A common-subsequence-based approach for mining deep order preserving submatrix

Yun Xue, TieChen Li, Zhiwen Liu, Zhengling Liao, Hua Xiao, Hongya Zhao, Xiaohui Hu
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引用次数: 2

Abstract

As an effective biclustering model, order-preserving submatrix (OPSM) has been widely applied to biological gene expression data mining. Recently, biologists hope to find deep OPSMs with long patterns and comparatively few support rows, which are not only useful on the interpretation of gene regulatory networks but also have essential biological significance. Unfortunately, the traditional exact mining algorithms based on Apriori principle could not deal with the deep OPSM problem, since they often take a large minimum support threshold for pattern pruning, and inevitably miss some significant deep OPSMs. Therefore, this paper proposes a new exact algorithm for mining deep OPSMs, which obtain all the deep OPSMs by finding the common subsequences shared by every two rows. Experiments have been done in both real and synthetic data sets, and the results show that our algorithm is suitable for the full mining of deep OPSMs with a small support, which could even find all the deep OPSMs with a minimum support threshold of 2. Compared with the traditional sequential pattern mining algorithms which depend on relatively large support threshold, our algorithm is an effective one to solve the deep OPSM problem.
基于公共子序列的深度保序子矩阵挖掘方法
作为一种有效的双聚类模型,保序子矩阵(OPSM)在生物基因表达数据挖掘中得到了广泛应用。近年来,生物学家希望找到具有较长模式和相对较少支持行的深层opsm,这不仅有助于解释基因调控网络,而且具有重要的生物学意义。然而,传统的基于Apriori原理的精确挖掘算法往往需要较大的最小支持阈值来进行模式修剪,难以处理深度OPSM问题,不可避免地会遗漏一些重要的深度OPSM。为此,本文提出了一种新的挖掘深度opsm的精确算法,该算法通过寻找每两行共享的公共子序列来获得所有深度opsm。在真实数据集和合成数据集上进行了实验,结果表明,该算法适用于小支持度深度opsm的全挖掘,甚至可以在最小支持度阈值为2的情况下找到所有深度opsm。与传统的依赖较大支持度阈值的顺序模式挖掘算法相比,该算法是解决深度OPSM问题的有效方法。
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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