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René Korn

dblp:00/2930 · DBLP profile ↗
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2ranked-venue papers
1as first author
0since 2021 · last 2013
0000-0002-3708-7272ORCID · reported

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

Artificial intelligence and machine learning · 1Applied, interdisciplinary, general and emerging computing · 1 · 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
1 paper
Bioinformatics and computational biology · 100%

Topics — the 1 heaviest of 2, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › gene expression analysis
gene expression data mining
0.112005
Common denominator procedure: a novel approach to gene-expression data mining for identification of phenotype-specific genes · Bioinform. 2005

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

common denominator procedure · 0.1
YearPublicationVenuePosition
2013 Automated delineation of lung tumors from CT images using a single click ensemble segmentation approach
Yuhua Gu, Lawrence O. Hall, Dmitry B. Goldgof, Ching-Yen Li, René Korn, Claus Bendtsen, Emmanuel Rios Velazquez, Andre Dekker, Hugo J. W. L. Aerts, Philippe Lambin, Xiuli Li, Robert A. Gatenby, Robert J. Gillies
Pattern Recognit.6
2005 Common denominator procedure: a novel approach to gene-expression data mining for identification of phenotype-specific genes
abstract
MOTIVATION: We have established a novel data mining procedure for the identification of genes associated with pre-defined phenotypes and/or molecular pathways. Based on the observation that these genes are frequently expressed in the same place or in close proximity at about the same time, we have devised an approach termed Common Denominator Procedure. One unusual feature of this approach is that the specificity and probability to identify genes linked to the desired phenotype/pathway increase with greater diversity of the input data. RESULT: To show the feasibility of our approach, the Cancer Genome Anatomy Project expression data combined with a defined set of angiogenic factors was used to identify additional and novel angiogenesis-associated genes. A multitude of these additional genes were known to be associated with angiogenesis according to published data, verifying our approach. For some of the remaining candidate genes, application of a high-throughput functional genomics platform (XantoScreen) provided further experimental evidence for association with angiogenesis.
René Korn, Sascha Röhrig, Steffen Schulze-Kremer, Ulrich Brinkmann
Bioinform.1