Demonstration venue · read-only. Every page can be browsed; the buttons that would change it are switched off. Create an account to run TaxoReview on your own data. A simulation from public publication records: the people listed were not invited and did not agree to review.
? Tutorial for this page

Gardar Sveinbjörnsson

dblp:120/5154 · DBLP profile ↗
← Back
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

TopicWeightPapersLastEvidence papers
Computational social science and digital humanities
causal inference
0.112012
Causal stability ranking · Bioinform. 2012
Bioinformatics and computational biology
gene expression
0.012012
Causal stability ranking · Bioinform. 2012
Bioinformatics and computational biology › statistical genetics
phenotype prediction
0.012012
Causal stability ranking · Bioinform. 2012

Methods — techniques the papers use, named apart from their topics

regression · 0.1causal effect lower bounds · 0.1
YearPublicationVenuePosition
2012 Causal stability ranking
abstract
Genotypic 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