e-TSN
e-TSN maps target-disease associations from biomedical literature and constructs a knowledge graph with bibliometric-based significance and novelty scores to prioritize genes and proteins as therapeutic targets.
Key Features:
- Knowledge Graph Integration: Constructs a knowledge graph integrating heterogeneous biomedical data focused on associations between targets (genes and proteins) and diseases.
- Significance and Novelty Scoring: Computes significance and novelty scores from bibliometric statistics to prioritize candidate disease-related proteins and genes.
- Visualization Capabilities: Produces network visualizations of target-disease relationships and drug-target bioactivity links derived from the knowledge graph.
- Drug-Target Relationship Mapping: Links approved drugs and associated bioactivity data to targets within the knowledge graph.
Scientific Applications:
- Drug Discovery and Development: Prioritizes therapeutic targets by combining knowledge graph associations with bibliometric significance and novelty scores.
- Understanding Disease Mechanisms: Maps interactions between genes/proteins and diseases to support elucidation of disease mechanisms.
- Pandemic Response: Integrates emerging biomedical literature (e.g., COVID-19) to identify potential targets and relevant drug-target links during infectious disease outbreaks.
Methodology:
Applies text mining to extract information from a corpus of biomedical literature, integrates extracted knowledge into a cohesive database/knowledge graph, and derives significance and novelty scores using bibliometric statistics.
Topics
Details
- License:
- Other
- Tool Type:
- web application
- Operating Systems:
- Mac, Linux, Windows
- Programming Languages:
- Python
- Added:
- 1/28/2023
- Last Updated:
- 11/24/2024
Operations
Publications
Feng Z, Shen Z, Li H, Li S. e-TSN: an interactive visual exploration platform for target–disease knowledge mapping from literature. Briefings in Bioinformatics. 2022;23(6). doi:10.1093/bib/bbac465. PMID:36347537. PMCID:PMC9677481.
DOI: 10.1093/bib/bbac465
PMID: 36347537
PMCID: PMC9677481
Funding: - National Natural Science Foundation of China: 81825020, 82150208, 82173690
- Lingang Laboratory: LG-QS-202206-02