基于配置文件的字符串核远程同源性检测和基序提取。

Rui Kuang, Eugene Ie, Ke Wang, Kai Wang, Mahira Siddiqi, Yoav Freund, Christina Leslie
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引用次数: 0

摘要

我们引入了新的基于谱的字符串核,用于支持向量机(svm)的蛋白质分类和远程同源性检测问题。这些核使用概率谱,例如由PSI-BLAST算法产生的概率谱,来定义蛋白质序列上的位置依赖突变邻域,以实现数据中k-长度子序列(“k-mers”)的不精确匹配。通过使用高效的数据结构,一旦获得轮廓,就可以快速计算出核。例如,运行PSI-BLAST以构建pro- files所需的时间明显长于内核计算时间和SVM训练时间。我们提出了基于SCOP数据库的远程同源检测实验,在实验中,我们表明基于配置文件的字符串核与支持向量机分类器一起使用,远远优于最近提出的所有监督支持向量机方法。我们还展示了如何使用学习到的SVM分类器来提取“判别序列基序”(discriminative sequence motifs)——原始剖面的短区域几乎贡献了SVM分类得分的所有权重——并表明这些判别基序对应于蛋白质数据中有意义的结构特征。PSI-BLAST配置文件的使用可以看作是一种半监督学习技术,因为PSI-BLAST利用来自大型序列数据库的未标记数据来构建更多信息的配置文件。最近提出的“聚类核”给出了提高支持向量机蛋白质分类性能的一般半监督方法。我们展示了我们的概要内核结果与集群内核相当,同时为大型数据集提供了更好的可伸缩性。
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Profile-based string kernels for remote homology detection and motif extraction.

We introduce novel profile-based string kernels for use with support vector machines (SVMs) for the problems of protein classification and remote homology detection. These kernels use probabilistic profiles, such as those produced by the PSI-BLAST algorithm, to define position-dependent mutation neighborhoods along protein sequences for inexact matching of k-length subsequences ("k-mers") in the data. By use of an efficient data structure, the kernels are fast to compute once the profiles have been obtained. For example, the time needed to run PSI-BLAST in order to build the pro- files is significantly longer than both the kernel computation time and the SVM training time. We present remote homology detection experiments based on the SCOP database where we show that profile-based string kernels used with SVM classifiers strongly outperform all recently presented supervised SVM methods. We also show how we can use the learned SVM classifier to extract "discriminative sequence motifs" -- short regions of the original profile that contribute almost all the weight of the SVM classification score -- and show that these discriminative motifs correspond to meaningful structural features in the protein data. The use of PSI-BLAST profiles can be seen as a semi-supervised learning technique, since PSI-BLAST leverages unlabeled data from a large sequence database to build more informative profiles. Recently presented "cluster kernels" give general semi-supervised methods for improving SVM protein classification performance. We show that our profile kernel results are comparable to cluster kernels while providing much better scalability to large datasets.

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Tree decomposition based fast search of RNA structures including pseudoknots in genomes. An algebraic geometry approach to protein structure determination from NMR data. A tree-decomposition approach to protein structure prediction. A pivoting algorithm for metabolic networks in the presence of thermodynamic constraints. A topological measurement for weighted protein interaction network.
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