基于新型卷积神经网络模型的 TP53 SNP 蛋白序列中的乳腺癌早期检测

Q2 Computer Science
Saifeddine Ben Nasr, Imen Messaoudi, Afef Elloumi Oueslati, Z. Lachiri
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引用次数: 0

摘要

导言:乳腺癌(BC)是最常见的癌症,也是妇女疾病死亡的第二大原因。乳腺癌病例与生殖器基因突变有关,这些基因突变有的是上一代遗传的,有的是后天获得的。如果能在第一阶段进行诊断,就能限制某些治疗方法的效果,节省费用,并最大限度地缩短诊断时间。这也有助于专家有针对性地采取最佳治疗方法,提高治愈率。然而,由于症状不明显,而且不建议对 40 岁以下的女性进行常规筛查,因此在患者中发现乳腺癌非常具有挑战性:目前,人们正努力利用机器学习和深度学习系统对乳腺癌进行早期检测。所提出的算法使用不同的数据类型来区分癌症和非癌症病例,如:乳腺放射摄影、超声波和核磁共振成像(MRI)图像。然后,将不同的学习工具应用于这些数据的分类任务。尽管分类率超过 90%,但所有这些方法的主要缺点是,它们只适用于出现癌症肿瘤之后,从而降低了治愈率。在数据方面,我们侧重于 17 号染色体中 TP53 基因的癌症和非癌症 SNP(单核苷酸多态性)蛋白序列。该基因被证明与不同的单氨基酸突变有关,我们将在此对此进行说明。我们提出的方法通过编码将 SNP 文本序列转换为数字向量。然后,利用连续小波变换生成 RGB scalogram 图像。对 Scalogram 图像进行颜色系数预处理,旨在创建四个不同的数据库。结果:在验证过程中,我们获得了良好的性能,特异性为 97.84%,灵敏度为 96.45%,总体准确率为 95.29%,平均运行时间为 12 分 3 秒。为了进一步提高这些结果,我们使用了 ORB 特征检测技术。结论:我们的方法可以在基因突变开始出现的患者中检测出疾病,从而大大节省时间和生命。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Breast cancer early detection in TP53 SNP protein sequences based on a new Convolutional Neural Network model
INTRODUCTION: Breast cancer (BC) is the most commonly occurring cancer and the second leading cause for women’s disease death. The BC cases are associated with genital mutations which are inherited from older generations or acquired overtime. If the diagnosis is done at the first stage, effects associated with certain treatments can be limited, costs can be saved and the diagnostic time can be minimized. This can also help specialists target the best treatment to increase the rate of cures. Nevertheless, its discovery in patients is very challenging due to silent symptoms aside from the fact the routine screening is not recommended for women under 40 years old.OBJECTIVES: Several efforts are aimed at the BC early detection using machine and deep learning systems. The proposed algorithms use different data types to distinguish between cancerous and non-cancerous cases; as: mammography, ultrasound and MRI (magnetic resonance imaging) images. Then, different learning tools were applied on this data for the classification task. Despite the classification rates which exceed 90%, the major drawback of all these methods is that they are applicable only after the appearance of the cancerous tumors, which reduces the cure rates.METHODS: We propose a new technique for early breast cancer screening. For the data, we focus on cancerous and non-cancerous SNP (Single Nucleotide Polymorphism) protein sequences of the TP53 gene in chromosome 17. This gene is shown to be linked to different single amino acid mutations on which we will shed light here. The method we propose transforms SNP textual sequences into digital vectors via coding. Then, RGB scalogram images are generated using the continuous wavelet transform. A pretreatment of color coefficients is applied to scalograms aiming at creating four different databases. Finally, a CNN deep learning network is used for the binary classification of cancerous and non-cancerous images.RESULTS: During the validation process, we reached good performance with specificity of 97.84%, sensitivity of 96.45%, an overall accuracy of 95.29% and an equal run time of 12 minutes 3 seconds. These values ensure the efficiency of our method.To enhance more these results, we used the ORB feature detection technique. Consequently, the classification rates have been improved to reach 95.9% as accuracyCONCLUSION: Our method will allow significant savings time and lives by detecting the disease in patients whose genetic mutations are beginning to appear.
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来源期刊
EAI Endorsed Transactions on Pervasive Health and Technology
EAI Endorsed Transactions on Pervasive Health and Technology Computer Science-Computer Science (miscellaneous)
CiteScore
3.50
自引率
0.00%
发文量
14
审稿时长
10 weeks
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