5,483 research outputs found
Elephant Search with Deep Learning for Microarray Data Analysis
Even though there is a plethora of research in Microarray gene expression
data analysis, still, it poses challenges for researchers to effectively and
efficiently analyze the large yet complex expression of genes. The feature
(gene) selection method is of paramount importance for understanding the
differences in biological and non-biological variation between samples. In
order to address this problem, a novel elephant search (ES) based optimization
is proposed to select best gene expressions from the large volume of microarray
data. Further, a promising machine learning method is envisioned to leverage
such high dimensional and complex microarray dataset for extracting hidden
patterns inside to make a meaningful prediction and most accurate
classification. In particular, stochastic gradient descent based Deep learning
(DL) with softmax activation function is then used on the reduced features
(genes) for better classification of different samples according to their gene
expression levels. The experiments are carried out on nine most popular Cancer
microarray gene selection datasets, obtained from UCI machine learning
repository. The empirical results obtained by the proposed elephant search
based deep learning (ESDL) approach are compared with most recent published
article for its suitability in future Bioinformatics research.Comment: 12 pages, 5 Tabl
Feature Selection via Binary Simultaneous Perturbation Stochastic Approximation
Feature selection (FS) has become an indispensable task in dealing with
today's highly complex pattern recognition problems with massive number of
features. In this study, we propose a new wrapper approach for FS based on
binary simultaneous perturbation stochastic approximation (BSPSA). This
pseudo-gradient descent stochastic algorithm starts with an initial feature
vector and moves toward the optimal feature vector via successive iterations.
In each iteration, the current feature vector's individual components are
perturbed simultaneously by random offsets from a qualified probability
distribution. We present computational experiments on datasets with numbers of
features ranging from a few dozens to thousands using three widely-used
classifiers as wrappers: nearest neighbor, decision tree, and linear support
vector machine. We compare our methodology against the full set of features as
well as a binary genetic algorithm and sequential FS methods using
cross-validated classification error rate and AUC as the performance criteria.
Our results indicate that features selected by BSPSA compare favorably to
alternative methods in general and BSPSA can yield superior feature sets for
datasets with tens of thousands of features by examining an extremely small
fraction of the solution space. We are not aware of any other wrapper FS
methods that are computationally feasible with good convergence properties for
such large datasets.Comment: This is the Istanbul Sehir University Technical Report
#SHR-ISE-2016.01. A short version of this report has been accepted for
publication at Pattern Recognition Letter
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The robust selection of predictive genes via a simple classifier
Identifying genes that direct the mechanism of a disease from expression data is extremely useful in understanding how that mechanism works.
This in turn may lead to better diagnoses and potentially can lead to a cure for that disease. This task becomes extremely challenging when the
data are characterised by only a small number of samples and a high number of dimensions, as it is often the case with gene expression data.
Motivated by this challenge, we present a general framework that focuses on simplicity and data perturbation. These are the keys for the robust
identification of the most predictive features in such data. Within this framework, we propose a simple selective naĀØıve Bayes classifier discovered using a global search technique, and combine it with data perturbation to
increase its robustness to small sample sizes.
An extensive validation of the method was carried out using two applied datasets from the field of microarrays and a simulated dataset, all
confounded by small sample sizes and high dimensionality. The method has been shown capable of identifying genes previously confirmed or associated with prostate cancer and viral infections
Feature selection for microarray gene expression data using simulated annealing guided by the multivariate joint entropy
In this work a new way to calculate the multivariate joint entropy is presented. This measure is the basis for a fast information-theoretic based evaluation of gene relevance in a Microarray Gene Expression data context. Its low complexity is based on the reuse of previous computations to calculate current feature relevance. The mu-TAFS algorithm --named as such to differentiate it from previous TAFS algorithms-- implements a simulated annealing technique specially designed for feature subset selection. The algorithm is applied to the maximization of gene subset relevance in several public-domain microarray data sets. The experimental results show a notoriously high classification performance and low size subsets formed by biologically meaningful genes.Postprint (published version
Techniques for clustering gene expression data
Many clustering techniques have been proposed for the analysis of gene expression data obtained from microarray experiments. However, choice of suitable method(s) for a given experimental dataset is not straightforward. Common approaches do not translate well and fail to take account of the data profile. This review paper surveys state of the art applications which recognises these limitations and implements procedures to overcome them. It provides a framework for the evaluation of clustering in gene expression analyses. The nature of microarray data is discussed briefly. Selected examples are presented for the clustering methods considered
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Temporal Bayesian classifiers for modelling muscular dystrophy expression data
The analysis of microarray data from time-series experiments requires specialised algorithms, which take the temporal ordering of the data into account. In this paper we explore a new architecture of Bayesian classifier that can be used to understand how biological mechanisms differ with respect to time. We show that this classifier improves the classification of microarray data and at the same time ensures that the models can easily be analysed by biologists by incorporating time transparently. In this paper we focus on data that has been generated to explore different types of muscular dystrophy
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