EDBT 2026 Demo / reviewers in the wild / expert
Cristobal G. dos Remedios
dblp:09/878
· DBLP profile ↗
1ranked-venue papers
0as first author
0since 2021 · last 2008
—ORCID · unresolved
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 › gene co-expression analysis
differential coexpression |
0.1 | 1 | 2008 | Differential variability analysis of gene expression and its application to human diseases · ISMB 2008 |
Bioinformatics and computational biology › gene expression analysis
differential variability analysis |
0.1 | 1 | 2008 | Differential variability analysis of gene expression and its application to human diseases · ISMB 2008 |
Bioinformatics and computational biology
gene expression analysis |
0.1 | 1 | 2008 | Differential variability analysis of gene expression and its application to human diseases · ISMB 2008 |
Methods — techniques the papers use, named apart from their topics
statistical testing · 0.1microarray preprocessing · 0.1
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2008 | Differential variability analysis of gene expression and its application to human diseasesabstractMOTIVATION: Current microarray analyses focus on identifying sets of genes that are differentially expressed (DE) or differentially coexpressed (DC) in different biological states (e.g. diseased versus non-diseased). We observed that in many human diseases, some genes have a significant increase or decrease in expression variability (variance). As these observed changes in expression variability may be caused by alteration of the underlying expression dynamics, such differential variability (DV) patterns are also biologically interesting. RESULTS: Here we propose a novel analysis for changes in gene expression variability between groups of samples, which we call differential variability analysis. We introduce the concept of differential variability (DV), and present a simple procedure for identifying DV genes from microarray data. Our procedure is evaluated with simulated and real microarray datasets. The effect of data preprocessing methods on identification of DV gene is investigated. The biological significance of DV analysis is demonstrated with four human disease datasets. The relationships among DV, DE and DC genes are investigated. The results suggest that changes in expression variability are associated with changes in coexpression pattern, which imply that DV is not merely stochastic noise, but informative signal. AVAILABILITY: The R source code for differential variability analysis is available from the contact authors upon request. Joshua W. K. Ho, Maurizio Stefani, Cristobal G. dos Remedios, Michael A. Charleston |
ISMB | 3 |