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