iEnhancer-DCSV
iEnhancer-DCSV predicts enhancers and their strength from DNA sequences to support studies of gene regulation.
Key Features:
- Data Encoding: DNA sequences are represented using one-hot encoding and nucleotide chemical property (NCP) features.
- Modified DenseNet: A modified densely connected convolutional network (DenseNet) extracts complex sequence features from the encoded inputs.
- Improved CBAM: An enhanced convolutional block attention module (CBAM) applies channel and spatial attention to prioritize significant features.
- Fully Connected Neural Network: Prioritized features are processed by a fully connected neural network to produce prediction probabilities for enhancer presence and strength.
- Ensemble Learning with Voting: Multiple models are combined via ensemble learning and a voting mechanism to determine final classifications.
Scientific Applications:
- Enhancer identification: Predicts the presence of enhancer regions in genomic sequences.
- Enhancer strength assessment: Predicts relative enhancer strength to inform studies of regulatory element activity.
- Genomic research and large-scale studies: Provides computational predictions of enhancers and their strength to aid investigations of gene regulation and related biological processes.
Methodology:
Sequences are encoded with one-hot and NCP; features are extracted with a modified DenseNet; CBAM performs channel and spatial attention evaluation; a fully connected neural network outputs prediction probabilities for enhancer presence and strength; ensemble learning with a voting mechanism produces final classifications.
Topics
Details
- Cost:
- Free of charge
- Tool Type:
- command-line tool
- Operating Systems:
- Mac, Linux, Windows
- Programming Languages:
- Python
- Added:
- 8/24/2023
- Last Updated:
- 11/24/2024
Operations
Data Inputs & Outputs
Feature extraction
Publications
Jia J, Lei R, Qin L, Wu G, Wei X. iEnhancer-DCSV: Predicting enhancers and their strength based on DenseNet and improved convolutional block attention module. Frontiers in Genetics. 2023;14. doi:10.3389/fgene.2023.1132018. PMID:36936423. PMCID:PMC10014624.