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Identification of functional gene modules by integrating multi-omics data and known molecular interactions
Multi-omics data integration has emerged as a promising approach to identify patient subgroups. However, in terms of grouping genes (or gene products) into co-expression modules, data integration methods suffer from two main drawbacks. First, most existing methods only consider genes or samples meas...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9902936/ https://www.ncbi.nlm.nih.gov/pubmed/36760999 http://dx.doi.org/10.3389/fgene.2023.1082032 |
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author | Chen, Xiaoqing Han, Mingfei Li, Yingxing Li, Xiao Zhang, Jiaqi Zhu, Yunping |
author_facet | Chen, Xiaoqing Han, Mingfei Li, Yingxing Li, Xiao Zhang, Jiaqi Zhu, Yunping |
author_sort | Chen, Xiaoqing |
collection | PubMed |
description | Multi-omics data integration has emerged as a promising approach to identify patient subgroups. However, in terms of grouping genes (or gene products) into co-expression modules, data integration methods suffer from two main drawbacks. First, most existing methods only consider genes or samples measured in all different datasets. Second, known molecular interactions (e.g., transcriptional regulatory interactions, protein–protein interactions and biological pathways) cannot be utilized to assist in module detection. Herein, we present a novel data integration framework, Correlation-based Local Approximation of Membership (CLAM), which provides two methodological innovations to address these limitations: 1) constructing a trans-omics neighborhood matrix by integrating multi-omics datasets and known molecular interactions, and 2) using a local approximation procedure to define gene modules from the matrix. Applying Correlation-based Local Approximation of Membership to human colorectal cancer (CRC) and mouse B-cell differentiation multi-omics data obtained from The Cancer Genome Atlas (TCGA), Clinical Proteomics Tumor Analysis Consortium (CPTAC), Gene Expression Omnibus (GEO) and ProteomeXchange database, we demonstrated its superior ability to recover biologically relevant modules and gene ontology (GO) terms. Further investigation of the colorectal cancer modules revealed numerous transcription factors and KEGG pathways that played crucial roles in colorectal cancer progression. Module-based survival analysis constructed four survival-related networks in which pairwise gene correlations were significantly correlated with colorectal cancer patient survival. Overall, the series of evaluations demonstrated the great potential of Correlation-based Local Approximation of Membership for identifying modular biomarkers for complex diseases. We implemented Correlation-based Local Approximation of Membership as a user-friendly application available at https://github.com/free1234hm/CLAM. |
format | Online Article Text |
id | pubmed-9902936 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-99029362023-02-08 Identification of functional gene modules by integrating multi-omics data and known molecular interactions Chen, Xiaoqing Han, Mingfei Li, Yingxing Li, Xiao Zhang, Jiaqi Zhu, Yunping Front Genet Genetics Multi-omics data integration has emerged as a promising approach to identify patient subgroups. However, in terms of grouping genes (or gene products) into co-expression modules, data integration methods suffer from two main drawbacks. First, most existing methods only consider genes or samples measured in all different datasets. Second, known molecular interactions (e.g., transcriptional regulatory interactions, protein–protein interactions and biological pathways) cannot be utilized to assist in module detection. Herein, we present a novel data integration framework, Correlation-based Local Approximation of Membership (CLAM), which provides two methodological innovations to address these limitations: 1) constructing a trans-omics neighborhood matrix by integrating multi-omics datasets and known molecular interactions, and 2) using a local approximation procedure to define gene modules from the matrix. Applying Correlation-based Local Approximation of Membership to human colorectal cancer (CRC) and mouse B-cell differentiation multi-omics data obtained from The Cancer Genome Atlas (TCGA), Clinical Proteomics Tumor Analysis Consortium (CPTAC), Gene Expression Omnibus (GEO) and ProteomeXchange database, we demonstrated its superior ability to recover biologically relevant modules and gene ontology (GO) terms. Further investigation of the colorectal cancer modules revealed numerous transcription factors and KEGG pathways that played crucial roles in colorectal cancer progression. Module-based survival analysis constructed four survival-related networks in which pairwise gene correlations were significantly correlated with colorectal cancer patient survival. Overall, the series of evaluations demonstrated the great potential of Correlation-based Local Approximation of Membership for identifying modular biomarkers for complex diseases. We implemented Correlation-based Local Approximation of Membership as a user-friendly application available at https://github.com/free1234hm/CLAM. Frontiers Media S.A. 2023-01-24 /pmc/articles/PMC9902936/ /pubmed/36760999 http://dx.doi.org/10.3389/fgene.2023.1082032 Text en Copyright © 2023 Chen, Han, Li, Li, Zhang and Zhu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Genetics Chen, Xiaoqing Han, Mingfei Li, Yingxing Li, Xiao Zhang, Jiaqi Zhu, Yunping Identification of functional gene modules by integrating multi-omics data and known molecular interactions |
title | Identification of functional gene modules by integrating multi-omics data and known molecular interactions |
title_full | Identification of functional gene modules by integrating multi-omics data and known molecular interactions |
title_fullStr | Identification of functional gene modules by integrating multi-omics data and known molecular interactions |
title_full_unstemmed | Identification of functional gene modules by integrating multi-omics data and known molecular interactions |
title_short | Identification of functional gene modules by integrating multi-omics data and known molecular interactions |
title_sort | identification of functional gene modules by integrating multi-omics data and known molecular interactions |
topic | Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9902936/ https://www.ncbi.nlm.nih.gov/pubmed/36760999 http://dx.doi.org/10.3389/fgene.2023.1082032 |
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