HMGD: A High-Accuracy Model for Detection and Prediction of Respiratory Genetic Diseases

Kamal ElDahshan, H. Hefny, Iman Ahmed ElSayed
{"title":"HMGD: A High-Accuracy Model for Detection and Prediction of Respiratory Genetic Diseases","authors":"Kamal ElDahshan, H. Hefny, Iman Ahmed ElSayed","doi":"10.3844/jcssp.2024.649.657","DOIUrl":null,"url":null,"abstract":": Respiratory genetic diseases are considered a major participant in the reasons of death worldwide nowadays and were one of the major participants in helping in increasing the numbers of COVID-19 patients. It is considered one of the most alarming diseases affecting in particular the respiratory system. The journey of early detection of respiratory genetic diseases is considered to be very challenging today to assist in lessening the percentage rate of death since people with these diseases are more vulnerable to being infected by COVID-19 and other dangerous diseases than others. Also, it is considered a very difficult mission for medical practitioners because of the high requirement for expertise and knowledgeable practitioners. While, predicting or detecting respiratory genetic disease in an early phase has many gaps and lacks accuracy accommodated with speed as well; as a result any slight update in the accuracy accommodating speed will be considered of great improvement and importance which will later result in the reduction of the increasing number of genetically diseased patients as the well-known diseases of Alpha-1 antitrypsin deficiency, Cystic fibrosis, Kartagener syndrome and many other respiratory genetic diseases. In this study we will introduce a new hybrid-model approach (HMGD) based on merging two outstanding soft computing optimization algorithms which weren’t used before in neither detection nor prediction of diseases which are Extended Compact Genetic Algorithm (ECGA) and Compact Co-Evolutionary Algorithm (CCoEA); one for which ECGA will act for the feature selection phase and output will be fed to the CCoEA for feature optimization resulting in the certainty factor of the detected/predicted respiratory genetic disease. The model will be used through a graphical user-friendly interface built up especially for the model to analyze data, learn from that output data, and result in a tactile and touchable prediction/detection for the respiratory genetic disease. The HMGD model proved its reliability and outstanding performance over other known computational models by an accuracy of 98.27% for respiratory genetic diseases’ prediction in 1.03 sec, while an accuracy of 97.89% for respiratory genetic diseases’ detection in 1.4 sec. The model proved to achieve a higher level of accuracy in the detection or prediction of respiratory genetic diseases than other machine learning models.","PeriodicalId":40005,"journal":{"name":"Journal of Computer Science","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Computer Science","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3844/jcssp.2024.649.657","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

: Respiratory genetic diseases are considered a major participant in the reasons of death worldwide nowadays and were one of the major participants in helping in increasing the numbers of COVID-19 patients. It is considered one of the most alarming diseases affecting in particular the respiratory system. The journey of early detection of respiratory genetic diseases is considered to be very challenging today to assist in lessening the percentage rate of death since people with these diseases are more vulnerable to being infected by COVID-19 and other dangerous diseases than others. Also, it is considered a very difficult mission for medical practitioners because of the high requirement for expertise and knowledgeable practitioners. While, predicting or detecting respiratory genetic disease in an early phase has many gaps and lacks accuracy accommodated with speed as well; as a result any slight update in the accuracy accommodating speed will be considered of great improvement and importance which will later result in the reduction of the increasing number of genetically diseased patients as the well-known diseases of Alpha-1 antitrypsin deficiency, Cystic fibrosis, Kartagener syndrome and many other respiratory genetic diseases. In this study we will introduce a new hybrid-model approach (HMGD) based on merging two outstanding soft computing optimization algorithms which weren’t used before in neither detection nor prediction of diseases which are Extended Compact Genetic Algorithm (ECGA) and Compact Co-Evolutionary Algorithm (CCoEA); one for which ECGA will act for the feature selection phase and output will be fed to the CCoEA for feature optimization resulting in the certainty factor of the detected/predicted respiratory genetic disease. The model will be used through a graphical user-friendly interface built up especially for the model to analyze data, learn from that output data, and result in a tactile and touchable prediction/detection for the respiratory genetic disease. The HMGD model proved its reliability and outstanding performance over other known computational models by an accuracy of 98.27% for respiratory genetic diseases’ prediction in 1.03 sec, while an accuracy of 97.89% for respiratory genetic diseases’ detection in 1.4 sec. The model proved to achieve a higher level of accuracy in the detection or prediction of respiratory genetic diseases than other machine learning models.
HMGD:用于检测和预测呼吸系统遗传疾病的高精度模型
:呼吸系统遗传病被认为是当今世界死亡原因的主要组成部分,也是导致 COVID-19 患者人数增加的主要原因之一。它被认为是最令人担忧的疾病之一,尤其影响呼吸系统。呼吸系统遗传疾病的早期检测被认为是当今降低死亡率的一项极具挑战性的工作,因为这些疾病的患者比其他人更容易感染 COVID-19 和其他危险疾病。此外,由于对专业技术和知识渊博的从业人员要求很高,这对医疗从业人员来说也是一项非常艰巨的任务。而在早期预测或检测呼吸系统遗传疾病方面存在很多不足,缺乏准确性和快速性;因此,在准确性和快速性方面的任何微小改进都将被认为是巨大的进步和重要性,这将有助于减少日益增多的遗传疾病患者,如众所周知的阿尔法-1 抗胰蛋白酶缺乏症、囊性纤维化、卡塔格纳综合征和许多其他呼吸系统遗传疾病。在本研究中,我们将介绍一种新的混合模型方法(HMGD),该方法基于两种杰出的软计算优化算法(扩展紧凑遗传算法(ECGA)和紧凑协同进化算法(CCoEA))的合并,这两种算法以前从未用于疾病的检测或预测;其中,ECGA 将用于特征选择阶段,输出结果将反馈给 CCoEA 进行特征优化,从而得出所检测/预测的呼吸系统遗传疾病的确定系数。该模型将通过专门为其建立的图形化用户友好界面来分析数据,从输出数据中学习,并得出可触摸的呼吸系统遗传病预测/检测结果。与其他已知的计算模型相比,HMGD 模型证明了其可靠性和出色的性能,它在 1.03 秒内预测呼吸系统遗传疾病的准确率达到 98.27%,在 1.4 秒内检测呼吸系统遗传疾病的准确率达到 97.89%。事实证明,与其他机器学习模型相比,该模型在检测或预测呼吸系统遗传疾病方面的准确率更高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Journal of Computer Science
Journal of Computer Science Computer Science-Computer Networks and Communications
CiteScore
1.70
自引率
0.00%
发文量
92
期刊介绍: Journal of Computer Science is aimed to publish research articles on theoretical foundations of information and computation, and of practical techniques for their implementation and application in computer systems. JCS updated twelve times a year and is a peer reviewed journal covers the latest and most compelling research of the time.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信