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From ‘Omics to Multi-omics Technologies: the Discovery of Novel Causal Mediators

PURPOSE OF REVIEW: ‘Omics studies provide a comprehensive characterisation of a biological entity, such as the genome, epigenome, transcriptome, proteome, metabolome, or microbiome. This review covers the unique properties of these types of ‘omics and their roles as causal mediators in cardiovascula...

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Autores principales: Mohammadi-Shemirani, Pedrum, Sood, Tushar, Paré, Guillaume
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9807989/
https://www.ncbi.nlm.nih.gov/pubmed/36595202
http://dx.doi.org/10.1007/s11883-022-01078-8
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author Mohammadi-Shemirani, Pedrum
Sood, Tushar
Paré, Guillaume
author_facet Mohammadi-Shemirani, Pedrum
Sood, Tushar
Paré, Guillaume
author_sort Mohammadi-Shemirani, Pedrum
collection PubMed
description PURPOSE OF REVIEW: ‘Omics studies provide a comprehensive characterisation of a biological entity, such as the genome, epigenome, transcriptome, proteome, metabolome, or microbiome. This review covers the unique properties of these types of ‘omics and their roles as causal mediators in cardiovascular disease. Moreover, applications and challenges of integrating multiple types of ‘omics data to increase predictive power, improve causal inference, and elucidate biological mechanisms are discussed. RECENT FINDINGS: Multi-omics approaches are growing in adoption as they provide orthogonal evidence and overcome the limitations of individual types of ‘omics data. Studies with multiple types of ‘omics data have improved the diagnosis and prediction of disease states and afforded a deeper understanding of underlying pathophysiological mechanisms, beyond any single type of ‘omics data. For instance, disease-associated loci in the genome can be supplemented with other ‘omics to prioritise causal genes and understand the function of non-coding variants. Alternatively, techniques, such as Mendelian randomisation, can leverage genetics to provide evidence supporting a causal role for disease-associated molecules, and elucidate their role in disease pathogenesis. SUMMARY: As technologies improve, costs for ‘omics studies will continue to fall and datasets will become increasingly accessible to researchers. The intrinsically unbiased nature of ‘omics data is well-suited to exploratory analyses that discover causal mediators of disease, and multi-omics is an emerging discipline that leverages the strengths of each type of ‘omics data to provide insights greater than the sum of its parts.
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spelling pubmed-98079892023-01-04 From ‘Omics to Multi-omics Technologies: the Discovery of Novel Causal Mediators Mohammadi-Shemirani, Pedrum Sood, Tushar Paré, Guillaume Curr Atheroscler Rep Article PURPOSE OF REVIEW: ‘Omics studies provide a comprehensive characterisation of a biological entity, such as the genome, epigenome, transcriptome, proteome, metabolome, or microbiome. This review covers the unique properties of these types of ‘omics and their roles as causal mediators in cardiovascular disease. Moreover, applications and challenges of integrating multiple types of ‘omics data to increase predictive power, improve causal inference, and elucidate biological mechanisms are discussed. RECENT FINDINGS: Multi-omics approaches are growing in adoption as they provide orthogonal evidence and overcome the limitations of individual types of ‘omics data. Studies with multiple types of ‘omics data have improved the diagnosis and prediction of disease states and afforded a deeper understanding of underlying pathophysiological mechanisms, beyond any single type of ‘omics data. For instance, disease-associated loci in the genome can be supplemented with other ‘omics to prioritise causal genes and understand the function of non-coding variants. Alternatively, techniques, such as Mendelian randomisation, can leverage genetics to provide evidence supporting a causal role for disease-associated molecules, and elucidate their role in disease pathogenesis. SUMMARY: As technologies improve, costs for ‘omics studies will continue to fall and datasets will become increasingly accessible to researchers. The intrinsically unbiased nature of ‘omics data is well-suited to exploratory analyses that discover causal mediators of disease, and multi-omics is an emerging discipline that leverages the strengths of each type of ‘omics data to provide insights greater than the sum of its parts. Springer US 2023-01-03 2023 /pmc/articles/PMC9807989/ /pubmed/36595202 http://dx.doi.org/10.1007/s11883-022-01078-8 Text en © The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2022, Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Article
Mohammadi-Shemirani, Pedrum
Sood, Tushar
Paré, Guillaume
From ‘Omics to Multi-omics Technologies: the Discovery of Novel Causal Mediators
title From ‘Omics to Multi-omics Technologies: the Discovery of Novel Causal Mediators
title_full From ‘Omics to Multi-omics Technologies: the Discovery of Novel Causal Mediators
title_fullStr From ‘Omics to Multi-omics Technologies: the Discovery of Novel Causal Mediators
title_full_unstemmed From ‘Omics to Multi-omics Technologies: the Discovery of Novel Causal Mediators
title_short From ‘Omics to Multi-omics Technologies: the Discovery of Novel Causal Mediators
title_sort from ‘omics to multi-omics technologies: the discovery of novel causal mediators
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9807989/
https://www.ncbi.nlm.nih.gov/pubmed/36595202
http://dx.doi.org/10.1007/s11883-022-01078-8
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