Demo Data from EDBT 2026 / reviewers in the wild / expert
Kathryn J. Doroschak
dblp:146/9864
· DBLP profile ↗
1ranked-venue papers
0as first author
0since 2021 · last 2014
0000-0003-4806-5164ORCID · reported
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 2 heaviest of 2, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology › protein function prediction
network-based function prediction |
0.2 | 1 | 2014 | New directions for diffusion-based network prediction of protein function: incorporating pathways with confidence · Bioinform. 2014 |
Bioinformatics and computational biology
protein function prediction |
0.2 | 1 | 2014 | New directions for diffusion-based network prediction of protein function: incorporating pathways with confidence · Bioinform. 2014 |
Methods — techniques the papers use, named apart from their topics
multi-way cut · 0.2majority vote · 0.2functional flow · 0.2diffusion state distance · 0.2
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2014 | New directions for diffusion-based network prediction of protein function: incorporating pathways with confidenceabstractMOTIVATION: It has long been hypothesized that incorporating models of network noise as well as edge directions and known pathway information into the representation of protein-protein interaction (PPI) networks might improve their utility for functional inference. However, a simple way to do this has not been obvious. We find that diffusion state distance (DSD), our recent diffusion-based metric for measuring dissimilarity in PPI networks, has natural extensions that incorporate confidence, directions and can even express coherent pathways by calculating DSD on an augmented graph. RESULTS: We define three incremental versions of DSD which we term cDSD, caDSD and capDSD, where the capDSD matrix incorporates confidence, known directed edges, and pathways into the measure of how similar each pair of nodes is according to the structure of the PPI network. We test four popular function prediction methods (majority vote, weighted majority vote, multi-way cut and functional flow) using these different matrices on the Baker's yeast PPI network in cross-validation. The best performing method is weighted majority vote using capDSD. We then test the performance of our augmented DSD methods on an integrated heterogeneous set of protein association edges from the STRING database. The superior performance of capDSD in this context confirms that treating the pathways as probabilistic units is more powerful than simply incorporating pathway edges independently into the network. AVAILABILITY: All source code for calculating the confidences, for extracting pathway information from KEGG XML files, and for calculating the cDSD, caDSD and capDSD matrices are available from http://dsd.cs.tufts.edu/capdsd Mengfei Cao, Christopher M. Pietras, Xian Feng, Kathryn J. Doroschak, Thomas Schaffner, Lenore Cowen, Benjamin Hescott |
Bioinform. | 4 |