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Karen Willbrand

dblp:96/5756 · DBLP profile ↗
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2ranked-venue papers
1as first author
0since 2021 · last 2006
—ORCID · none

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 2 · 1 first-author

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
2 papers
Bioinformatics and computational biology · 77% Computational science and engineering · 23%

Topics — the 3 heaviest of 3, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology
gene expression analysis
0.122006
Unbiased pattern detection in microarray data series · Bioinform. 2006
Identifying genes from up-down properties of microarray expression series · Bioinform. 2005
Bioinformatics and computational biology › gene expression analysis › time-series gene expression analysis
time-course microarray analysis
0.112006
Unbiased pattern detection in microarray data series · Bioinform. 2006
Computational science and engineering
pattern recognition
0.112005
Identifying genes from up-down properties of microarray expression series · Bioinform. 2005

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

kolmogorov complexity · 0.1compression-based pattern detection · 0.1up-down sequence analysis · 0.1
YearPublicationVenuePosition
2006 Unbiased pattern detection in microarray data series
abstract
MOTIVATION: Following the advent of microarray technology in recent years, the challenge for biologists is to identify genes of interest from the thousands of genetic expression levels measured in each microarray experiment. In many cases the aim is to identify pattern in the data series generated by successive microarray measurements. RESULTS: Here we introduce a new method of detecting pattern in microarray data series which is independent of the nature of this pattern. Our approach provides a measure of the algorithmic compressibility of each data series. A series which is significantly compressible is much more likely to result from simple underlying mechanisms than series which are incompressible. Accordingly, the gene associated with a compressible series is more likely to be biologically significant. We test our method on microarray time series of yeast cell cycle and show that it blindly selects genes exhibiting the expected cyclic behaviour as well as detecting other forms of pattern. Our results successfully predict two independent non-microarray experimental studies.
Sebastian E. Ahnert, Karen Willbrand, Francis C. S. Brown, Thomas M. A. Fink
Bioinform.2
2005 Identifying genes from up-down properties of microarray expression series
abstract
MOTIVATION: We consider any collection of microarrays that can be ordered to form a progression; for example, as a function of time, severity of disease or dose of a stimulant. By plotting the expression level of each gene as a function of time, or severity, or dose, we form an expression series, or curve, for each gene. While most of these curves will exhibit random fluctuations, some will contain a pattern, and these are the genes that are most likely associated with the quantity used to order them. RESULTS: We introduce a method of identifying the pattern and hence genes in microarray expression curves without knowing what kind of pattern to look for. Key to our approach is the sequence of ups and downs formed by pairs of consecutive data points in each curve. As a benchmark, we blindly identified genes from yeast cell cycles without selecting for periodic or any other anticipated behaviour. CONTACT: [email protected] SUPPLEMENTARY INFORMATION: The complete versions of Table 2 and Figure 4, as well as other material, can be found at http://www.lps.ens.fr/~willbran/up-down/ or http://www.tcm.phy.cam.ac.uk/~tmf20/up-down/
Karen Willbrand, François Radvanyi, Jean-Pierre Nadal, Jean-Paul Thiery, Thomas M. A. Fink
Bioinform.1