AUCpreD
AUCpreD predicts intrinsically disordered regions (IDRs) in protein sequences using a Deep Convolutional Neural Fields (DeepCNF) machine learning framework without requiring sequence profiles.
Key Features:
- Sequence-Based IDR Prediction: Predicts intrinsically disordered regions directly from protein sequences without requiring sequence profile generation.
- DeepCNF Architecture: Implements Deep Convolutional Neural Fields that integrate deep convolutional neural networks (DCNN) with conditional random fields (CRF) to model sequence–structure relationships and residue dependencies.
- AUC-Maximization Training Strategy: Optimizes model training by maximizing the area under the ROC curve (AUC) to address class imbalance between ordered and disordered residues.
- Proteome-Scale Analysis: Enables large-scale prediction of intrinsically disordered regions across entire proteomes.
Scientific Applications:
- Protein Disorder Annotation: Identifies intrinsically disordered regions within protein sequences for functional and structural analysis.
- Proteome-Wide Structural Analysis: Supports large-scale identification of disordered regions across complete proteomes.
- Protein Structure–Function Studies: Assists investigations of biological processes involving intrinsically disordered protein regions.
Methodology:
AUCpreD formulates intrinsically disordered region prediction as a sequence labeling problem and applies Deep Convolutional Neural Fields combining deep convolutional neural networks and conditional random fields, trained by maximizing the area under the ROC curve to handle imbalanced ordered and disordered residue distributions.
Topics
Details
- License:
- GPL-3.0
- Cost:
- Free of charge
- Tool Type:
- web application
- Operating Systems:
- Linux
- Programming Languages:
- C++, C
- Added:
- 8/30/2022
- Last Updated:
- 11/24/2024
Operations
Publications
Wang S, Ma J, Xu J. AUCpreD: proteome-level protein disorder prediction by AUC-maximized deep convolutional neural fields. Bioinformatics. 2016;32(17):i672-i679. doi:10.1093/bioinformatics/btw446. PMID:27587688. PMCID:PMC5013916.