D3GRN
D3GRN infers gene regulatory networks from gene-expression data to elucidate regulatory mechanisms underlying cellular processes and disease by constructing dynamic networks and decomposing regulatory relationships into functional sub-problems.
Key Features:
- Dynamic Network Construction: Models temporal changes and interactions within gene regulatory networks (GRNs) through dynamic network construction.
- Data-Driven Functional Decomposition: Transforms GRN inference into a functional decomposition problem by breaking each target gene's regulatory relationships into sub-problems.
- Algorithm for Revealing Network Interactions (ARNI): Applies ARNI to solve sub-problems and identify candidate interactions from gene-expression data.
- Bootstrapping and Area-Based Scoring: Uses bootstrapping combined with an area-based scoring strategy to refine inferred networks and address limitations of constructing networks solely from unit-level data.
Scientific Applications:
- GRN inference: Inferring gene regulatory networks from gene-expression data to map regulatory relationships among genes.
- Benchmarking and performance evaluation: Validation and comparison on DREAM4 and DREAM5 benchmark datasets with evaluation by Area Under the Precision-Recall Curve (AUPR).
- Systems biology and disease research: Elucidating complex regulatory mechanisms across biological contexts to inform studies of cellular processes and disease mechanisms.
Methodology:
Performs dynamic network construction; decomposes regulatory relationships for each target gene into sub-problems (functional decomposition); applies the Algorithm for Revealing Network Interactions (ARNI) to each sub-problem; and refines inferred networks using bootstrapping and an area-based scoring method.
Topics
Details
- License:
- MIT
- Programming Languages:
- MATLAB
- Added:
- 1/14/2020
- Last Updated:
- 12/17/2020
Operations
Publications
Chen X, Li M, Zheng R, Wu F, Wang J. D3GRN: a data driven dynamic network construction method to infer gene regulatory networks. BMC Genomics. 2019;20(S13). doi:10.1186/s12864-019-6298-5. PMID:31881937. PMCID:PMC6933629.