Literature DB >> 29028263

Epigenomic annotation-based interpretation of genomic data: from enrichment analysis to machine learning.

Mikhail G Dozmorov1.   

Abstract

MOTIVATION: One of the goals of functional genomics is to understand the regulatory implications of experimentally obtained genomic regions of interest (ROIs). Most sequencing technologies now generate ROIs distributed across the whole genome. The interpretation of these genome-wide ROIs represents a challenge as the majority of them lie outside of functionally well-defined protein coding regions. Recent efforts by the members of the International Human Epigenome Consortium have generated volumes of functional/regulatory data (reference epigenomic datasets), effectively annotating the genome with epigenomic properties. Consequently, a wide variety of computational tools has been developed utilizing these epigenomic datasets for the interpretation of genomic data.
RESULTS: The purpose of this review is to provide a structured overview of practical solutions for the interpretation of ROIs with the help of epigenomic data. Starting with epigenomic enrichment analysis, we discuss leading tools and machine learning methods utilizing epigenomic and 3D genome structure data. The hierarchy of tools and methods reviewed here presents a practical guide for the interpretation of genome-wide ROIs within an epigenomic context. CONTACT: mikhail.dozmorov@vcuhealth.org. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
© The Author 2017. Published by Oxford University Press. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com

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Mesh:

Year:  2017        PMID: 29028263     DOI: 10.1093/bioinformatics/btx414

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


  12 in total

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3.  Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program.

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Journal:  Genome Med       Date:  2021-08-26       Impact factor: 15.266

4.  BART: a transcription factor prediction tool with query gene sets or epigenomic profiles.

Authors:  Zhenjia Wang; Mete Civelek; Clint L Miller; Nathan C Sheffield; Michael J Guertin; Chongzhi Zang
Journal:  Bioinformatics       Date:  2018-08-15       Impact factor: 6.937

5.  Analytical Approaches for ATAC-seq Data Analysis.

Authors:  Jason P Smith; Nathan C Sheffield
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6.  Embeddings of genomic region sets capture rich biological associations in lower dimensions.

Authors:  Erfaneh Gharavi; Aaron Gu; Guangtao Zheng; Jason P Smith; Hyun Jae Cho; Aidong Zhang; Donald E Brown; Nathan C Sheffield
Journal:  Bioinformatics       Date:  2021-06-22       Impact factor: 6.931

7.  LOLAweb: a containerized web server for interactive genomic locus overlap enrichment analysis.

Authors:  V P Nagraj; Neal E Magee; Nathan C Sheffield
Journal:  Nucleic Acids Res       Date:  2018-07-02       Impact factor: 16.971

8.  Recommendations for the FAIRification of genomic track metadata.

Authors:  Sveinung Gundersen; Sanjay Boddu; Salvador Capella-Gutierrez; Finn Drabløs; José M Fernández; Radmila Kompova; Kieron Taylor; Dmytro Titov; Daniel Zerbino; Eivind Hovig
Journal:  F1000Res       Date:  2021-04-01

9.  Colocalization analyses of genomic elements: approaches, recommendations and challenges.

Authors:  Chakravarthi Kanduri; Christoph Bock; Sveinung Gundersen; Eivind Hovig; Geir Kjetil Sandve
Journal:  Bioinformatics       Date:  2019-05-01       Impact factor: 6.937

10.  COCOA: coordinate covariation analysis of epigenetic heterogeneity.

Authors:  John T Lawson; Jason P Smith; Stefan Bekiranov; Francine E Garrett-Bakelman; Nathan C Sheffield
Journal:  Genome Biol       Date:  2020-09-07       Impact factor: 17.906

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