Abstract
Functional explication of genes is of great scientific value. However, conventional methods have challenges for those genes thatmay affect biological processes but are not annotated in public databases. Here, we developed a novel explainable gene ontology fingerprint (XGOF) method to automatically produce knowledge networks on biomedical literature in a given field which quantitatively characterizes
the association between genes and ontologies. XGOF provides systematic knowledge for the potential function of genes and ontologically compares similarities and discrepancies in different disease-XGOFs integrating omics data. More importantly, XGOF can not only help to infer major cellular components
in a disease microenvironment but also reveal novel gene panels or functions for in-depth experimental research where few explicit connections to diseases have previously been described in the literature. The reliability of XGOF is validated in four application scenarios, indicating a unique perspective of integrating
text and data mining, with the potential to accelerate scientific discovery.
| Original language | English |
|---|---|
| Article number | 106356 |
| Journal | iScience |
| Volume | 26 |
| Issue number | 4 |
| DOIs | |
| Publication status | Published - 7 Mar 2023 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Cancer
- bioinformatics
- cancer
- Data processing in systems biology
- Biological sciences tools
ASJC Scopus subject areas
- Multidisciplinary
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