MOTA: Network-Based Multi-Omic Data Integration for Biomarker Discovery

The recent advancement of omic technologies provides researchers with the possibility to search for disease-associated biomarkers at the system level. The integrative analysis of data from a large number of molecules involved at various layers of the biological system offers a great opportunity to r...

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Main Authors: Ziling Fan, Yuan Zhou, Habtom W. Ressom
Format: Article
Language:English
Published: MDPI AG 2020-04-01
Series:Metabolites
Subjects:
Online Access:https://www.mdpi.com/2218-1989/10/4/144
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spelling doaj-24c8a12f12c441459b8a0e579b79168c2020-11-25T03:10:55ZengMDPI AGMetabolites2218-19892020-04-011014414410.3390/metabo10040144MOTA: Network-Based Multi-Omic Data Integration for Biomarker DiscoveryZiling Fan0Yuan Zhou1Habtom W. Ressom2Department of Biochemistry and Molecular and Cellular Biology, Georgetown University Medical Center, Washington, DC 20057, USADepartment of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, DC 20057, USADepartment of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, DC 20057, USAThe recent advancement of omic technologies provides researchers with the possibility to search for disease-associated biomarkers at the system level. The integrative analysis of data from a large number of molecules involved at various layers of the biological system offers a great opportunity to rank disease biomarker candidates. In this paper, we propose MOTA, a network-based method that uses data acquired at multiple layers to rank candidate disease biomarkers. The networks constructed by MOTA allow users to investigate the biological significance of the top-ranked biomarker candidates. We evaluated the performance of MOTA in ranking disease-associated molecules from three sets of multi-omic data representing three cohorts of hepatocellular carcinoma (HCC) cases and controls with liver cirrhosis. The results demonstrate that MOTA allows the identification of more top-ranked metabolite biomarker candidates that are shared by two different cohorts compared to traditional statistical methods. Moreover, the mRNA candidates top-ranked by MOTA comprise more cancer driver genes compared to those ranked by traditional differential expression methods.https://www.mdpi.com/2218-1989/10/4/144multi-omic integrationdifferential networkmetabolomicstranscriptomics
collection DOAJ
language English
format Article
sources DOAJ
author Ziling Fan
Yuan Zhou
Habtom W. Ressom
spellingShingle Ziling Fan
Yuan Zhou
Habtom W. Ressom
MOTA: Network-Based Multi-Omic Data Integration for Biomarker Discovery
Metabolites
multi-omic integration
differential network
metabolomics
transcriptomics
author_facet Ziling Fan
Yuan Zhou
Habtom W. Ressom
author_sort Ziling Fan
title MOTA: Network-Based Multi-Omic Data Integration for Biomarker Discovery
title_short MOTA: Network-Based Multi-Omic Data Integration for Biomarker Discovery
title_full MOTA: Network-Based Multi-Omic Data Integration for Biomarker Discovery
title_fullStr MOTA: Network-Based Multi-Omic Data Integration for Biomarker Discovery
title_full_unstemmed MOTA: Network-Based Multi-Omic Data Integration for Biomarker Discovery
title_sort mota: network-based multi-omic data integration for biomarker discovery
publisher MDPI AG
series Metabolites
issn 2218-1989
publishDate 2020-04-01
description The recent advancement of omic technologies provides researchers with the possibility to search for disease-associated biomarkers at the system level. The integrative analysis of data from a large number of molecules involved at various layers of the biological system offers a great opportunity to rank disease biomarker candidates. In this paper, we propose MOTA, a network-based method that uses data acquired at multiple layers to rank candidate disease biomarkers. The networks constructed by MOTA allow users to investigate the biological significance of the top-ranked biomarker candidates. We evaluated the performance of MOTA in ranking disease-associated molecules from three sets of multi-omic data representing three cohorts of hepatocellular carcinoma (HCC) cases and controls with liver cirrhosis. The results demonstrate that MOTA allows the identification of more top-ranked metabolite biomarker candidates that are shared by two different cohorts compared to traditional statistical methods. Moreover, the mRNA candidates top-ranked by MOTA comprise more cancer driver genes compared to those ranked by traditional differential expression methods.
topic multi-omic integration
differential network
metabolomics
transcriptomics
url https://www.mdpi.com/2218-1989/10/4/144
work_keys_str_mv AT zilingfan motanetworkbasedmultiomicdataintegrationforbiomarkerdiscovery
AT yuanzhou motanetworkbasedmultiomicdataintegrationforbiomarkerdiscovery
AT habtomwressom motanetworkbasedmultiomicdataintegrationforbiomarkerdiscovery
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