关于微阵列数据的归一化、变量选择、分类或聚类的论文

David M. Rocke, T. Ideker, O. Troyanskaya, John Quackenbush, J. Dopazo
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引用次数: 58

摘要

在过去的十年左右,已经发表了大量关于微阵列数据规范化、变量(基因)选择、分类和聚类的方法。正如生物信息学的范围文件所指出的,这要求描述这些问题的新方法的论文达到非常高的标准,显示出对真实生物数据的结果的重要改进,以及新颖性。在这篇社论中,我们描述了一些需要满足的标准,这些领域的论文被认真考虑。我们要求未来的作者在将论文提交给生物信息学之前仔细考虑这些要点。模拟的作用。模拟在研究各种数据分析方法的特性时是有用的。然而,在微阵列研究中可靠地使用模拟存在重要障碍,这主要是由于我们不知道测量基因表达水平的统计分布。首先,真实表达值的转录本分布取决于组织或细胞的生物学状态,对于给定的状态,这是未知的,即使以分布形式,也可能进一步表现出基因特异性和平台特异性效应。其次,真实表达的生物复制内部的相关性是未知的,并且很可能是不可知的细节,因为它是
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Papers on normalization, variable selection, classification or clustering of microarray data
Over the last decade or so, there have been large numbers of methods published on approaches for normalization, variable (gene) selection, classification, and clustering of microarray data. As indicated in the scope document for Bioinformatics, this requires papers describing new methods for these problems to meet a very high standard, showing important improvement in results for real biological data, as well as novelty. In this editorial, we describe some standards that need to be met for papers in these areas to be seriously considered. We ask that prospective authors consider these points carefully before submission of their papers to Bioinformatics. The Role of Simulation. Simulation can be useful in investigating the properties of various methods of data analysis. Yet there are important barriers to credible use of simulation in microarray studies, largely due to what we don’t know about the statistical distribution of measured gene expression levels. First, the distribution across transcripts of true expression values is dependent on the biological state of the tissue or cell, and for a given state this is unknown, even in distributional form, and may further exhibit genespecific and platform-specific effects. Second, the correlation within biological replicates of true expression is unknown, and is likely unknowable in detail given that it is
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