Design and Development of A Diagnostic System for Early Prediction of P53 Mutation Causing Cancer from Microscopic Biopsy Images

L. C, Namboori. P. K. Krıshnan
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Abstract

The major complication associated with cancer care is delayed cancer detection, which would also reduce the likelihood of survival. This situation could be resolved to some extend with an early diagnostic system. In the current study, designing an early detection system for TP53 mutation, which is a common primary mutation for most of the types of cancer, has been carried out using the ‘Pharmacogenomics’, ‘Gene expression profiling’ and ‘Deep imaging processing technique’. The input for the analysis is microscopic biopsy images collected from the ‘Expression atlas database’. The high level of expression of TP53 gene mutation has been observed in Breast and Ovarian cancers samples. The involvement of associated genes like BARD1, CHEK2, ATM, BRCA2, BRCA1, and RAD51 has also been analyzed. A deep neural network with a ‘Siamese Neural Network (SNN)’, architecture has been implemented using one-short learning process to comprehend the data and make valid predictions on TP53 mutation. This ‘algorithm and learning platform’ helps in making dependable predictions even from a low input data and the machine's measured predictive performance is 89%.
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从显微活检图像中早期预测P53突变致癌诊断系统的设计与开发
与癌症治疗相关的主要并发症是延迟癌症检测,这也会降低生存的可能性。这种情况可以通过早期诊断系统在一定程度上得到解决。在目前的研究中,利用“药物基因组学”、“基因表达谱”和“深度成像处理技术”,设计了TP53突变的早期检测系统,TP53突变是大多数癌症类型的常见原发突变。分析的输入是从“表达图谱数据库”收集的显微活检图像。在乳腺癌和卵巢癌样本中观察到TP53基因突变的高水平表达。相关基因如BARD1、CHEK2、ATM、BRCA2、BRCA1和RAD51的参与也被分析。一个具有“连体神经网络(SNN)”架构的深度神经网络已经实现,使用一个简短的学习过程来理解数据并对TP53突变做出有效的预测。这种“算法和学习平台”有助于从低输入数据中做出可靠的预测,机器的测量预测性能为89%。
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