从微阵列数据推断基因调控网络:一种模糊逻辑方法

P.C.H. Ma, Keith C. C. Chan
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引用次数: 1

摘要

最近在基因表达的大规模监测方面的发展,如DNA微阵列,使得基因调控网络(grn)的重建成为可能。在可以推断这些网络的结构之前,重要的是要确定,对于网络中的每个基因,哪些基因可以影响其表达以及它们如何影响它。大多数现有的方法都是有用的探索性工具,因为它们允许用户产生关于基因转录调控的生物学假设,然后可以在实验室中进行测试。然而,通过这些方法发现的模式并不足以在新的或持续的实验中对基因表达模式做出准确的预测。因此,很难比较不同方法的性能或决定哪种方法可能产生合理的假设。因此,我们需要一种方法,不仅可以提供对grn结构的可解释的见解,而且可以提供准确的预测。在本文中,我们提出了一种新的基于模糊逻辑的方法来解决这个问题。本文算法的期望特性如下:(i)它能够直接挖掘高维表达数据,而不需要额外的特征选择程序,(ii)它能够在预测预测基因的表达模式时区分相关和不相关的表达数据,(iii)基于提出的客观兴趣度测量,不需要预先指定用户阈值,(iv)它可以为可能的生物学解释发现明确的隐藏模式。(v)发现的模式可用于预测其他看不见的组织样本中的基因表达模式,并且(vi)使用模糊逻辑,它对表达数据中的噪声具有鲁棒性,因为它隐藏了定量属性相邻间隔的边界。基于真实表达数据的实验结果表明,该方法非常有效,所发现的模式揭示了具有生物学意义的基因调控关系,可以帮助用户重建grn的底层结构。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inference of Gene Regulatory Networks from Microarray Data: A Fuzzy Logic Approach
Recent developments in large-scale monitoring of gene expression such as DNA microarrays have made the reconstruction of gene regulatory networks (GRNs) feasible. Before one can infer the structures of these networks, it is important to identify, for each gene in the network, which genes can affect its expression and how they affect it. Most of the existing approaches are useful exploratory tools in the sense that they allow the user to generate biological hypotheses about transcriptional regulations of genes that can then be tested in the laboratory. However, the patterns discovered by these approaches are not adequate for making accurate prediction on gene expression patterns in new or held-out experiments. Therefore, it is difficult to compare performance of different approaches or decide which approach is likely to generate plausible hypothesis. For this reason, we need an approach that not only can provide interpretable insight into the structures of GRNs but also can provide accurate prediction. In this paper, we present a novel fuzzy logic-based approach for this problem. The desired characteristics of the proposed algorithm are as follows: (i) it is able to directly mine the high-dimensional expression data without the need for additional feature selection procedures, (ii) it is able to distinguish between relevant and irrelevant expression data in predicting the expression patterns of predicted genes, (iii) based on the proposed objective interestingness measure, no user-specified thresholds are needed in advance, (iv) it can make explicit hidden patterns discovered for possible biological interpretation, (v) the discovered patterns can be used to predict gene expression patterns in other unseen tissue samples, and (vi) with fuzzy logic, it is robust to noise in the expression data as it hides the boundaries of the adjacent intervals of the quantitative attributes. Experimental results on real expression data show that it can be very effective and the discovered patterns reveal biologically meaningful regulatory relationships of genes that could help the user reconstructing the underlying structures of GRNs.
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