“Who are the key players behind a disease state?”: Outcomes of a new computational approach on cancer data

Jeethu V. Devasia, P. Chandran
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引用次数: 1

Abstract

The problem of identifying disease causing genes and dysregulated pathways has attained a key position in computational biology research, as it helps in understanding major causal genes and their interactions behind a disease state and thereby enables proposing new drug targets. The development of computational approaches for the inference of disease causing genes and associated pathways can improve the accuracy and efficiency and reduce the cost of biomedical analysis. Identification of disease causing genes from the large set of genes produced by high throughput experiments is a time consuming and costly process. Based on the fact that interactions among several genes results in certain phenotypes, the molecular interaction network is a major resource for computational approaches to identify disease causing genes and associated pathways. Executing computations on the huge molecular interaction network is also major challenge. Here, we address the problem of inferring disease causing genes and their pathways using graph theoretical approaches which focus on reducing the execution time by using graph pruning techniques, without compromising on accuracy of results. Experimentation on real biological data shows reduced execution time and increased accuracy than other methods reported in literature on benchmark datasets, on using the proposed technique.
“谁是疾病状态背后的关键人物?”:癌症数据新计算方法的结果
识别致病基因和失调通路的问题在计算生物学研究中占据了关键地位,因为它有助于理解疾病状态背后的主要致病基因及其相互作用,从而能够提出新的药物靶点。用于推断致病基因和相关途径的计算方法的发展可以提高生物医学分析的准确性和效率,并降低成本。从高通量实验产生的大量基因中鉴定致病基因是一个耗时且昂贵的过程。基于几个基因之间的相互作用导致某些表型的事实,分子相互作用网络是识别致病基因和相关途径的计算方法的主要资源。在巨大的分子相互作用网络上执行计算也是一个重大挑战。在这里,我们使用图论方法解决了推断致病基因及其途径的问题,图论方法侧重于通过使用图修剪技术减少执行时间,同时不影响结果的准确性。在真实生物数据上的实验表明,与文献中在基准数据集上报道的其他方法相比,使用所提出的技术可以减少执行时间,提高准确性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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