Please use this identifier to cite or link to this item: https://doi.org/10.3389/fgene.2018.00194
Title: Matrix Integrative Analysis (MIA) of multiple genomic data for modular patterns
Authors: Chen, J 
Zhang, S
Keywords: microRNA
Article
bioinformatics
biology
copy number variation
DNA methylation
drug targeting
gene expression
gene interaction
gene regulatory network
genome analysis
human
mathematical analysis
matrix integrative analysis
principal component analysis
simulation
tumor classification
validation study
Issue Date: 2018
Citation: Chen, J, Zhang, S (2018). Matrix Integrative Analysis (MIA) of multiple genomic data for modular patterns. Frontiers in Genetics 9 (MAY) : 194. ScholarBank@NUS Repository. https://doi.org/10.3389/fgene.2018.00194
Rights: Attribution 4.0 International
Abstract: The increasing availability of high-throughput biological data, especially multi-dimensional genomic data across the same samples, has created an urgent need for modular and integrative analysis tools that can reveal the relationships among different layers of cellular activities. To this end, we present a MATLAB package, Matrix Integration Analysis (MIA), implementing and extending four published methods, designed based on two classical techniques, non-negative matrix factorization (NMF), and partial least squares (PLS). This package can integrate diverse types of genomic data (e.g., copy number variation, DNA methylation, gene expression, microRNA expression profiles, and/or gene network data) to identify the underlying modular patterns by each method. Particularly, we demonstrate the differences between these two classes of methods, which give users some suggestions about how to select a suitable method in the MIA package. MIA is a flexible tool which could handle a wide range of biological problems and data types. Besides, we also provide an executable version for users without a MATLAB license. © 2018 Chen and Zhang.
Source Title: Frontiers in Genetics
URI: https://scholarbank.nus.edu.sg/handle/10635/178089
ISSN: 16648021
DOI: 10.3389/fgene.2018.00194
Rights: Attribution 4.0 International
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