Demo Data from SIGIR 2026 / reviewers in the wild / expert
Caterine Ikae
dblp:117/4873
· DBLP profile ↗
1ranked-venue papers
0as first author
0since 2021 · last 2012
—ORCID · none
Domains — the database's venue-derived domains; a paper can count in several
Artificial intelligence and machine learning · 1Graphics, computer vision, multimedia, augmented reality and games · 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 · 50% Medical and health informatics · 50% | |
| Artificial intelligence
1 paper |
Image recognition and object detection · 100% |
Topics — the 1 heaviest of 4, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology › systems bioinformatics
disease modeling |
0.1 | 1 | 2012 | Coupling Spatiotemporal Disease Modeling with Diagnosis · AAAI 2012 |
Methods — techniques the papers use, named apart from their topics
state space model · 0.3computer vision · 0.3
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2012 | Coupling Spatiotemporal Disease Modeling with DiagnosisabstractModelling the density of an infectious disease in space and time is a task generally carried out separately from the diagnosis of that disease in individuals. These two inference problems are complementary, however: diagnosis of disease can be done more accurately if prior information from a spatial risk model is employed, and in turn a disease density model can benefit from the incorporation of rich symptomatic information rather than simple counts of presumed cases of infection. We propose a unifying framework for both of these tasks, and illustrate it with the case of malaria. To do this we first introduce a state space model of malaria spread, and secondly a computer vision based system for detecting plasmodium in microscopical blood smear images, which can be run on location-aware mobile devices. We demonstrate the tractability of combining both elements and the improvement in accuracy this brings about. Martin Gordon Mubangizi, Caterine Ikae, Athina Spiliopoulou, John A. Quinn |
AAAI | 2 |