We have used an automated tracking and image processing system to obtain measurements of a wide range of morphological and behavioral features from recordings of representative mutant types. Using principal component analysis, we represented the behavioral patterns of eight mutant types as data clouds distributed in multidimensional feature space. Cluster analysis using the k-means algorithm made it possible to quantitatively assess the relative similarities between different behavioral phenotypes and to identify natural phenotypic clusters among the data. Since the patterns of phenotypic similarity identified in this study closely paralleled the functional similarities of the mutant gene products, the complex phenotypic signatures obtained from these image data appeared to represent an effective diagnostic of the mutants' underlying molecular defects.


Assuntos
Caenorhabditis elegans/fisiologia , Animais , Caenorhabditis elegans/genética , Família Multigênica , Fenótipo
5.
J Neurosci Methods ; 118(1): 9-21, 2002 Jul 30.
Artigo em Inglês | MEDLINE | ID: mdl-12191753

RESUMO

Mutants with abnormal patterns of locomotion, also known as uncoordinated (Unc) mutants, have facilitated the genetic dissection of many important aspects of nervous system function and development in the nematode Caenorhabditis elegans. Although a large number of distinct classes of Unc mutants can be distinguished by an experienced observer, precise quantitative definitions of these classes have not been available. Here we describe a new approach for using automatically-acquired image data to quantify the locomotion patterns of wild-type and mutant worms. We designed an automated tracking and imaging system capable of following an individual animal for long time periods and saving a time-coded series of digital images representing its motion and body posture over the course of the recording. We have also devised methods for measuring specific features from these image data that can be used by the classification and regression tree classification algorithm to reliably identify the behavioral patterns of specific mutant types. Ultimately, these tools should make it possible to evaluate with quantitative precision the behavioral phenotypes of novel mutants, gene knockout lines, or pharmacological treatments.


Assuntos
Comportamento Animal/fisiologia , Caenorhabditis elegans/fisiologia , Processamento de Imagem Assistida por Computador/métodos , Atividade Motora/fisiologia , Algoritmos , Animais , Caenorhabditis elegans/genética , Atividade Motora/genética , Mutação , Fenótipo
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