VLDB 2026 Research / reviewers in the wild / expert
Jeffrey C. Boyington
dblp:118/0859
· DBLP profile ↗
1ranked-venue papers
0as first author
0since 2021 · last 2012
—ORCID · unresolved
Domains — the database's venue-derived domains; a paper can count in several
Applied, interdisciplinary, general and emerging computing · 1
Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.
| Interdisciplinary, comprehensive, and emerging computing
1 paper |
Bioinformatics and computational biology · 100% |
Topics — the 3 heaviest of 3, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology › proteomics
post-translational modification prediction |
0.1 | 1 | 2012 | Computational prediction of N-linked glycosylation incorporating structural properties and patterns · Bioinform. 2012 |
Bioinformatics and computational biology
protein structure analysis |
0.0 | 1 | 2012 | Computational prediction of N-linked glycosylation incorporating structural properties and patterns · Bioinform. 2012 |
Bioinformatics and computational biology › protein structure analysis
structural feature extraction |
0.0 | 1 | 2012 | Computational prediction of N-linked glycosylation incorporating structural properties and patterns · Bioinform. 2012 |
Methods — techniques the papers use, named apart from their topics
random forest · 0.110-fold cross-validation · 0.1
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2012 | Computational prediction of N-linked glycosylation incorporating structural properties and patternsabstractMOTIVATION: N-linked glycosylation occurs predominantly at the N-X-T/S motif, where X is any amino acid except proline. Not all N-X-T/S sequons are glycosylated, and a number of web servers for predicting N-linked glycan occupancy using sequence and/or residue pattern information have been developed. None of the currently available servers, however, utilizes protein structural information for the prediction of N-glycan occupancy. RESULTS: Here, we describe a novel classifier algorithm, NGlycPred, for the prediction of glycan occupancy at the N-X-T/S sequons. The algorithm utilizes both structural as well as residue pattern information and was trained on a set of glycosylated protein structures using the Random Forest algorithm. The best predictor achieved a balanced accuracy of 0.687 under 10-fold cross-validation on a curated dataset of 479 N-X-T/S sequons and outperformed sequence-based predictors when evaluated on the same dataset. The incorporation of structural information, including local contact order, surface accessibility/composition and secondary structure thus improves the prediction accuracy of glycan occupancy at the N-X-T/S consensus sequon. AVAILABILITY AND IMPLEMENTATION: NGlycPred is freely available to non-commercial users as a web-based server at http://exon.niaid.nih.gov/nglycpred/. Gwo-Yu Chuang, Jeffrey C. Boyington, M. Gordon Joyce, Gary J. Nabel, Peter D. Kwong, Ivelin Georgiev |
Bioinform. | 2 |