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

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.