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Identification of Genetic Pathway for Cervical Cancer Development Using Rough and Bayesian Theory

机译:应用粗糙和贝叶斯理论确定宫颈癌发展的遗传途径

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Suitable analysis of microarray dataset can unlock the mystery of the origin of many dreaded disease like cancer which can subsequently be investigated for its rectification, resulting into search for drug design. A critical challenge of the post-genomic era is to find out the cancer causing genes that induce changes in gene expression profiles in the microarray dataset. Various algorithms based on SVM, Data Mining Techniques, Information theory based investigations, Clustering Techniques etc. were used by previous researchers. In this paper, Rough Set Theory and Bayesian Network based techniques have been applied for the same purpose. Rough Set has been used to isolate genes from microarray dataset responsible for cervical cancer. Bayesian approach has been used for extracting the Gene Regulating Network using the isolated genes. The same has been repeated for a normal healthy person. By superimposing these two networks, it is possible to find out the distinct cellular pathway for development of cancer from the departure of directed edges of the two networks. The results obtained in this work are quite satisfactory.
机译:对微阵列数据集进行适当的分析可以揭开许多可怕疾病(如癌症)起源的谜团,随后可以对其进行纠正以进行研究,从而寻求药物设计。后基因组时代的一个关键挑战是找出引起癌症的基因,这些基因会诱导微阵列数据集中基因表达谱的变化。以前的研究人员使用了基于支持向量机,数据挖掘技术,基于信息论的研究,聚类技术等各种算法。在本文中,基于相同目的的粗糙集理论和基于贝叶斯网络的技术已被应用。粗糙集已用于从负责宫颈癌的微阵列数据集中分离基因。贝叶斯方法已用于使用分离的基因提取基因调控网络。对于正常健康的人,已经重复了同样的事情。通过叠加这两个网络,有可能从两个网络的有向边缘的偏离中找出癌症发展的独特细胞途径。在这项工作中获得的结果是令人满意的。

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