DNA Microarray Expression Analysis and Data Mining for Blood Cancer

Dongguang Li
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引用次数: 7

Abstract

The paper systematically presents how to discover useful information based on the DNA microarray expression data collected from mouse experiments for the leukemia research. The BCR-ABL oncogene is the cause of Ph+ leukemia. The BCR gene, on chromosome 22, breaks either at exon 1, exon 12/13, or exon 19 and fuses to the c-ABL gene on chromosome 9 to form, respectively, three types of BCR-ABL chimerical gene: P190, P210, or P230. Each of the three forms of the BCR-ABL oncogene is associated with a distinct type of human leukemia. An introduction to knowledge discovery from microarray experimental datasets has been provided. Specifically, the fold change analysis is discussed, step by step, based on the microarray data obtained from the mouse experiments of P190, P210 and P230. Many soft computing methodologies, involving fuzzy sets, neural networks, genetic algorithms, rough sets, wavelets, and their hybridizations, have recently been suggested to provide approximate solutions at low cost, thereby speeding up the process.
血癌DNA微阵列表达分析与数据挖掘
本文系统地介绍了如何利用从小鼠实验中收集的DNA微阵列表达数据来发现白血病研究的有用信息。BCR-ABL癌基因是Ph+白血病的病因。22号染色体上的BCR基因在1号外显子、12/13外显子或19外显子断裂,并与9号染色体上的c-ABL基因融合,分别形成三种类型的BCR- abl嵌合基因:P190、P210和P230。三种形式的BCR-ABL癌基因中的每一种都与一种不同类型的人类白血病有关。介绍了从微阵列实验数据集发现知识的方法。具体而言,基于P190、P210和P230小鼠实验获得的微阵列数据,逐步讨论了折叠变化分析。许多软计算方法,包括模糊集、神经网络、遗传算法、粗糙集、小波及其杂交,最近被建议以低成本提供近似解,从而加快这一过程。
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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