Protein secondary structure prediction using deep convolutional neural fields
December 02, 2015 Β· Declared Dead Β· π Scientific Reports
"No code URL or promise found in abstract"
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Authors
Sheng Wang, Jian Peng, Jianzhu Ma, Jinbo Xu
arXiv ID
1512.00843
Category
q-bio.BM
Cross-listed
cs.LG,
q-bio.QM
Citations
533
Venue
Scientific Reports
Last Checked
2 months ago
Abstract
Protein secondary structure (SS) prediction is important for studying protein structure and function. When only the sequence (profile) information is used as input feature, currently the best predictors can obtain ~80% Q3 accuracy, which has not been improved in the past decade. Here we present DeepCNF (Deep Convolutional Neural Fields) for protein SS prediction. DeepCNF is a Deep Learning extension of Conditional Neural Fields (CNF), which is an integration of Conditional Random Fields (CRF) and shallow neural networks. DeepCNF can model not only complex sequence-structure relationship by a deep hierarchical architecture, but also interdependency between adjacent SS labels, so it is much more powerful than CNF. Experimental results show that DeepCNF can obtain ~84% Q3 accuracy, ~85% SOV score, and ~72% Q8 accuracy, respectively, on the CASP and CAMEO test proteins, greatly outperforming currently popular predictors. As a general framework, DeepCNF can be used to predict other protein structure properties such as contact number, disorder regions, and solvent accessibility.
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