48,501 research outputs found

    Discriminative Gene Selection Employing Linear Regression Model

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    Microarray datasets enables the analysis of expression of thousands of genes across hundreds of samples. Usually classifiers do not perform well for large number of features (genes) as is the case of microarray datasets. That is why a small number of informative and discriminative features are always desirable for efficient classification. Many existing feature selection approaches have been proposed which attempts sample classification based on the analysis of gene expression values. In this paper a linear regression based feature selection algorithm for two class microarray datasets has been developed which divides the training dataset into two subtypes based on the class information. Using one of the classes as the base condition, a linear regression based model is developed. Using this regression model the divergence of each gene across the two classes are calculated and thus genes with higher divergence values are selected as important features from the second subtype of the training data. The classification performance of the proposed approach is evaluated with SVM, Random Forest and AdaBoost classifiers. Results show that the proposed approach provides better accuracy values compared to other existing approaches i.e. ReliefF, CFS, decision tree based attribute selector and attribute selection using correlation analysis

    Multi-test Decision Tree and its Application to Microarray Data Classification

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    Objective: The desirable property of tools used to investigate biological data is easy to understand models and predictive decisions. Decision trees are particularly promising in this regard due to their comprehensible nature that resembles the hierarchical process of human decision making. However, existing algorithms for learning decision trees have tendency to underfit gene expression data. The main aim of this work is to improve the performance and stability of decision trees with only a small increase in their complexity. Methods: We propose a multi-test decision tree (MTDT); our main contribution is the application of several univariate tests in each non-terminal node of the decision tree. We also search for alternative, lower-ranked features in order to obtain more stable and reliable predictions. Results: Experimental validation was performed on several real-life gene expression datasets. Comparison results with eight classifiers show that MTDT has a statistically significantly higher accuracy than popular decision tree classifiers, and it was highly competitive with ensemble learning algorithms. The proposed solution managed to outperform its baseline algorithm on 1414 datasets by an average 66 percent. A study performed on one of the datasets showed that the discovered genes used in the MTDT classification model are supported by biological evidence in the literature. Conclusion: This paper introduces a new type of decision tree which is more suitable for solving biological problems. MTDTs are relatively easy to analyze and much more powerful in modeling high dimensional microarray data than their popular counterparts

    An efficient randomised sphere cover classifier

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    This paper describes an efficient randomised sphere cover classifier(aRSC), that reduces the training data set size without loss of accuracy when compared to nearest neighbour classifiers. The motivation for developing this algorithm is the desire to have a non-deterministic, fast, instance-based classifier that performs well in isolation but is also ideal for use with ensembles. We use 24 benchmark datasets from UCI repository and six gene expression datasets for evaluation. The first set of experiments demonstrate the basic benefits of sphere covering. The second set of experiments demonstrate that when we set the a parameter through cross validation, the resulting aRSC algorithm outperforms several well known classifiers when compared using the Friedman rank sum test. Thirdly, we test the usefulness of aRSC when used with three feature filtering filters on six gene expression datasets. Finally, we highlight the benefits of pruning with a bias/variance decompositio

    Factorised Representations of Query Results

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    Query tractability has been traditionally defined as a function of input database and query sizes, or of both input and output sizes, where the query result is represented as a bag of tuples. In this report, we introduce a framework that allows to investigate tractability beyond this setting. The key insight is that, although the cardinality of a query result can be exponential, its structure can be very regular and thus factorisable into a nested representation whose size is only polynomial in the size of both the input database and query. For a given query result, there may be several equivalent representations, and we quantify the regularity of the result by its readability, which is the minimum over all its representations of the maximum number of occurrences of any tuple in that representation. We give a characterisation of select-project-join queries based on the bounds on readability of their results for any input database. We complement it with an algorithm that can find asymptotically optimal upper bounds and corresponding factorised representations.Comment: 44 pages, 13 figure
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