Return
OptimDase: An Algorithm for Predicting DNA Binding Sites with Combined Feature Encoding
DOI:10.1007/s12539-025-00704-8.png)
Abstract
En 中文
Identifying DNA binding sites remains a critical task in bioinformatics, with applications ranging from gene regulation studies to drug design. Although progress has been made in computational techniques, we still face challenges such as data complexity and prediction accuracy. In this paper, we introduce OptimDase, a new algorithm. It integrates feature encoding with optimum decision-making frameworks to improve DNA binding site prediction. OptimDase integrates multi-scale scanning and feature selection strategies, making it highly effective for both classification and regression tasks. Our experiments demonstrate that OptimDase achieves superior performance with an accuracy of 0.8943 in classification tasks and an RMSE of 0.0054 in regression tasks, outperforming existing algorithms in key evaluation metrics. These results highlight OptimDase’s portability and robustness, making it an effective solution for identifying DNA binding sites and advancing the applications of drug design.
Keywords:
DNA binding site
Machine learning
optimum decision-making
Site-specific recombination
combined feature encoding
Journal
I
IF:
3.9
Papers:
962
Citations:
1.5K
Organization
Cited Papers
Selective deployment of transcription factor paralogs with submaximal strength facilitates gene regulation in the immune system
NATURE IMMUNOLOGY
IF27.6
Proteins Recognizing DNA: Structural Uniqueness and Versatility of DNA-Binding Domains in Stem Cell Transcription Factors
Genes
IF0
Five-Vertebrate ChIP-seq Reveals the Evolutionary Dynamics of Transcription Factor Binding
Science
IF0

