deepC
deepC predicts Hi-C chromatin interactions from megabase-scale DNA sequences to model three-dimensional genome folding and to assess effects of genetic variation on chromatin architecture.
Key Features:
- Hi-C interaction prediction: Predicts Hi-C chromatin interactions from megabase-scale DNA sequences.
- Transfer-learning-based deep learning: Implements a transfer-learning-based deep neural network framework to learn sequence determinants of genome folding.
- Domain boundary identification: Identifies domain boundaries at high resolution from sequence-based predictions.
- Variant impact prediction: Predicts the impact of large-scale structural variations and single base-pair changes on three-dimensional genome architecture.
- Noncoding variation interpretation: Interprets noncoding genetic variation in the context of three-dimensional genome organization.
Scientific Applications:
- Noncoding genetic variation analysis: Assess functional consequences of noncoding genetic variation using predicted three-dimensional genome structure.
- Structural genomics: Study effects of structural variants on chromatin folding and domain boundaries.
- Gene regulation research: Investigate mechanisms of gene regulation driven by three-dimensional genome organization.
- Genetic variation studies: Analyze how single base-pair changes and larger variants influence chromosomal organization and regulatory architecture.
Methodology:
Uses a transfer-learning-based deep neural network trained on megabase-scale DNA sequences to predict Hi-C chromatin interactions and domain boundaries and to evaluate effects of structural variations and single base-pair changes.
Topics
Details
- License:
- GPL-3.0
- Tool Type:
- command-line tool
- Added:
- 1/18/2021
- Last Updated:
- 11/24/2024
Operations
Publications
Schwessinger R, Gosden M, Downes D, Brown RC, Oudelaar AM, Telenius J, Teh YW, Lunter G, Hughes JR. DeepC: predicting 3D genome folding using megabase-scale transfer learning. Nature Methods. 2020;17(11):1118-1124. doi:10.1038/s41592-020-0960-3. PMID:33046896. PMCID:PMC7610627.
PMID: 33046896
PMCID: PMC7610627
Funding: - RCUK | Medical Research Council: MC_UU_00016/14
- Wellcome Trust: 105605/Z/14/Z, 203728/Z/16/Z