| Literature DB >> 30878356 |
Michael Ku Yu1, Jianzhu Ma2, Keiichiro Ono2, Fan Zheng2, Samson H Fong3, Aaron Gary2, Jing Chen2, Barry Demchak2, Dexter Pratt2, Trey Ideker4.
Abstract
Systems biology requires not only genome-scale data but also methods to integrate these data into interpretable models. Previously, we developed approaches that organize omics data into a structured hierarchy of cellular components and pathways, called a "data-driven ontology." Such hierarchies recapitulate known cellular subsystems and discover new ones. To broadly facilitate this type of modeling, we report the development of a software library called the Data-Driven Ontology Toolkit (DDOT), consisting of a Python package (https://github.com/idekerlab/ddot) to assemble and analyze ontologies and a web application (http://hiview.ucsd.edu) to visualize them. Using DDOT, we programmatically assemble a compendium of ontologies for 652 diseases by integrating gene-disease mappings with a gene similarity network derived from omics data. For example, the ontology for Fanconi anemia describes known and novel disease mechanisms in its hierarchy of 194 genes and 74 subsystems. DDOT provides an easy interface to share ontologies online at the Network Data Exchange.Entities:
Keywords: disease network; fanconi anemia; gene ontology; hierarchical; interaction network; multi-scale
Year: 2019 PMID: 30878356 DOI: 10.1016/j.cels.2019.02.003
Source DB: PubMed Journal: Cell Syst ISSN: 2405-4712 Impact factor: 10.304