代谢组学
计算机科学
工作台
背景(考古学)
数据科学
数据集成
数据挖掘
数据共享
原始数据
聚类分析
Python(编程语言)
计算生物学
系统生物学
生物学数据
重新使用
基因组学
注释
仿形(计算机编程)
数据整理
元数据
生物信息学
资源(消歧)
作者
Cecilia Wieder,Eloisa Rocha Liedl,Thomas Payne,Ozgur Yurekten,Callum Martin,Felix Xavier Amaladoss,Noemi Tejera,Wanchang Lin,Yasin El Abiead,Pieter Dorrestein,Claire O’Donovan,Juan Antonio Vizcaíno,Warwick Dunn,Timothy Ebbels
出处
期刊:Metabolomics
[Springer Science+Business Media]
日期:2026-07-15
卷期号:22 (4)
标识
DOI:10.1007/s11306-026-02507-4
摘要
INTRODUCTION: Public metabolomics data repositories such as MetaboLights and Metabolomics Workbench host rapidly growing volumes of raw data, processed results, and metadata. As data deposition becomes a prerequisite for funding and publication, there is an increasing need for tools that enable integration and joint reanalysis of datasets across studies to maximise reuse and reproducibility. OBJECTIVES: This study aims to enable large-scale integrative meta-analysis of public metabolomics data, exploiting harmonised metabolite annotations to identify robust multi-study metabolite and pathway signatures and to provide global visual overviews of repository content. METHODS: We developed a network-based integration framework operating at both the study (dataset) level and the metabolite or pathway level. Metabolite-level meta-networks integrate studies with shared biological context using co-occurrences of differential metabolites represented as bipartite graphs. Study-level networks compare observed metabolites for overall repository exploration. Networks can be explored interactively using a dedicated Python Dash app available at https://github.com/EloisaRL/Metabolomic-data-analysis-app/tree/main . RESULTS: As an example, the approach was applied to six COVID-19 plasma datasets from MetaboLights generated using LC-MS and NMR. Ten metabolites were identified as differential in at least three studies, including consistently up-regulated pyroglutamic acid, in agreement with the literature. Pathway-level networks provided an overview of shared biological processes across studies. A global network of 1,181 studies in Metabolomics Workbench demonstrated clustering by assay coverage and associated metadata, as expected. CONCLUSION: Network-based integration of harmonised metabolomics data enables robust cross-study analyses and highlights the critical importance of standardised annotation pipelines. Such approaches enhance the reuse, reproducibility, and impact of public metabolomics datasets, accelerating biological discovery.
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