DeeReCT-TSS

DeeReCT-TSS identifies transcription start sites (TSSs) genome-wide by integrating DNA sequences and RNA-seq data with deep learning to provide precise TSS annotation for studies of gene regulation.


Key Features:

  • Deep learning approach: Employs a deep learning framework that integrates sequence and expression features to predict TSSs genome-wide.
  • Integration of multi-source data: Combines genomic DNA sequences and conventional RNA-seq data to improve TSS detection and reflect transcriptional activity across cell types.
  • Meta-learning-based extension: Implements a meta-learning extension to enable simultaneous annotation across multiple cell types and to identify cell-type-specific TSSs.
  • Validation and precision: Validated against independent ENCODE datasets by correlating predicted TSSs with experimentally defined TSS chromatin states, demonstrating high precision.

Scientific Applications:

  • Genome-wide TSS annotation: Generates precise annotations of TSSs across the genome to support studies of promoter architecture and transcriptional regulation.
  • Cell-type-specific TSS discovery: Identifies cell-type-specific TSSs to investigate differential promoter usage during cellular differentiation and disease.
  • Integration with RNA-seq analyses: Links sequence-based TSS predictions with RNA-seq evidence to study transcription initiation and expression dynamics.

Methodology:

A deep learning model trained on DNA sequences and RNA-seq data, a meta-learning-based extension for multi-cell-type annotation, and validation by comparison to ENCODE-defined TSS chromatin states.

Topics

Details

Tool Type:
command-line tool
Operating Systems:
Mac, Linux, Windows
Programming Languages:
Python, Shell
Added:
11/3/2021
Last Updated:
11/3/2021

Operations

Publications

Zhou J, zhang b, Li H, Zhou L, Li Z, Long Y, Han W, Wang M, Cui H, Chen W, Gao X. DeeReCT-TSS: A novel meta-learning-based method annotates TSS in multiple cell types based on DNA sequences and RNA-seq data. Unknown Journal. 2021. doi:10.21203/rs.3.rs-640669/v1.