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Bringing radiomics into a multi-omics framework for a comprehensive genotype–phenotype characterization of oncological diseases

Genomic and radiomic data integration, namely radiogenomics, can provide meaningful knowledge in cancer diagnosis, prognosis and treatment. Despite several data structures based on multi-layer architecture proposed to combine multi-omic biological information, none of these has been designed and ass...

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Autores principales: Zanfardino, Mario, Franzese, Monica, Pane, Katia, Cavaliere, Carlo, Monti, Serena, Esposito, Giuseppina, Salvatore, Marco, Aiello, Marco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6778975/
https://www.ncbi.nlm.nih.gov/pubmed/31590671
http://dx.doi.org/10.1186/s12967-019-2073-2
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author Zanfardino, Mario
Franzese, Monica
Pane, Katia
Cavaliere, Carlo
Monti, Serena
Esposito, Giuseppina
Salvatore, Marco
Aiello, Marco
author_facet Zanfardino, Mario
Franzese, Monica
Pane, Katia
Cavaliere, Carlo
Monti, Serena
Esposito, Giuseppina
Salvatore, Marco
Aiello, Marco
author_sort Zanfardino, Mario
collection PubMed
description Genomic and radiomic data integration, namely radiogenomics, can provide meaningful knowledge in cancer diagnosis, prognosis and treatment. Despite several data structures based on multi-layer architecture proposed to combine multi-omic biological information, none of these has been designed and assessed to include radiomic data as well. To meet this need, we propose to use the MultiAssayExperiment (MAE), an R package that provides data structures and methods for manipulating and integrating multi-assay experiments, as a suitable tool to manage radiogenomic experiment data. To this aim, we first examine the role of radiogenomics in cancer phenotype definition, then the current state of radiogenomics data integration in public repository and, finally, challenges and limitations of including radiomics in MAE, designing an extended framework and showing its application on a case study from the TCGA-TCIA archives. Radiomic and genomic data from 91 patients have been successfully integrated in a single MAE object, demonstrating the suitability of the MAE data structure as container of radiogenomic data.
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spelling pubmed-67789752019-10-11 Bringing radiomics into a multi-omics framework for a comprehensive genotype–phenotype characterization of oncological diseases Zanfardino, Mario Franzese, Monica Pane, Katia Cavaliere, Carlo Monti, Serena Esposito, Giuseppina Salvatore, Marco Aiello, Marco J Transl Med Review Genomic and radiomic data integration, namely radiogenomics, can provide meaningful knowledge in cancer diagnosis, prognosis and treatment. Despite several data structures based on multi-layer architecture proposed to combine multi-omic biological information, none of these has been designed and assessed to include radiomic data as well. To meet this need, we propose to use the MultiAssayExperiment (MAE), an R package that provides data structures and methods for manipulating and integrating multi-assay experiments, as a suitable tool to manage radiogenomic experiment data. To this aim, we first examine the role of radiogenomics in cancer phenotype definition, then the current state of radiogenomics data integration in public repository and, finally, challenges and limitations of including radiomics in MAE, designing an extended framework and showing its application on a case study from the TCGA-TCIA archives. Radiomic and genomic data from 91 patients have been successfully integrated in a single MAE object, demonstrating the suitability of the MAE data structure as container of radiogenomic data. BioMed Central 2019-10-07 /pmc/articles/PMC6778975/ /pubmed/31590671 http://dx.doi.org/10.1186/s12967-019-2073-2 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Zanfardino, Mario
Franzese, Monica
Pane, Katia
Cavaliere, Carlo
Monti, Serena
Esposito, Giuseppina
Salvatore, Marco
Aiello, Marco
Bringing radiomics into a multi-omics framework for a comprehensive genotype–phenotype characterization of oncological diseases
title Bringing radiomics into a multi-omics framework for a comprehensive genotype–phenotype characterization of oncological diseases
title_full Bringing radiomics into a multi-omics framework for a comprehensive genotype–phenotype characterization of oncological diseases
title_fullStr Bringing radiomics into a multi-omics framework for a comprehensive genotype–phenotype characterization of oncological diseases
title_full_unstemmed Bringing radiomics into a multi-omics framework for a comprehensive genotype–phenotype characterization of oncological diseases
title_short Bringing radiomics into a multi-omics framework for a comprehensive genotype–phenotype characterization of oncological diseases
title_sort bringing radiomics into a multi-omics framework for a comprehensive genotype–phenotype characterization of oncological diseases
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6778975/
https://www.ncbi.nlm.nih.gov/pubmed/31590671
http://dx.doi.org/10.1186/s12967-019-2073-2
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