An advanced omic approach to identify co-regulated clusters and transcription regulation network with AGCT and SHOE methods

Natalia Polouliakh*, Richard Nock

*Corresponding author for this work

    Research output: Chapter in Book/Report/Conference proceedingChapterpeer-review

    Abstract

    To obtain the global picture of genetic machinery for massive high-throughput gene expression data, novel data-driven unsupervised learning approaches are becoming essentially important. For this purpose, basic analytic workflow has been established and should include two steps: first, unsupervised clustering to identify genes with similar behavior upon exposure to a signal, and second, identification of transcription factors regulating those genes. In this chapter, we will describe an advanced tool that can be used for analyzing and characterizing large-scale time-series gene expression composed of a two-step approach. For the first step, we developed an original method “A Geometric Clustering Tool” (AGCT) that unveils the complex architecture of large-scale time-series gene expression data in a real-time manner using cutting edge techniques of low dimension manifold learning, data clustering, and visualization. For the second step, we established an original method “Sequence Homology in Eukaryotes” (SHOE) executing comparative genomic analysis on humans, mice, and rats.

    Original languageEnglish
    Title of host publicationMethods in Molecular Biology
    PublisherHumana Press Inc.
    Pages373-389
    Number of pages17
    DOIs
    Publication statusPublished - 2017

    Publication series

    NameMethods in Molecular Biology
    Volume1598
    ISSN (Print)1064-3745

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