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基于微阵列数据的基因网络预测方法研究进展
引用本文:王明怡,夏顺仁,陈作舟.基于微阵列数据的基因网络预测方法研究进展[J].生物物理学报,2005,21(1):19-25.
作者姓名:王明怡  夏顺仁  陈作舟
作者单位:1. 浙江大学生命科学学院,杭州,310029;中国计量学院计算机科学与工程学系,杭州,310018
2. 浙江大学CAD&CG国家重点实验室,杭州,310027;浙江大学生物医学工程教育部重点实验室,杭州,310027
3. 浙江大学生命科学学院,杭州,310029
基金项目:国家自然科学基金资助课题(60272029),浙江省自然科学基金资助课题(M603227)
摘    要:DNA微阵列技术可同时定量测定成千上万个基因在生物样本中的表达水平,从这一技术获得的全基因组范围表达数据为揭示基因间复杂调控关系提供了可能。研究人员试图通过数学和计算方法来构建遗传互作的模型,这些基因调控网络模型有聚类法、布尔网络、贝叶斯网络、微分方程等。文章对网络重建计算方法的研究现状进行了较为全面的综述,比较了不同模型的优缺点,并对该领域进一步的研究趋势进行了展望。

关 键 词:基因网络  微阵列  聚类  布尔网络  微分方程  贝叶斯网络
收稿时间:2004-10-21
修稿时间:2004年10月21

Progress on methods for inferring the gene networks from microarray data
WANG Ming-yi,XIA Shun-ren,CHEN Zuo-zhou.Progress on methods for inferring the gene networks from microarray data[J].Acta Biophysica Sinica,2005,21(1):19-25.
Authors:WANG Ming-yi  XIA Shun-ren  CHEN Zuo-zhou
Institution:1. College of Life Science, Zhejiang University, Hangzhou 310029|China|
2. Department of Computer Science and Engineering, China Jiliang University, Hangzhou 310018, China|
3. State Key Lab of CAD &|CG, Zhejiang University, Hangzhou 310027, China|
4. Key Laboratory of Biomedical Engineering of Ministry of Education, Zhejiang University, Hangzhou 310027, China
Abstract:DNA microarray technology makes it feasible to obtain quantitative measurements of expression of thousands of genes that present in a biological sample simultaneously. Genome-wide expression data generated from this technology are promising to uncover the complex relationships between these genes. Mathematical and computational methods are being developed in order to construct formal models of genetic interactions. There have been a number of attempts to model gene regulatory networks, including clustering, Boolean networks, Bayesian networks and differential equations. The present situation in computerized gene network reconstruction techniques was reviewed in detail. The specific advantages and disadvantages of these models were explained. Moreover, some valuable issues for future exploration in this area were indicated and discussed.
Keywords:Gene networks  Microarrays  Clustering  Boolean networks  Differential equations  Bayesian networks
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