scholarly journals A comparative study of biomarker gene selection methods in presence of outliers

2018 ◽  
Vol 25 ◽  
pp. 9-16
Author(s):  
M Shahjaman ◽  
N Kumar ◽  
AA Begum ◽  
SMS Islam ◽  
MNH Mollah
Keyword(s):  
Gene Expression ◽  
Data Analysis ◽  
Gene Expression Data ◽  
Gene Selection ◽  
Simulated Data ◽  
Small Sample ◽  
Data Sets ◽  
Expression Data ◽  
Selection Methods ◽  
Cancer Data

The main purpose of gene expression data analysis is to identify the biomarker genes by comparing the gene expression levels between two different groups or conditions. There are several methods to select biomarker genes and many comparative studies have been performed to select the appropriate method. However, they did not consider the problems of outliers in their data sets though it is very essential to select the method from robustness point of view due to outliers may occur in the different steps of the gene expression data generating process. In this paper, it is evaluated the performance among five popular statistical biomarker gene selection methods viz. T-test, SAM, LIMMA, KW and FCROS using both simulated and real gene expression data sets in absence and presence of outliers. In the simulated data analysis, it was demonstrated the performance of these methods in terms of different performance measures such as TPR, TNR, FPR, FNR and AUC and based on these measures, it was found that in absence of outliers, for both small-and-large sample cases all the methods perform almost similar. Whereas, in presence of outliers, for small-sample case only the FCROS method perform well than other methods. From a real colon cancer data analysis, it was elucidated that FCROS method identified additional 59 genes that were not detected by the other methods and most of them belongs to the different cancer related pathways.J. bio-sci. 25: 9-16, 2017

scholarly journals Incorporating Pathway Information into Feature Selection towards Better Performed Gene Signatures

2019 ◽  
Vol 2019 ◽  
pp. 1-12 ◽  
Author(s):  
Suyan Tian ◽  
Chi Wang ◽  
Bing Wang
Keyword(s):  
Gene Expression ◽  
Feature Selection ◽  
Gene Expression Data ◽  
Gene Selection ◽  
Selection Process ◽  
Biological Knowledge ◽  
Expression Data ◽  
Selection Methods ◽  
Its Gene ◽  
Active Research

To analyze gene expression data with sophisticated grouping structures and to extract hidden patterns from such data, feature selection is of critical importance. It is well known that genes do not function in isolation but rather work together within various metabolic, regulatory, and signaling pathways. If the biological knowledge contained within these pathways is taken into account, the resulting method is a pathway-based algorithm. Studies have demonstrated that a pathway-based method usually outperforms its gene-based counterpart in which no biological knowledge is considered. In this article, a pathway-based feature selection is firstly divided into three major categories, namely, pathway-level selection, bilevel selection, and pathway-guided gene selection. With bilevel selection methods being regarded as a special case of pathway-guided gene selection process, we discuss pathway-guided gene selection methods in detail and the importance of penalization in such methods. Last, we point out the potential utilizations of pathway-guided gene selection in one active research avenue, namely, to analyze longitudinal gene expression data. We believe this article provides valuable insights for computational biologists and biostatisticians so that they can make biology more computable.

CLASSIFYING TEMPORAL MICROARRAY DATA BY SELECTING INFORMATIVE GENES

2013 ◽  
Vol 11 (03) ◽  
pp. 1341006
Author(s):  
QIANG LOU ◽  
ZORAN OBRADOVIC
Keyword(s):  
Gene Expression ◽  
Feature Selection ◽  
Gene Expression Data ◽  
Microarray Data ◽  
Data Sets ◽  
Temporal Data ◽  
Expression Data ◽  
Selection Methods ◽  
Temporal Gene Expression ◽  
Single Matrix

In order to more accurately predict an individual's health status, in clinical applications it is often important to perform analysis of high-dimensional gene expression data that varies with time. A major challenge in predicting from such temporal microarray data is that the number of biomarkers used as features is typically much larger than the number of labeled subjects. One way to address this challenge is to perform feature selection as a preprocessing step and then apply a classification method on selected features. However, traditional feature selection methods cannot handle multivariate temporal data without applying techniques that flatten temporal data into a single matrix in advance. In this study, a feature selection filter that can directly select informative features from temporal gene expression data is proposed. In our approach, we measure the distance between multivariate temporal data from two subjects. Based on this distance, we define the objective function of temporal margin based feature selection to maximize each subject's temporal margin in its own relevant subspace. The experimental results on synthetic and two real flu data sets provide evidence that our method outperforms the alternatives, which flatten the temporal data in advance.

Methods for Gene Selection and Classification of Microarray Dataset

2018 ◽  
pp. 66-77
Author(s):  
Mekour Norreddine
Keyword(s):  
Gene Expression ◽  
Feature Selection ◽  
Gene Expression Data ◽  
Gene Selection ◽  
Information Gain ◽  
Microarray Dataset ◽  
Data Sets ◽  
Expression Data ◽  
Wrapper Approach ◽  
Filter Approach

One of the problems that gene expression data resolved is feature selection. There is an important process for choosing which features are important for prediction; there are two general approaches for feature selection: filter approach and wrapper approach. In this chapter, the authors combine the filter approach with method ranked information gain and wrapper approach with a searching method of the genetic algorithm. The authors evaluate their approach on two data sets of gene expression data: Leukemia, and the Central Nervous System. The classifier Decision tree (C4.5) is used for improving the classification performance.

Cancer Gene Expression Data Analysis Using Rough Based Symmetrical Clustering

2013 ◽  
pp. 1626-1641
Author(s):  
Anasua Sarkar ◽  
Ujjwal Maulik
Keyword(s):  
Gene Expression ◽  
Data Analysis ◽  
Gene Expression Data ◽  
Rough Set ◽  
Clustering Algorithm ◽  
Data Sets ◽  
Cancer Gene ◽  
Expression Data ◽  
Gene Expression Data Analysis ◽  
Cancer Subtypes

Identification of cancer subtypes is the central goal in the cancer gene expression data analysis. Modified symmetry-based clustering is an unsupervised learning technique for detecting symmetrical convex or non-convex shaped clusters. To enable fast automatic clustering of cancer tissues (samples), in this chapter, the authors propose a rough set based hybrid approach for modified symmetry-based clustering algorithm. A natural basis for analyzing gene expression data using the symmetry-based algorithm is to group together genes with similar symmetrical patterns of microarray expressions. Rough-set theory helps in faster convergence and initial automatic optimal classification, thereby solving the problem of unknown knowledge of number of clusters in gene expression measurement data. For rough-set-theoretic decision rule generation, each cluster is classified using heuristically searched optimal reducts to overcome overlapping cluster problem. The rough modified symmetry-based clustering algorithm is compared with another newly implemented rough-improved symmetry-based clustering algorithm and existing K-Means algorithm over five benchmark cancer gene expression data sets, to demonstrate its superiority in terms of validity. The statistical analyses are also performed to establish the significance of this rough modified symmetry-based clustering approach.

Cancer Gene Expression Data Analysis Using Rough Based Symmetrical Clustering

2013 ◽  
pp. 699-715 ◽  
Author(s):  
Anasua Sarkar ◽  
Ujjwal Maulik
Keyword(s):  
Gene Expression ◽  
Data Analysis ◽  
Gene Expression Data ◽  
Rough Set ◽  
Clustering Algorithm ◽  
Data Sets ◽  
Cancer Gene ◽  
Expression Data ◽  
Gene Expression Data Analysis ◽  
Cancer Subtypes

Identification of cancer subtypes is the central goal in the cancer gene expression data analysis. Modified symmetry-based clustering is an unsupervised learning technique for detecting symmetrical convex or non-convex shaped clusters. To enable fast automatic clustering of cancer tissues (samples), in this chapter, the authors propose a rough set based hybrid approach for modified symmetry-based clustering algorithm. A natural basis for analyzing gene expression data using the symmetry-based algorithm is to group together genes with similar symmetrical patterns of microarray expressions. Rough-set theory helps in faster convergence and initial automatic optimal classification, thereby solving the problem of unknown knowledge of number of clusters in gene expression measurement data. For rough-set-theoretic decision rule generation, each cluster is classified using heuristically searched optimal reducts to overcome overlapping cluster problem. The rough modified symmetry-based clustering algorithm is compared with another newly implemented rough-improved symmetry-based clustering algorithm and existing K-Means algorithm over five benchmark cancer gene expression data sets, to demonstrate its superiority in terms of validity. The statistical analyses are also performed to establish the significance of this rough modified symmetry-based clustering approach.

scholarly journals A COMPARATIVE STUDY ON GENE SELECTION METHODS FOR TISSUES CLASSIFICATION ON LARGE SCALE GENE EXPRESSION DATA

2016 ◽  
Vol 78 (5-10) ◽  
Author(s):  
Farzana Kabir Ahmad
Keyword(s):  
Gene Expression ◽  
Feature Selection ◽  
Gene Expression Data ◽  
Large Scale ◽  
Gene Selection ◽  
Support Vector ◽  
Breast Cancer Dataset ◽  
Expression Data ◽  
Selection Methods ◽  
Normal Tissues

Deoxyribonucleic acid (DNA) microarray technology is the recent invention that provided colossal opportunities to measure a large scale of gene expressions simultaneously. However, interpreting large scale of gene expression data remain a challenging issue due to their innate nature of “high dimensional low sample size”. Microarray data mainly involved thousands of genes, n in a very small size sample, p which complicates the data analysis process. For such a reason, feature selection methods also known as gene selection methods have become apparently need to select significant genes that present the maximum discriminative power between cancerous and normal tissues. Feature selection methods can be structured into three basic factions; a) filter methods; b) wrapper methods and c) embedded methods. Among these methods, filter gene selection methods provide easy way to calculate the informative genes and can simplify reduce the large scale microarray datasets. Although filter based gene selection techniques have been commonly used in analyzing microarray dataset, these techniques have been tested separately in different studies. Therefore, this study aims to investigate and compare the effectiveness of these four popular filter gene selection methods namely Signal-to-Noise ratio (SNR), Fisher Criterion (FC), Information Gain (IG) and t-Test in selecting informative genes that can distinguish cancer and normal tissues. In this experiment, common classifiers, Support Vector Machine (SVM) is used to train the selected genes. These gene selection methods are tested on three large scales of gene expression datasets, namely breast cancer dataset, colon dataset, and lung dataset. This study has discovered that IG and SNR are more suitable to be used with SVM. Furthermore, this study has shown SVM performance remained moderately unaffected unless a very small size of genes was selected.

scholarly journals Application of Biological Domain Knowledge Based Feature Selection on Gene Expression Data

Entropy ◽  
2020 ◽  
Vol 23 (1) ◽  
pp. 2
Author(s):  
Malik Yousef ◽  
Abhishek Kumar ◽  
Burcu Bakir-Gungor
Keyword(s):  
Gene Expression ◽  
Feature Selection ◽  
Data Analysis ◽  
Gene Expression Data ◽  
Gene Selection ◽  
Biological Data ◽  
Biological Information ◽  
Background Information ◽  
Biological Knowledge ◽  
Expression Data

In the last two decades, there have been massive advancements in high throughput technologies, which resulted in the exponential growth of public repositories of gene expression datasets for various phenotypes. It is possible to unravel biomarkers by comparing the gene expression levels under different conditions, such as disease vs. control, treated vs. not treated, drug A vs. drug B, etc. This problem refers to a well-studied problem in the machine learning domain, i.e., the feature selection problem. In biological data analysis, most of the computational feature selection methodologies were taken from other fields, without considering the nature of the biological data. Thus, integrative approaches that utilize the biological knowledge while performing feature selection are necessary for this kind of data. The main idea behind the integrative gene selection process is to generate a ranked list of genes considering both the statistical metrics that are applied to the gene expression data, and the biological background information which is provided as external datasets. One of the main goals of this review is to explore the existing methods that integrate different types of information in order to improve the identification of the biomolecular signatures of diseases and the discovery of new potential targets for treatment. These integrative approaches are expected to aid the prediction, diagnosis, and treatment of diseases, as well as to enlighten us on disease state dynamics, mechanisms of their onset and progression. The integration of various types of biological information will necessitate the development of novel techniques for integration and data analysis. Another aim of this review is to boost the bioinformatics community to develop new approaches for searching and determining significant groups/clusters of features based on one or more biological grouping functions.

scholarly journals Application of Biological Domain Knowledge Based Feature Selection on Gene Expression Data

2020 ◽  
Author(s):  
Malik Yousef ◽  
Abhishek Kumar ◽  
Burcu Bakir-Gungor
Keyword(s):  
Gene Expression ◽  
Feature Selection ◽  
Data Analysis ◽  
Gene Expression Data ◽  
Gene Selection ◽  
Selection Process ◽  
Biological Data ◽  
Integrative Approach ◽  
Biological Knowledge ◽  
Expression Data

In the last two decades, there have been massive advancements in high throughput technologies, which resulted in the exponential growth of public repositories of gene expression datasets for various phenotypes. It is possible to unravel biomarkers by comparing the gene expression levels under different conditions, such as disease vs. control, treated vs. not treated, drug A vs. drug B, etc. This problem refers to a well-studied problem in the machine learning domain, i.e., the feature selection problem. In biological data analysis, most of the computational feature selection methodologies were taken from other fields, without considering the nature of the biological data. For gene expression data analysis, most of the existing feature selection methods rely on expression values alone to select the genes; and biological knowledge is integrated at the end of the analysis in order to gain biological insights or to support the initial findings. Thus, integrative approaches that utilize the biological knowledge while performing feature selection are necessary for this kind of data. The main idea behind the integrative gene selection process is to generate a ranked list of genes considering both the statistical metrics that are applied to the gene expression data, and the biological background information which is provided as external datasets. Since the integrative approach attracted attention in the gene expression domain, lately the gene selection process shifted from being purely data-centric to more incorporative analysis with additional biological knowledge.

scholarly journals Case-Based Retrieval Framework for Gene Expression Data

2015 ◽  
Vol 14 ◽  
pp. CIN.S22371 ◽  
Author(s):  
Ali Anaissi ◽  
Madhu Goyal ◽  
Daniel R. Catchpoole ◽  
Ali Braytee ◽  
Paul J. Kennedy
Keyword(s):  
Gene Expression ◽  
Prostate Cancer ◽  
Gene Expression Data ◽  
Childhood Leukemia ◽  
Data Sets ◽  
Expression Data ◽  
Data Set ◽  
Cancer Data ◽  
Leukemia Data ◽  
Case Based

Background The process of retrieving similar cases in a case-based reasoning system is considered a big challenge for gene expression data sets. The huge number of gene expression values generated by microarray technology leads to complex data sets and similarity measures for high-dimensional data are problematic. Hence, gene expression similarity measurements require numerous machine-learning and data-mining techniques, such as feature selection and dimensionality reduction, to be incorporated into the retrieval process. Methods This article proposes a case-based retrieval framework that uses a k-nearest-neighbor classifier with a weighted-feature-based similarity to retrieve previously treated patients based on their gene expression profiles. Results The herein-proposed methodology is validated on several data sets: a childhood leukemia data set collected from The Children's Hospital at Westmead, as well as the Colon cancer, the National Cancer Institute (NCI), and the Prostate cancer data sets. Results obtained by the proposed framework in retrieving patients of the data sets who are similar to new patients are as follows: 96% accuracy on the childhood leukemia data set, 95% on the NCI data set, 93% on the Colon cancer data set, and 98% on the Prostate cancer data set. Conclusion The designed case-based retrieval framework is an appropriate choice for retrieving previous patients who are similar to a new patient, on the basis of their gene expression data, for better diagnosis and treatment of childhood leukemia. Moreover, this framework can be applied to other gene expression data sets using some or all of its steps.

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