Please use this identifier to cite or link to this item: https://doi.org/10.3389/fgene.2018.00194
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dc.titleMatrix Integrative Analysis (MIA) of multiple genomic data for modular patterns
dc.contributor.authorChen, J
dc.contributor.authorZhang, S
dc.date.accessioned2020-10-20T05:03:52Z
dc.date.available2020-10-20T05:03:52Z
dc.date.issued2018
dc.identifier.citationChen, 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
dc.identifier.issn16648021
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/178089
dc.description.abstractThe 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.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectmicroRNA
dc.subjectArticle
dc.subjectbioinformatics
dc.subjectbiology
dc.subjectcopy number variation
dc.subjectDNA methylation
dc.subjectdrug targeting
dc.subjectgene expression
dc.subjectgene interaction
dc.subjectgene regulatory network
dc.subjectgenome analysis
dc.subjecthuman
dc.subjectmathematical analysis
dc.subjectmatrix integrative analysis
dc.subjectprincipal component analysis
dc.subjectsimulation
dc.subjecttumor classification
dc.subjectvalidation study
dc.typeArticle
dc.contributor.departmentMATHEMATICS
dc.description.doi10.3389/fgene.2018.00194
dc.description.sourcetitleFrontiers in Genetics
dc.description.volume9
dc.description.issueMAY
dc.description.page194
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