DeepGenGrep

DeepGenGrep identifies genomic signals and regions (GSRs) from DNA sequences using a hybrid deep learning architecture to improve annotation of gene structure, regulation, and function.


Key Features:

  • Hybrid Neural Network Architecture: Combines a three-layer convolutional neural network (CNN) and a two-layer long short-term memory (LSTM) network to capture local patterns and sequential dependencies and learn feature representations from DNA sequences.
  • Multi-GSR Prediction: Systematically identifies multiple genomic signals and regions, including polyadenylation signals, translation initiation sites, and splice sites.
  • Cross-Species Benchmarking: Evaluated on Homo sapiens, Mus musculus, Bos taurus, and Drosophila melanogaster and demonstrated superior performance compared to several state-of-the-art approaches.
  • High-Throughput Analysis: Facilitates high-throughput, cost-effective prediction and annotation of eukaryotic genomes.

Scientific Applications:

  • Gene Regulation and Functional Genomics: Prediction of GSRs to inform studies of gene structure, transcriptional and post-transcriptional regulation.
  • Genome Annotation: Annotation of polyadenylation signals, translation initiation sites, and splice sites in eukaryotic genomes including human, mouse, cattle, and Drosophila.
  • Comparative Genomics and Method Benchmarking: Cross-species analyses to compare genomic signals and to benchmark prediction performance against existing methods.

Methodology:

DeepGenGrep employs a hybrid deep learning framework combining a three-layer CNN and a two-layer LSTM to capture spatial and temporal patterns in genomic sequences for GSR prediction.

Topics

Details

License:
Other
Cost:
Free of charge
Tool Type:
command-line tool, web application
Operating Systems:
Mac, Linux, Windows
Programming Languages:
Python
Added:
10/4/2022
Last Updated:
11/24/2024

Operations

Publications

Liu Q, Fang H, Wang X, Wang M, Li S, Coin LJM, Li F, Song J. DeepGenGrep: a general deep learning-based predictor for multiple genomic signals and regions. Bioinformatics. 2022;38(17):4053-4061. doi:10.1093/bioinformatics/btac454. PMID:35799358.

PMID: 35799358
Funding: - National Natural Science Foundation of China: 61972322

Links