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Edward K. Lobenhofer

dblp:74/3352 · DBLP profile ↗
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1ranked-venue papers
0as first author
0since 2021 · last 2003
—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 · 70% Computational science and engineering · 30%

Topics — the 4 heaviest of 4, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › gene expression analysis
gene clustering
0.012003
Gene Selection and Clustering for Time-course and Dose-response Microarray Experiments Using Order-restricted Inference · Bioinform. 2003
Bioinformatics and computational biology
gene expression analysis
0.012003
Gene Selection and Clustering for Time-course and Dose-response Microarray Experiments Using Order-restricted Inference · Bioinform. 2003
Computational science and engineering › statistical computing
order-restricted inference
0.012003
Gene Selection and Clustering for Time-course and Dose-response Microarray Experiments Using Order-restricted Inference · Bioinform. 2003
Bioinformatics and computational biology › gene expression analysis › time-series gene expression analysis
time-course microarray analysis
0.012003
Gene Selection and Clustering for Time-course and Dose-response Microarray Experiments Using Order-restricted Inference · Bioinform. 2003

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

order-restricted inference · 0.0bootstrap · 0.0
YearPublicationVenuePosition
2003 Gene Selection and Clustering for Time-course and Dose-response Microarray Experiments Using Order-restricted Inference
abstract
We propose an algorithm for selecting and clustering genes according to their time-course or dose-response profiles using gene expression data. The proposed algorithm is based on the order-restricted inference methodology developed in statistics. We describe the methodology for time-course experiments although it is applicable to any ordered set of treatments. Candidate temporal profiles are defined in terms of inequalities among mean expression levels at the time points. The proposed algorithm selects genes when they meet a bootstrap-based criterion for statistical significance and assigns each selected gene to the best fitting candidate profile. We illustrate the methodology using data from a cDNA microarray experiment in which a breast cancer cell line was stimulated with estrogen for different time intervals. In this example, our method was able to identify several biologically interesting genes that previous analyses failed to reveal.
Shyamal D. Peddada, Edward K. Lobenhofer, Leping Li, Cynthia A. Afshari, Clarice R. Weinberg, David M. Umbach
Bioinform.2