Deep4mC
Deep4mC predicts DNA N4-methylcytosine (4mC) sites in genomic sequences to support investigation of epigenetic regulation across multiple species.
Key Features:
- Deep learning-based prediction: Leverages convolutional neural networks (CNNs) to predict 4mC sites from sequence-derived features.
- Representative feature set: Incorporates four representative features that were systematically evaluated for predictive capacity across six species.
- Feature optimization and reinforcement learning: Employs feature selection strategies and reinforcement learning techniques to enhance model performance.
- Benchmark validation and performance metrics: Validated on a representative benchmark dataset achieving average area under curve (AUC) values greater than 0.9 across tested species, with AUC improvements of 10.14% to 46.21% over previous tools.
- Bootstrapping for small sample sizes: Extends the deep learning framework using a bootstrapping method to improve robustness for species with limited data.
Scientific Applications:
- Epigenetic research: Enables identification of putative 4mC sites to study epigenetic regulation of processes such as DNA replication, cell cycle regulation, and gene expression.
- Comparative genomics: Facilitates cross-species identification of potential 4mC modifications for comparative genomic analyses across the six evaluated species.
- Biomarker discovery: Supports discovery of candidate 4mC sites that may serve as biomarkers in disease research and diagnostics due to high predictive accuracy.
Methodology:
Convolutional neural networks trained on four representative features with feature selection and reinforcement learning, evaluated on a benchmark dataset using AUC metrics, and supplemented by bootstrapping for small-sample species.
Topics
Details
- Tool Type:
- web application
- Added:
- 1/18/2021
- Last Updated:
- 11/24/2024
Operations
Publications
Xu H, Jia P, Zhao Z. Deep4mC: systematic assessment and computational prediction for DNA N4-methylcytosine sites by deep learning. Briefings in Bioinformatics. 2020;22(3). doi:10.1093/bib/bbaa099. PMID:32578842. PMCID:PMC8138820.
DOI: 10.1093/bib/bbaa099
PMID: 32578842
PMCID: PMC8138820
Funding: - Cancer Genomics Core funded by the Cancer Prevention and Research Institute of Texas: CPRIT RP170668, RP180734
- National Institutes of Health: R01LM012806