ArticleBioMed research international2015
Multiblock discriminant analysis for integrative genomic study.
Article in BioMed research international, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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Who cites it
4 citing papers in PubMed.
- A roadmap for multi-omics data integration using deep learning.Briefings in bioinformatics · 2022Review
- Multi-block Analysis of Genomic Data Using Generalized Canonical Correlation Analysis.Genomics & informatics · 2018Article
- Genomic analyses of African Trypanozoon strains to assess evolutionary relationships and identify markers for strain identification.PLoS neglected tropical diseases · 2017Article
- Integration of multi-omics data for integrative gene regulatory network inference.International journal of data mining and bioinformaticsArticle
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Authors and funding
4 authors.
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Abstract
Human diseases are abnormal medical conditions in which multiple biological components are complicatedly involved. Nevertheless, most contributions of research have been made with a single type of genetic data such as Single Nucleotide Polymorphism (SNP) or Copy Number Variation (CNV). Furthermore, epigenetic modifications and transcriptional regulations have to be considered to fully exploit the knowledge of the complex human diseases as well as the genomic variants. We call the collection of the multiple heterogeneous data "multiblock data." In this paper, we propose a novel Multiblock Discriminant Analysis (MultiDA) method that provides a new integrative genomic model for the multiblock analysis and an efficient algorithm for discriminant analysis. The integrative genomic model is built by exploiting the representative genomic data including SNP, CNV, DNA methylation, and gene expression. The efficient algorithm for the discriminant analysis identifies discriminative factors of the multiblock data. The discriminant analysis is essential to discover biomarkers in computational biology. The performance of the proposed MultiDA was assessed by intensive simulation experiments, where the outstanding performance comparing the related methods was reported. As a target application, we applied MultiDA to human brain data of psychiatric disorders. The findings and gene regulatory network derived from the experiment are discussed.
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