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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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 |
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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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1724656393139519488 |