ChromDragoNN

ChromDragoNN predicts genome-wide chromatin accessibility across diverse cellular contexts by integrating cis-regulatory DNA sequences and context-specific trans-regulator gene expression using multi-modal residual convolutional neural networks.


Key Features:

  • Multi-modal residual neural network architecture: Employs a multi-modal residual convolutional neural network that integrates cis-regulatory DNA sequences and context-specific trans-regulator expression profiles for accessibility prediction.
  • Generalization across cell types: Utilizes the average accessibility of genomic regions across training contexts as an explicit predictor to generalize predictions across diverse cell types.
  • Enhanced prediction strategies: Implements novel model-training strategies to improve genome-wide prediction of both shared and context-specific chromatin accessible sites.
  • Interpretability: Provides interpretability to identify cis- and trans-regulatory elements influencing chromatin accessibility across 123 diverse cellular contexts.

Scientific Applications:

  • Genomics and epigenetics research: Enables genome-wide prediction of chromatin accessibility to support studies in genomics and epigenetics.
  • Transcriptional regulation analysis: Facilitates investigation of transcriptional regulation and the roles of cis- and trans-regulatory elements.
  • Cell-type regulatory inference: Supports analysis of gene expression variability and regulatory mechanisms across different cell types.

Methodology:

Trains multi-modal residual convolutional neural networks on genome-wide chromatin accessibility profiles and gene expression by integrating cis-regulatory DNA sequence inputs and context-specific trans-regulator expression, and incorporates the average accessibility of genomic regions across training contexts as a predictor.

Topics

Details

License:
MIT
Programming Languages:
Python
Added:
11/14/2019
Last Updated:
12/11/2020

Operations

Publications

Nair S, Kim DS, Perricone J, Kundaje A. Integrating regulatory DNA sequence and gene expression to predict genome-wide chromatin accessibility across cellular contexts. Bioinformatics. 2019;35(14):i108-i116. doi:10.1093/bioinformatics/btz352. PMID:31510655. PMCID:PMC6612838.

PMID: 31510655
PMCID: PMC6612838
Funding: - National Institute of Health: 1DP2GM123485, 1R01HG009674, 1U01HG009431