Demo Data from EDBT 2026 / reviewers in the wild / expert
Gardar Sveinbjörnsson
dblp:120/5154
· DBLP profile ↗
1ranked-venue papers
0as first author
0since 2021 · last 2012
0000-0003-2429-9468ORCID · 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 |
Computational social science and digital humanities · 62% Bioinformatics and computational biology · 38% |
Topics — the 3 heaviest of 3, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Computational social science and digital humanities
causal inference |
0.1 | 1 | 2012 | Causal stability ranking · Bioinform. 2012 |
Bioinformatics and computational biology
gene expression |
0.0 | 1 | 2012 | Causal stability ranking · Bioinform. 2012 |
Bioinformatics and computational biology › statistical genetics
phenotype prediction |
0.0 | 1 | 2012 | Causal stability ranking · Bioinform. 2012 |
Methods — techniques the papers use, named apart from their topics
regression · 0.1causal effect lower bounds · 0.1
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2012 | Causal stability rankingabstractGenotypic causes of a phenotypic trait are typically determined via randomized controlled intervention experiments. Such experiments are often prohibitive with respect to durations and costs, and informative prioritization of experiments is desirable. We therefore consider predicting stable rankings of genes (covariates), according to their total causal effects on a phenotype (response), from observational data. Since causal effects are generally non-identifiable from observational data only, we use a method that can infer lower bounds for the total causal effect under some assumptions. We validated our method, which we call Causal Stability Ranking (CStaR), in two situations. First, we performed knock-out experiments with Arabidopsis thaliana according to a predicted ranking based on observational gene expression data, using flowering time as phenotype of interest. Besides several known regulators of flowering time, we found almost half of the tested top ranking mutants to have a significantly changed flowering time. Second, we compared CStaR to established regression-based methods on a gene expression dataset of Saccharomyces cerevisiae. We found that CStaR outperforms these established methods. Our method allows for efficient design and prioritization of future intervention experiments, and due to its generality it can be used for a broad spectrum of applications. Daniel J. Stekhoven, Izabel Moraes, Gardar Sveinbjörnsson, Lars Hennig, Marloes H. Maathuis, Peter Bühlmann |
Bioinform. | 3 |