Deep Learning Techniques for Diagnosis of Lungs Cancer

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ID: 313280
2022
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Ranked #664 of 705 articles by views in Journal of Computing & Biomedical Informatics

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Abstract
Low_dose computed tomography (LDCT) scans are widely used to diagnose early cancers. Clinical studies show that low CT scans reduce lung cancer by 20% compared to standard radiography. However, conventional lowintensity CT scans are prone to overuse, high cost, and increased radiation exposure. This paper seeks to address these challenges by developing machine learning and in-depth case studies for automated cancer screening and assessing disease progression. The new split-method approach was first developed using two-sided select methods and machine learning methods. This method is designed to include ring nodes mounted on the ring bar but significantly reduce partition errors. Second, a neural network is being developed to classify clean nodes according to non-nodes. The simulation model integrates VGG, residual, and multi-network module design to enhance the dynamics of external collection components and various reception constraints. Third, the Hierarchical Semantic Convolutional Neural Network (HSCNN) is defined to form negative nodule rings. The semantic components, predicted to be equal to the deficit per node, facilitate the definition of this type and the improvement of visual acuity. Finally, the Bayesian design as well as the full-time Markov version have been improved. The decisionmaking process selects the exchange of information about the individual cancer, providing the basis for a special research study. Numerous experiments and results have shown the effectiveness of these experimental methods in improving and enhancing the efficiency of low-frequency CT programs.
Reference Key
imported_1777060226_69ebc982ae4e2 Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Ali Haider Khan
Journal Journal of Computing & Biomedical Informatics
Year 2022
DOI
10.56979/301/2022/36
URL
Keywords Keywords not found

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