High-order neural networks and kernel methods for peptide-MHC binding prediction

0301 basic medicine Support Vector Machine Molecular Sequence Data Major Histocompatibility Complex Epitopes 03 medical and health sciences ROC Curve Area Under Curve Humans Amino Acid Sequence Neural Networks, Computer Databases, Protein Peptides Algorithms Protein Binding
DOI: 10.1093/bioinformatics/btv371 Publication Date: 2015-07-24T00:53:42Z
ABSTRACT
Abstract Motivation: Effective computational methods for peptide-protein binding prediction can greatly help clinical peptide vaccine search and design. However, previous computational methods fail to capture key nonlinear high-order dependencies between different amino acid positions. As a result, they often produce low-quality rankings of strong binding peptides. To solve this problem, we propose nonlinear high-order machine learning methods including high-order neural networks (HONNs) with possible deep extensions and high-order kernel support vector machines to predict major histocompatibility complex-peptide binding. Results: The proposed high-order methods improve quality of binding predictions over other prediction methods. With the proposed methods, a significant gain of up to 25–40% is observed on the benchmark and reference peptide datasets and tasks. In addition, for the first time, our experiments show that pre-training with high-order semi-restricted Boltzmann machines significantly improves the performance of feed-forward HONNs. Moreover, our experiments show that the proposed shallow HONN outperform the popular pre-trained deep neural network on most tasks, which demonstrates the effectiveness of modelling high-order feature interactions for predicting major histocompatibility complex-peptide binding. Availability and implementation: There is no associated distributable software. Contact:  renqiang@nec-labs.com or mark.gerstein@yale.edu Supplementary information: Supplementary data are available at Bioinformatics online.
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