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1.
Sci Rep ; 13(1): 8823, 2023 05 31.
Artigo em Inglês | MEDLINE | ID: mdl-37258631

RESUMO

Colorectal cancer (CRC) is the second leading cause of cancer death in the world, so digital pathology is essential for assessing prognosis. Due to the increasing resolution and quantity of whole slide images (WSIs), as well as the lack of annotated information, previous methodologies cannot be generalized as effective decision-making systems. Since deep learning (DL) methods can handle large-scale applications, they can provide a viable alternative to histopathology image (HI) analysis. DL architectures, however, may not be sufficient to classify CRC tissues based on anatomical histopathology data. A dilated ResNet (dResNet) structure and attention module are used to generate deep feature maps in order to classify multiple tissues in HIs. In addition, neighborhood component analysis (NCA) overcomes the constraint of computational complexity. Data is fed into a deep support vector machine (SVM) based on an ensemble learning algorithm called DeepSVM after the features have been selected. CRC-5000 and NCT-CRC-HE-100 K datasets were analyzed to validate and test the hybrid procedure. We demonstrate that the hybrid model achieves 98.75% and 99.76% accuracy on CRC datasets. The results showed that only pathologists' labels could successfully classify unseen WSIs. Furthermore, the hybrid deep learning method outperforms state-of-the-art approaches in terms of computational efficiency and time. Using the proposed mechanism for tissue analysis, it will be possible to correctly predict CRC based on accurate pathology image classification.


Assuntos
Neoplasias Colorretais , Aprendizado Profundo , Humanos , Algoritmos , Prognóstico , Patologistas , Neoplasias Colorretais/diagnóstico por imagem
2.
Comput Intell Neurosci ; 2023: 9379618, 2023.
Artigo em Inglês | MEDLINE | ID: mdl-36688224

RESUMO

The vast majority of sleep disturbances are caused by various types of sleep arousal. To diagnose sleep disorders and prevent health problems such as cardiovascular disease and cognitive impairment, sleep arousals must be accurately detected. Consequently, sleep specialists must spend considerable time and effort analyzing polysomnography (PSG) recordings to determine the level of arousal during sleep. The development of an automated sleep arousal detection system based on PSG would considerably benefit clinicians. We quantify the EEG-ECG by using Lyapunov exponents, fractals, and wavelet transforms to identify sleep stages and arousal disorders. In this paper, an efficient hybrid-learning method is introduced for the first time to detect and assess arousal incidents. Modified drone squadron optimization (mDSO) algorithm is used to optimize the support vector machine (SVM) with radial basis function (RBF) kernel. EEG-ECG signals are preprocessed samples from the SHHS sleep dataset and the PhysioBank challenge 2018. In comparison to other traditional methods for identifying sleep disorders, our physiological signals correlation innovation is much better than similar approaches. Based on the proposed model, the average error rate was less than 2%-7%, respectively, for two-class and four-class issues. Additionally, the proper classification of the five sleep stages is determined to be accurate 92.3% of the time. In clinical trials of sleep disorders, the hybrid-learning model technique based on EEG-ECG signal correlation features is effective in detecting arousals.


Assuntos
Transtornos do Despertar do Sono , Transtornos do Sono-Vigília , Humanos , Eletroencefalografia/métodos , Sono/fisiologia , Polissonografia/métodos , Transtornos do Sono-Vigília/diagnóstico
3.
Graefes Arch Clin Exp Ophthalmol ; 261(2): 391-399, 2023 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-36050474

RESUMO

PURPOSE: The study aims to classify the eyes with proliferative diabetic retinopathy (PDR) and non-proliferative diabetic retinopathy (NPDR) based on the optical coherence tomography angiography (OCTA) vascular density maps using a supervised machine learning algorithm. METHODS: OCTA vascular density maps (at superficial capillary plexus (SCP), deep capillary plexus (DCP), and total retina (R) levels) of 148 eyes from 78 patients with diabetic retinopathy (45 PDR and 103 NPDR) was used to classify the images to NPDR and PDR groups based on a supervised machine learning algorithm known as the support vector machine (SVM) classifier optimized by a genetic evolutionary algorithm. RESULTS: The implemented algorithm in three different models reached up to 85% accuracy in classifying PDR and NPDR in all three levels of vascular density maps. The deep retinal layer vascular density map demonstrated the best performance with a 90% accuracy in discriminating between PDR and NPDR. CONCLUSIONS: The current study on a limited number of patients with diabetic retinopathy demonstrated that a supervised machine learning-based method known as SVM can be used to differentiate PDR and NPDR patients using OCTA vascular density maps.


Assuntos
Diabetes Mellitus , Retinopatia Diabética , Humanos , Retinopatia Diabética/diagnóstico , Vasos Retinianos , Angiofluoresceinografia/métodos , Tomografia de Coerência Óptica/métodos , Densidade Microvascular , Retina , Aprendizado de Máquina
4.
IET Syst Biol ; 16(3-4): 120-131, 2022 05.
Artigo em Inglês | MEDLINE | ID: mdl-35790076

RESUMO

Malignancies and diseases of various genetic origins can be diagnosed and classified with microarray data. There are many obstacles to overcome due to the large size of the gene and the small number of samples in the microarray. A combination strategy for gene expression in a variety of diseases is described in this paper, consisting of two steps: identifying the most effective genes via soft ensembling and classifying them with a novel deep neural network. The feature selection approach combines three strategies to select wrapper genes and rank them according to the k-nearest neighbour algorithm, resulting in a very generalisable model with low error levels. Using soft ensembling, the most effective subsets of genes were identified from three microarray datasets of diffuse large cell lymphoma, leukaemia, and prostate cancer. A stacked deep neural network was used to classify all three datasets, achieving an average accuracy of 97.51%, 99.6%, and 96.34%, respectively. In addition, two previously unreported datasets from small, round blue cell tumors (SRBCTs)and multiple sclerosis-related brain tissue lesions were examined to show the generalisability of the model method.


Assuntos
Aprendizado Profundo , Neoplasias da Próstata , Algoritmos , Perfilação da Expressão Gênica/métodos , Humanos , Masculino , Análise de Sequência com Séries de Oligonucleotídeos/métodos
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