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How to interpret and integrate multi-omics data at systems level
Current parallel sequencing technologies generate biological sequence data explosively and enable omics studies that analyze collective biological features. The more omics data that is accumulated, the more they show the regulatory complexity of biological phenotypes. This high order regulatory comp...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7048189/ https://www.ncbi.nlm.nih.gov/pubmed/32158610 http://dx.doi.org/10.1080/19768354.2020.1721321 |
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author | Jung, Gun Tae Kim, Kwang-Pyo Kim, Kwoneel |
author_facet | Jung, Gun Tae Kim, Kwang-Pyo Kim, Kwoneel |
author_sort | Jung, Gun Tae |
collection | PubMed |
description | Current parallel sequencing technologies generate biological sequence data explosively and enable omics studies that analyze collective biological features. The more omics data that is accumulated, the more they show the regulatory complexity of biological phenotypes. This high order regulatory complexity needs systems-level approaches, including network analysis, to understand it. There are a series of layers in the omics field that are closely connected to each other as described in ‘central dogma.’ We, therefore, have to not only interpret each single omics layer but also to integrate multi-omics layers systematically to get a full picture of the regulatory landscape of the biological phenotype. Especially, individual omics data has their own adequate biological network to apply systematic analysis appropriately. A full regulatory landscape can only be obtained when multi-omics data are incorporated within adequate networks. In this review, we discuss how to interpret and integrate multi-omics data systematically using recent studies. We also propose an analysis framework for systematic multi-omics interpretation by centering on the transcriptional core regulator, which can be incorporated in all omics networks. |
format | Online Article Text |
id | pubmed-7048189 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-70481892020-03-10 How to interpret and integrate multi-omics data at systems level Jung, Gun Tae Kim, Kwang-Pyo Kim, Kwoneel Anim Cells Syst (Seoul) Genes & Genomics Current parallel sequencing technologies generate biological sequence data explosively and enable omics studies that analyze collective biological features. The more omics data that is accumulated, the more they show the regulatory complexity of biological phenotypes. This high order regulatory complexity needs systems-level approaches, including network analysis, to understand it. There are a series of layers in the omics field that are closely connected to each other as described in ‘central dogma.’ We, therefore, have to not only interpret each single omics layer but also to integrate multi-omics layers systematically to get a full picture of the regulatory landscape of the biological phenotype. Especially, individual omics data has their own adequate biological network to apply systematic analysis appropriately. A full regulatory landscape can only be obtained when multi-omics data are incorporated within adequate networks. In this review, we discuss how to interpret and integrate multi-omics data systematically using recent studies. We also propose an analysis framework for systematic multi-omics interpretation by centering on the transcriptional core regulator, which can be incorporated in all omics networks. Taylor & Francis 2020-01-30 /pmc/articles/PMC7048189/ /pubmed/32158610 http://dx.doi.org/10.1080/19768354.2020.1721321 Text en © 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Genes & Genomics Jung, Gun Tae Kim, Kwang-Pyo Kim, Kwoneel How to interpret and integrate multi-omics data at systems level |
title | How to interpret and integrate multi-omics data at systems level |
title_full | How to interpret and integrate multi-omics data at systems level |
title_fullStr | How to interpret and integrate multi-omics data at systems level |
title_full_unstemmed | How to interpret and integrate multi-omics data at systems level |
title_short | How to interpret and integrate multi-omics data at systems level |
title_sort | how to interpret and integrate multi-omics data at systems level |
topic | Genes & Genomics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7048189/ https://www.ncbi.nlm.nih.gov/pubmed/32158610 http://dx.doi.org/10.1080/19768354.2020.1721321 |
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