Demo Data from EDBT 2026 / reviewers in the wild / expert
K. Felsenstein
dblp:43/9331
· DBLP profile ↗
1ranked-venue papers
0as first author
0since 2021 · last 2011
—ORCID · none
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 › gene expression analysis
microarray data analysis |
0.1 | 1 | 2011 | Biological assessment of robust noise models in microarray data analysis · Bioinform. 2011 |
Bioinformatics and computational biology › gene expression analysis › differential expression analysis
differentially expressed gene identification |
0.0 | 1 | 2011 | Biological assessment of robust noise models in microarray data analysis · Bioinform. 2011 |
Bioinformatics and computational biology
gene expression analysis |
0.0 | 1 | 2011 | Biological assessment of robust noise models in microarray data analysis · Bioinform. 2011 |
Methods — techniques the papers use, named apart from their topics
t-distribution · 0.1hierarchical bayesian analysis of variance · 0.1gaussian mixture model · 0.1
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2011 | Biological assessment of robust noise models in microarray data analysisabstractMOTIVATION: Although several recently proposed analysis packages for microarray data can cope with heavy-tailed noise, many applications rely on Gaussian assumptions. Gaussian noise models foster computational efficiency. This comes, however, at the expense of increased sensitivity to outlying observations. Assessing potential insufficiencies of Gaussian noise in microarray data analysis is thus important and of general interest. RESULTS: We propose to this end assessing different noise models on a large number of microarray experiments. The goodness of fit of noise models is quantified by a hierarchical Bayesian analysis of variance model, which predicts normalized expression values as a mixture of a Gaussian density and t-distributions with adjustable degrees of freedom. Inference of differentially expressed genes is taken into consideration at a second mixing level. For attaining far reaching validity, our investigations cover a wide range of analysis platforms and experimental settings. As the most striking result, we find irrespective of the chosen preprocessing and normalization method in all experiments that a heavy-tailed noise model is a better fit than a simple Gaussian. Further investigations revealed that an appropriate choice of noise model has a considerable influence on biological interpretations drawn at the level of inferred genes and gene ontology terms. We conclude from our investigation that neglecting the over dispersed noise in microarray data can mislead scientific discovery and suggest that the convenience of Gaussian-based modelling should be replaced by non-parametric approaches or other methods that account for heavy-tailed noise. Alexandra Posekany, K. Felsenstein, Peter Sykacek |
Bioinform. | 2 |